Job Search Results for pharmaceutical
May 08, 2026
Hayward, CA
|
Pharmacist
|
Contract,Perm Possible
|
$40 - $50 (hourly estimate)
{"JobID":528213,"JobType":["Contract,Perm Possible"],"EmployerID":null,"Location":{"Latitude":-122.11,"Longitude":37.62,"Distance":null},"State":"California","Zip":"94545","ReferenceID":"SFR-46b93c53-e4c1-4210-a0da-7e776a1d4546","PostedDate":"\/Date(1778244933000)\/","Description":"we power the future of consumer healthcare. We started in 2016 with a visionto modernize healthcare. We provide the building blocks needed to launch and scaleworld-class healthcare experiences.With millions of prescriptions shipped and millions of patients served, we work with manyof the world?s largest healthcare organizations - including payers, providers, life sciencescompanies, and consumer health brands. And with new partners continually joining ourmission, we aim to further shape the future of healthcare - one patient at a time.We?re so glad you?re here. Let?s build something great together.Aboutthe RoleThe Staff Pharmacist reports to the Pharmacist in Charge to support our Pharmacy Operations team. You will be responsible for verifying prescriptions (RX image to data entry remotely).As a Staff Pharmacist with Truepill, you will play a key role in ensuring the delivery of high-quality pharmaceuticalservices, and maintaining regulatory compliance.Why You?ll Love Working at Truepill?? We put patients first ? We put patients first because their well-being is ourpriority.? We are curious ? We never settle for how it?s done today. We invent how it will bedone tomorrow. Because we don?t just ask ?why??, we ask ?why not??.? We have impact with urgency ? We?re the spark that ignites positive change inhealthcare. We create impact because we don?t anticipate; we innovate.? We lead with Integrity ? Leading with integrity is the foundation of trust. Wealways do what?s best for our people, our customers, and above all, our patients.? We hold customer confidentiality ? We put discretion \u0026 confidentiality at theheart of every relationship.You?re excited about this opportunity because?? You will maintain appropriate documentation for services rendered, including prescription records and patient profiles.? You?ll coordinate the provision of pharmaceutical services and the delivery ofmedications and products to patients.? You will ensure the security of legend drugs and adherence to regulatorystandards.? You will participate in the quality assurance program to maintain and improvepharmacy operations.? You will maintain patient confidentiality with medication profiles and sensitiveinformation.? You?ll collaborate with cross-functional teams to support organizational goals andinitiatives.? Your daily duties will include patient consultations, prescription verification, anddrug utilization review? You have an active, clear, and unrestricted Pharmacist license within the state ofNew York.? You are a Registered Pharmacist and in good standing with the Board of Pharmacy.? You have a Bachelor?s degree in Pharmacy or Pharm D degree.? You possess a minimum of 1 year of pharmacy experience, preferably in a clinicalsetting.? You have the ability and willingness to work at a computer screen for long periodsif needed.? You have demonstrated excellent leadership and organizational skills to effectivelymanage pharmacy operations.? You display a commitment to patient-centered care and adherence to ethicalstandards.? You have strong communication skills and the ability to work collaboratively in ateam environmentWe are a company committed to creating diverse and inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity/affirmative action employer that believes everyone matters. Qualified candidates will receive consideration for employment regardless of their race, color, ethnicity, religion, sex (including pregnancy), sexual orientation, gender identity and expression, marital status, national origin, ancestry, genetic factors, age, disability, protected veteran status, military or uniformed service member status, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or recruiting process, please send a request to HR@insightglobal.com.To learn more about how we collect, keep, and process your private information, please review Insight Global\u0027s Workforce Privacy Policy: https://insightglobal.com/workforce-privacy-policy/.","Title":"Remote Pharmacist - NY","City":"Hayward","ExpirationDate":null,"PriorityOrder":0,"Requirements":"? You have an active, clear, and unrestricted Pharmacist license within the state ofNew York.? You are a Registered Pharmacist and in good standing with the Board of Pharmacy.? You have a Bachelor?s degree in Pharmacy or Pharm D degree.? You possess a minimum of 1 year of pharmacy experience, preferably in a clinicalsetting.? You have the ability and willingness to work at a computer screen for long periodsif needed.? You have demonstrated excellent leadership and organizational skills to effectivelymanage pharmacy operations.? You display a commitment to patient-centered care and adherence to ethicalstandards.? You have strong communication skills and the ability to work collaboratively in ateam environment","Skills":"","Industry":"Pharmacist","Country":"US","Division":"IT","Office":null,"IsRemoteJob":true,"IsInternalJob":false,"ExtraValues":null,"__RecordIndex":0,"__OrdinalPosition":0,"__Timestamp":0,"Status":null,"ApplicantCount":0,"SubmittalCount":0,"ApplicationToHireRatio":0,"JobDuration":null,"SalaryHigh":50.0000,"SalaryLow":40.0000,"PayRateOvertime":0,"PayRateStraight":0,"Filled":0,"RemainingOpenings":0,"TotalOpenings":0,"Visa":null,"ClearanceType":null,"IsClearanceRequired":false,"IsHealthcare":false,"IsRemote":false,"EndClient":null,"JobCreatedDate":"\/Date(-62135578800000)\/","JobModifiedDate":"\/Date(-62135578800000)\/"}
we power the future of consumer healthcare. We started in 2016 with a visionto modernize healthcare. We provide the building blocks needed to launch and scaleworld-class healthcare experiences.With... millions of prescriptions shipped and millions of patients served, we work with manyof the world?s largest healthcare organizations - including payers, providers, life sciencescompanies, and consumer health brands. And with new partners continually joining ourmission, we aim to further shape the future of healthcare - one patient at a time.We?re so glad you?re here. Let?s build something great together.Aboutthe RoleThe Staff Pharmacist reports to the Pharmacist in Charge to support our Pharmacy Operations team. You will be responsible for verifying prescriptions (RX image to data entry remotely).As a Staff Pharmacist with Truepill, you will play a key role in ensuring the delivery of high-quality pharmaceuticalservices, and maintaining regulatory compliance.Why You?ll Love Working at Truepill?? We put patients first ? We put patients first because their well-being is ourpriority.? We are curious ? We never settle for how it?s done today. We invent how it will bedone tomorrow. Because we don?t just ask ?why??, we ask ?why not??.? We have impact with urgency ? We?re the spark that ignites positive change inhealthcare. We create impact because we don?t anticipate; we innovate.? We lead with Integrity ? Leading with integrity is the foundation of trust. Wealways do what?s best for our people, our customers, and above all, our patients.? We hold customer confidentiality ? We put discretion & confidentiality at theheart of every relationship.You?re excited about this opportunity because?? You will maintain appropriate documentation for services rendered, including prescription records and patient profiles.? You?ll coordinate the provision of pharmaceutical services and the delivery ofmedications and products to patients.? You will ensure the security of legend drugs and adherence to regulatorystandards.? You will participate in the quality assurance program to maintain and improvepharmacy operations.? You will maintain patient confidentiality with medication profiles and sensitiveinformation.? You?ll collaborate with cross-functional teams to support organizational goals andinitiatives.? Your daily duties will include patient consultations, prescription verification, anddrug utilization review? You have an active, clear, and unrestricted Pharmacist license within the state ofNew York.? You are a Registered Pharmacist and in good standing with the Board of Pharmacy.? You have a Bachelor?s degree in Pharmacy or Pharm D degree.? You possess a minimum of 1 year of pharmacy experience, preferably in a clinicalsetting.? You have the ability and willingness to work at a computer screen for long periodsif needed.? You have demonstrated excellent leadership and organizational skills to effectivelymanage pharmacy operations.? You display a commitment to patient-centered care and adherence to ethicalstandards.? You have strong communication skills and the ability to work collaboratively in ateam environmentWe are a company committed to creating diverse and inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity/affirmative action employer that believes everyone matters. Qualified candidates will receive consideration for employment regardless of their race, color, ethnicity, religion, sex (including pregnancy), sexual orientation, gender identity and expression, marital status, national origin, ancestry, genetic factors, age, disability, protected veteran status, military or uniformed service member status, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or recruiting process, please send a request to HR@insightglobal.com.To learn more about how we collect, keep, and process your private information, please review Insight Global's Workforce Privacy Policy: https://insightglobal.com/workforce-privacy-policy/.
May 11, 2026
Leawood, KS
|
Designer
|
Contract
|
$46 - $57 (hourly estimate)
{"JobID":528780,"JobType":["Contract"],"EmployerID":null,"Location":{"Latitude":-94.68,"Longitude":38.9,"Distance":null},"State":"Kansas","Zip":"66211","ReferenceID":"KCM-fadcb2f9-c3cb-4bab-830c-473cba99960a","PostedDate":"\/Date(1778505735000)\/","Description":"The Piping Designer will be responsible for the design, layout, and modeling of piping systems for power plant and energy-related facilities. This role works closely with engineers, project managers, and other designers to develop accurate, constructible designs that meet project specifications, codes, and quality standards. The ideal candidate is detail-oriented, collaborative, and experienced in 3D modeling and piping system design.Key Responsibilities- Design and route piping systems and layouts for power plant and industrial energy systems- Develop and maintain 3D models of piping and related equipment using industry-standard design software- Plan and produce detailed drawings for production, including design layouts, problem analysis, and required calculations- Perform quality checks of 3D models to identify interferences and improve constructability- Resolve comments from internal and external drawing reviews and implement feedback efficiently- Complete as-built drawings using RFIs, ECNs, and red-lined markups to generate accurate Conformed to Construction Records- Coordinate with engineering and project teams to ensure designs meet project schedules and technical requirements- Adhere to drafting standards, design procedures, and quality control processesWe are a company committed to creating diverse and inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity/affirmative action employer that believes everyone matters. Qualified candidates will receive consideration for employment regardless of their race, color, ethnicity, religion, sex (including pregnancy), sexual orientation, gender identity and expression, marital status, national origin, ancestry, genetic factors, age, disability, protected veteran status, military or uniformed service member status, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or recruiting process, please send a request to HR@insightglobal.com.To learn more about how we collect, keep, and process your private information, please review Insight Global\u0027s Workforce Privacy Policy: https://insightglobal.com/workforce-privacy-policy/.","Title":"Piping Designer","City":"Leawood","ExpirationDate":null,"PriorityOrder":0,"Requirements":"- 10+ years of experience as a Piping Designer? Layouts, isometrics, routing- Plant3D software experience- Experience must be in Power, Oil \u0026 Gas, Petrochemical or Pharmaceutical","Skills":"- Experience with P\u0026ID\u0027s","Industry":"Designer","Country":"US","Division":"AF\u0026E","Office":null,"IsRemoteJob":true,"IsInternalJob":false,"ExtraValues":null,"__RecordIndex":0,"__OrdinalPosition":0,"__Timestamp":0,"Status":null,"ApplicantCount":0,"SubmittalCount":0,"ApplicationToHireRatio":0,"JobDuration":null,"SalaryHigh":57.0000,"SalaryLow":45.6000,"PayRateOvertime":0,"PayRateStraight":0,"Filled":0,"RemainingOpenings":0,"TotalOpenings":0,"Visa":null,"ClearanceType":null,"IsClearanceRequired":false,"IsHealthcare":false,"IsRemote":false,"EndClient":null,"JobCreatedDate":"\/Date(-62135578800000)\/","JobModifiedDate":"\/Date(-62135578800000)\/"}
The Piping Designer will be responsible for the design, layout, and modeling of piping systems for power plant and energy-related facilities. This role works closely with engineers, project managers,... and other designers to develop accurate, constructible designs that meet project specifications, codes, and quality standards. The ideal candidate is detail-oriented, collaborative, and experienced in 3D modeling and piping system design.Key Responsibilities- Design and route piping systems and layouts for power plant and industrial energy systems- Develop and maintain 3D models of piping and related equipment using industry-standard design software- Plan and produce detailed drawings for production, including design layouts, problem analysis, and required calculations- Perform quality checks of 3D models to identify interferences and improve constructability- Resolve comments from internal and external drawing reviews and implement feedback efficiently- Complete as-built drawings using RFIs, ECNs, and red-lined markups to generate accurate Conformed to Construction Records- Coordinate with engineering and project teams to ensure designs meet project schedules and technical requirements- Adhere to drafting standards, design procedures, and quality control processesWe are a company committed to creating diverse and inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity/affirmative action employer that believes everyone matters. Qualified candidates will receive consideration for employment regardless of their race, color, ethnicity, religion, sex (including pregnancy), sexual orientation, gender identity and expression, marital status, national origin, ancestry, genetic factors, age, disability, protected veteran status, military or uniformed service member status, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or recruiting process, please send a request to HR@insightglobal.com.To learn more about how we collect, keep, and process your private information, please review Insight Global's Workforce Privacy Policy: https://insightglobal.com/workforce-privacy-policy/.
Mar 24, 2026
Leawood, KS
|
Designer
|
Contract
|
$46 - $57 (hourly estimate)
{"JobID":510403,"JobType":["Contract"],"EmployerID":null,"Location":{"Latitude":-94.68,"Longitude":38.9,"Distance":null},"State":"Kansas","Zip":"66211","ReferenceID":"KCM-f7e09127-5752-4f69-a8a6-10d3ca9f40db","PostedDate":"\/Date(1774376728000)\/","Description":"The Piping Designer will be responsible for the design, layout, and modeling of piping systems for power plant and energy-related facilities. This role works closely with engineers, project managers, and other designers to develop accurate, constructible designs that meet project specifications, codes, and quality standards. The ideal candidate is detail-oriented, collaborative, and experienced in 3D modeling and piping system design.Key Responsibilities- Design and route piping systems and layouts for power plant and industrial energy systems- Develop and maintain 3D models of piping and related equipment using industry-standard design software- Plan and produce detailed drawings for production, including design layouts, problem analysis, and required calculations- Perform quality checks of 3D models to identify interferences and improve constructability- Resolve comments from internal and external drawing reviews and implement feedback efficiently- Complete as-built drawings using RFIs, ECNs, and red-lined markups to generate accurate Conformed to Construction Records- Coordinate with engineering and project teams to ensure designs meet project schedules and technical requirements- Adhere to drafting standards, design procedures, and quality control processesWe are a company committed to creating diverse and inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity/affirmative action employer that believes everyone matters. Qualified candidates will receive consideration for employment regardless of their race, color, ethnicity, religion, sex (including pregnancy), sexual orientation, gender identity and expression, marital status, national origin, ancestry, genetic factors, age, disability, protected veteran status, military or uniformed service member status, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or recruiting process, please send a request to HR@insightglobal.com.To learn more about how we collect, keep, and process your private information, please review Insight Global\u0027s Workforce Privacy Policy: https://insightglobal.com/workforce-privacy-policy/.","Title":"Piping Designer","City":"Leawood","ExpirationDate":null,"PriorityOrder":0,"Requirements":"- 10+ years of experience as a Piping Designer? Layouts, isometrics, routing- Plant3D software experience- Experience must be in Power, Oil \u0026 Gas, Petrochemical or Pharmaceutical","Skills":"- Experience with P\u0026ID\u0027s","Industry":"Designer","Country":"US","Division":"AF\u0026E","Office":null,"IsRemoteJob":true,"IsInternalJob":false,"ExtraValues":null,"__RecordIndex":0,"__OrdinalPosition":0,"__Timestamp":0,"Status":null,"ApplicantCount":0,"SubmittalCount":0,"ApplicationToHireRatio":0,"JobDuration":null,"SalaryHigh":57.0000,"SalaryLow":45.6000,"PayRateOvertime":0,"PayRateStraight":0,"Filled":0,"RemainingOpenings":0,"TotalOpenings":0,"Visa":null,"ClearanceType":null,"IsClearanceRequired":false,"IsHealthcare":false,"IsRemote":false,"EndClient":null,"JobCreatedDate":"\/Date(-62135578800000)\/","JobModifiedDate":"\/Date(-62135578800000)\/"}
The Piping Designer will be responsible for the design, layout, and modeling of piping systems for power plant and energy-related facilities. This role works closely with engineers, project managers,... and other designers to develop accurate, constructible designs that meet project specifications, codes, and quality standards. The ideal candidate is detail-oriented, collaborative, and experienced in 3D modeling and piping system design.Key Responsibilities- Design and route piping systems and layouts for power plant and industrial energy systems- Develop and maintain 3D models of piping and related equipment using industry-standard design software- Plan and produce detailed drawings for production, including design layouts, problem analysis, and required calculations- Perform quality checks of 3D models to identify interferences and improve constructability- Resolve comments from internal and external drawing reviews and implement feedback efficiently- Complete as-built drawings using RFIs, ECNs, and red-lined markups to generate accurate Conformed to Construction Records- Coordinate with engineering and project teams to ensure designs meet project schedules and technical requirements- Adhere to drafting standards, design procedures, and quality control processesWe are a company committed to creating diverse and inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity/affirmative action employer that believes everyone matters. Qualified candidates will receive consideration for employment regardless of their race, color, ethnicity, religion, sex (including pregnancy), sexual orientation, gender identity and expression, marital status, national origin, ancestry, genetic factors, age, disability, protected veteran status, military or uniformed service member status, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or recruiting process, please send a request to HR@insightglobal.com.To learn more about how we collect, keep, and process your private information, please review Insight Global's Workforce Privacy Policy: https://insightglobal.com/workforce-privacy-policy/.
Jul 02, 2025
Wilmington, NC
|
Medical Writer
|
Contract
|
$17 - $21 (hourly estimate)
{"JobID":424714,"JobType":["Contract"],"EmployerID":null,"Location":{"Latitude":-77.91,"Longitude":34.21,"Distance":null},"State":"North Carolina","Zip":"28401","ReferenceID":"PHL-f3ce624e-8cb0-4ff4-a605-c5571d4cb8c6","PostedDate":"\/Date(1751484580000)\/","Description":"Our digital advertising client is looking to hire a Copyeditor in LATAM to service their clients. They will be responsible for the basics of copyediting including: performing thorough grammar and spelling checks, review all copy for clarity and logical flow, using a multi-pass approach to catch different error types. They will also be responsible for content accuracy \u0026 style compliance including; ensuring correct spelling of all brand names, companies, products, places, and personal names. Verifying all dates are correct and match their day of the week (e.g., \"Friday, September 9\"). Applying correct AMA (American Medical Association) style throughout. Additionally will ensure formatting consistency across:oHeadlines, subheads, bullet points, and spacing.oSlide notes (in PowerPoint decks), ensuring relevancy and correctness.?Check employee titles where mentioned; confirm via Microsoft Teams or email if unclear.?Review and resolve formatting issues such as widows, orphans, and bullet alignment.We are a company committed to creating diverse and inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity/affirmative action employer that believes everyone matters. Qualified candidates will receive consideration for employment regardless of their race, color, ethnicity, religion, sex (including pregnancy), sexual orientation, gender identity and expression, marital status, national origin, ancestry, genetic factors, age, disability, protected veteran status, military or uniformed service member status, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or recruiting process, please send a request to HR@insightglobal.com.To learn more about how we collect, keep, and process your private information, please review Insight Global\u0027s Workforce Privacy Policy: https://insightglobal.com/workforce-privacy-policy/.","Title":"INTL IT Copyeditor","City":"Wilmington","ExpirationDate":null,"PriorityOrder":0,"Requirements":"?5+ years of copy editing or proofreading experience.?Experience working on PowerPoint presentations and editorial QA of corporate or healthcare materials.?Excellent command of written English and editorial best practices.?High attention to detail and a methodical approach to reviewing documents.?Ability to work independently and under tight deadlines.?Availability for flexible, quick-turnaround assignments.","Skills":"?Strong knowledge of AMA style guidelines.?Experience working with or for healthcare or pharmaceutical companies.","Industry":"Medical Writer","Country":"US","Division":"IT","Office":null,"IsRemoteJob":true,"IsInternalJob":false,"ExtraValues":null,"__RecordIndex":0,"__OrdinalPosition":0,"__Timestamp":0,"Status":null,"ApplicantCount":0,"SubmittalCount":0,"ApplicationToHireRatio":0,"JobDuration":null,"SalaryHigh":21.0000,"SalaryLow":16.8000,"PayRateOvertime":0,"PayRateStraight":0,"Filled":0,"RemainingOpenings":0,"TotalOpenings":0,"Visa":null,"ClearanceType":null,"IsClearanceRequired":false,"IsHealthcare":false,"IsRemote":false,"EndClient":null,"JobCreatedDate":"\/Date(-62135578800000)\/","JobModifiedDate":"\/Date(-62135578800000)\/"}
Our digital advertising client is looking to hire a Copyeditor in LATAM to service their clients. They will be responsible for the basics of copyediting including: performing thorough grammar and... spelling checks, review all copy for clarity and logical flow, using a multi-pass approach to catch different error types. They will also be responsible for content accuracy & style compliance including; ensuring correct spelling of all brand names, companies, products, places, and personal names. Verifying all dates are correct and match their day of the week (e.g., "Friday, September 9"). Applying correct AMA (American Medical Association) style throughout. Additionally will ensure formatting consistency across:oHeadlines, subheads, bullet points, and spacing.oSlide notes (in PowerPoint decks), ensuring relevancy and correctness.?Check employee titles where mentioned; confirm via Microsoft Teams or email if unclear.?Review and resolve formatting issues such as widows, orphans, and bullet alignment.We are a company committed to creating diverse and inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity/affirmative action employer that believes everyone matters. Qualified candidates will receive consideration for employment regardless of their race, color, ethnicity, religion, sex (including pregnancy), sexual orientation, gender identity and expression, marital status, national origin, ancestry, genetic factors, age, disability, protected veteran status, military or uniformed service member status, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or recruiting process, please send a request to HR@insightglobal.com.To learn more about how we collect, keep, and process your private information, please review Insight Global's Workforce Privacy Policy: https://insightglobal.com/workforce-privacy-policy/.
Feb 19, 2026
Irvine, CA
|
Administrative Assistant
|
Contract
|
$41 - $51 (hourly estimate)
{"JobID":496915,"JobType":["Contract"],"EmployerID":null,"Location":{"Latitude":-117.73,"Longitude":33.67,"Distance":null},"State":"California","Zip":"92618","ReferenceID":"OCC-23bd5b2c-eca5-42dc-abdd-fdef7eb3bdc5","PostedDate":"\/Date(1771514911000)\/","Description":"A large medical device company in Irvine, CA is looking for a HYBRID Clinical Research Specialist. This candidate will play a crucial role in supporting a 10 year post market clinical trial for breast implants. Their key responsibilities will include monitoring clinical studies, data verification, regulatory compliance, study documentation, site visits and coordination, and developing written travel reports.We are a company committed to creating diverse and inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity/affirmative action employer that believes everyone matters. Qualified candidates will receive consideration for employment regardless of their race, color, ethnicity, religion, sex (including pregnancy), sexual orientation, gender identity and expression, marital status, national origin, ancestry, genetic factors, age, disability, protected veteran status, military or uniformed service member status, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or recruiting process, please send a request to HR@insightglobal.com.To learn more about how we collect, keep, and process your private information, please review Insight Global\u0027s Workforce Privacy Policy: https://insightglobal.com/workforce-privacy-policy/.","Title":"Clinical Research Specialist","City":"Irvine","ExpirationDate":null,"PriorityOrder":0,"Requirements":"3+ years of experience as a clinical research specialist/associate or field monitor coming from a background of a large research institution, a sponsor company(medical device / biotechnology / pharmaceutical company) , or a hospital3+ years of experience working on a clinical trial Bachelor\u0027s DegreeResiding in the mid west / south region of the USTravel 50%-65%","Skills":"Experience with Class III medical deviceExperience co monitoring / co shadowing a CROExperience with vendor managementExperience with research na?ve sitesExperience with long term study retention of subjects","Industry":"Administrative Assistant","Country":"US","Division":"AF\u0026E","Office":null,"IsRemoteJob":true,"IsInternalJob":false,"ExtraValues":null,"__RecordIndex":0,"__OrdinalPosition":0,"__Timestamp":0,"Status":null,"ApplicantCount":0,"SubmittalCount":0,"ApplicationToHireRatio":0,"JobDuration":null,"SalaryHigh":51.0000,"SalaryLow":40.8000,"PayRateOvertime":0,"PayRateStraight":0,"Filled":0,"RemainingOpenings":0,"TotalOpenings":0,"Visa":null,"ClearanceType":null,"IsClearanceRequired":false,"IsHealthcare":false,"IsRemote":false,"EndClient":null,"JobCreatedDate":"\/Date(-62135578800000)\/","JobModifiedDate":"\/Date(-62135578800000)\/"}
A large medical device company in Irvine, CA is looking for a HYBRID Clinical Research Specialist. This candidate will play a crucial role in supporting a 10 year post market clinical trial for... breast implants. Their key responsibilities will include monitoring clinical studies, data verification, regulatory compliance, study documentation, site visits and coordination, and developing written travel reports.We are a company committed to creating diverse and inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity/affirmative action employer that believes everyone matters. Qualified candidates will receive consideration for employment regardless of their race, color, ethnicity, religion, sex (including pregnancy), sexual orientation, gender identity and expression, marital status, national origin, ancestry, genetic factors, age, disability, protected veteran status, military or uniformed service member status, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or recruiting process, please send a request to HR@insightglobal.com.To learn more about how we collect, keep, and process your private information, please review Insight Global's Workforce Privacy Policy: https://insightglobal.com/workforce-privacy-policy/.
Mar 16, 2026
New York, NY
|
Data Warehousing
|
Contract
|
$10 - $12 (hourly estimate)
{"JobID":507198,"JobType":["Contract"],"EmployerID":null,"Location":{"Latitude":-73.99,"Longitude":40.71,"Distance":null},"State":"New York","Zip":"10016","ReferenceID":"DGH-b3146e5c-202a-4847-8490-e4fdaa1b2375","PostedDate":"\/Date(1773695657000)\/","Description":"Insight Global is hiring for a Remote Data Analyst to support our global healthcare data technology client. This individual will join a dedicated software development team supporting a clinical data platform used to derive insights across the clinical trial lifecycle. You will work closely with product owners and data engineers to validate data outputs, identify gaps, and support the development of meaningful, accurate insights from complex clinical datasets.This is a hands-on, judgment-intensive role ? you will be expected to move between defined analytical tasks and open-ended problem solving, often independently.Responsibilities Include: ? Validate data outputs and logic within the platform, identifying gaps, errors, and data loss across large enterprise datasets? Work with clinical data sources including CTMS platforms to assess data quality and completeness? Analyze competing analytical approaches and present reasoned recommendations on pros and cons? Support exploration phases by independently evaluating solutions and surfacing insights to the team? Communicate findings clearly in written reports, Excel, and PowerPointWe are a company committed to creating diverse and inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity/affirmative action employer that believes everyone matters. Qualified candidates will receive consideration for employment regardless of their race, color, ethnicity, religion, sex (including pregnancy), sexual orientation, gender identity and expression, marital status, national origin, ancestry, genetic factors, age, disability, protected veteran status, military or uniformed service member status, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or recruiting process, please send a request to HR@insightglobal.com.To learn more about how we collect, keep, and process your private information, please review Insight Global\u0027s Workforce Privacy Policy: https://insightglobal.com/workforce-privacy-policy/.","Title":"Data Analyst - INTL India","City":"New York","ExpirationDate":null,"PriorityOrder":0,"Requirements":"? 2-5 years of experience working with data in a Pharmaceutical, Biotech, or Clinical Research space/industry.? Hands on experience with any CTMS platform [Veeva Vault, Medidata Rave, Oracle Clinical One, Siebal, IQVIA, etc.]? Familiarity with external clinical datasets and clinical trial inclusion/exclusion criteria? Strong working knowledge of clinical trial terminology and data structures? Proficiency in SQL and Databricks","Skills":"? Python","Industry":"Data Warehousing","Country":"US","Division":"IGH","Office":null,"IsRemoteJob":true,"IsInternalJob":false,"ExtraValues":null,"__RecordIndex":0,"__OrdinalPosition":0,"__Timestamp":0,"Status":null,"ApplicantCount":0,"SubmittalCount":0,"ApplicationToHireRatio":0,"JobDuration":null,"SalaryHigh":12.0000,"SalaryLow":9.6000,"PayRateOvertime":0,"PayRateStraight":0,"Filled":0,"RemainingOpenings":0,"TotalOpenings":0,"Visa":null,"ClearanceType":null,"IsClearanceRequired":false,"IsHealthcare":false,"IsRemote":false,"EndClient":null,"JobCreatedDate":"\/Date(-62135578800000)\/","JobModifiedDate":"\/Date(-62135578800000)\/"}
Insight Global is hiring for a Remote Data Analyst to support our global healthcare data technology client. This individual will join a dedicated software development team supporting a clinical data... platform used to derive insights across the clinical trial lifecycle. You will work closely with product owners and data engineers to validate data outputs, identify gaps, and support the development of meaningful, accurate insights from complex clinical datasets.This is a hands-on, judgment-intensive role ? you will be expected to move between defined analytical tasks and open-ended problem solving, often independently.Responsibilities Include: ? Validate data outputs and logic within the platform, identifying gaps, errors, and data loss across large enterprise datasets? Work with clinical data sources including CTMS platforms to assess data quality and completeness? Analyze competing analytical approaches and present reasoned recommendations on pros and cons? Support exploration phases by independently evaluating solutions and surfacing insights to the team? Communicate findings clearly in written reports, Excel, and PowerPointWe are a company committed to creating diverse and inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity/affirmative action employer that believes everyone matters. Qualified candidates will receive consideration for employment regardless of their race, color, ethnicity, religion, sex (including pregnancy), sexual orientation, gender identity and expression, marital status, national origin, ancestry, genetic factors, age, disability, protected veteran status, military or uniformed service member status, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or recruiting process, please send a request to HR@insightglobal.com.To learn more about how we collect, keep, and process your private information, please review Insight Global's Workforce Privacy Policy: https://insightglobal.com/workforce-privacy-policy/.
Apr 10, 2026
Danvers, MA
|
Engineering (Non IT)
|
Contract
|
$16 - $20 (hourly estimate)
{"JobID":517365,"JobType":["Contract"],"EmployerID":null,"Location":{"Latitude":-70.9455,"Longitude":42.5694,"Distance":null},"State":"Massachusetts","Zip":"01923","ReferenceID":"BOS-cb7531cd-01e6-4799-a58c-986f39f88492","PostedDate":"\/Date(1775788653000)\/","Description":"Insight Global is seeking a Project Manager to support our Medical Device client. This consultant will sit remotely in Mexico and should have experience in a medical device environment, ideally supporting Quality Systems?related initiatives. This role will manage multiple, overlapping projects and work closely with senior stakeholders to drive execution and visibility. Day to day will consist of the following: Responsibilities-Manage multiple concurrent projects within a regulated medical device environment-Coordinate and communicate with senior-level stakeholders across teams-Develop and maintain project plans, timelines, and status updates-Prepare and coordinate slides, decks, and executive-ready presentations-Track risks, dependencies, and deliverables across initiativesCompensation: $16/hr to $20/hr. Exact compensation may vary based on several factors, including skills, experience, and educationWe are a company committed to creating diverse and inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity/affirmative action employer that believes everyone matters. Qualified candidates will receive consideration for employment regardless of their race, color, ethnicity, religion, sex (including pregnancy), sexual orientation, gender identity and expression, marital status, national origin, ancestry, genetic factors, age, disability, protected veteran status, military or uniformed service member status, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or recruiting process, please send a request to HR@insightglobal.com.To learn more about how we collect, keep, and process your private information, please review Insight Global\u0027s Workforce Privacy Policy: https://insightglobal.com/workforce-privacy-policy/.","Title":"Project Manager (INTL - Mexico)","City":"Danvers","ExpirationDate":null,"PriorityOrder":0,"Requirements":"-6-8+ years of project management experience within a medical device or regulated life sciences company-Exposure to Quality Systems initiatives or programs-Strong stakeholder management and communication skills-Ability to manage competing priorities in a fast-paced environment-Ability to manage training workflows and documentation in a regulated environment.-Excellent attention to detail, organizational skills, and ability to meet strict deadlines.-Proficiency in Microsoft Office Suite (Excel, Word, PowerPoint).-Experience with ComplianceWire is a plus, not required","Skills":"-Prior experience in medical device or pharmaceutical industry.-Familiarity with Windchill or other document management systems.-Experience supporting audit remediation projects (FDA, EU MDR, etc.).-Knowledge of Good Documentation Practices (GDP).","Industry":"Engineering (Non IT)","Country":"US","Division":"AF\u0026E","Office":null,"IsRemoteJob":true,"IsInternalJob":false,"ExtraValues":null,"__RecordIndex":0,"__OrdinalPosition":0,"__Timestamp":0,"Status":null,"ApplicantCount":0,"SubmittalCount":0,"ApplicationToHireRatio":0,"JobDuration":null,"SalaryHigh":20.0000,"SalaryLow":16.0000,"PayRateOvertime":0,"PayRateStraight":0,"Filled":0,"RemainingOpenings":0,"TotalOpenings":0,"Visa":null,"ClearanceType":null,"IsClearanceRequired":false,"IsHealthcare":false,"IsRemote":false,"EndClient":null,"JobCreatedDate":"\/Date(-62135578800000)\/","JobModifiedDate":"\/Date(-62135578800000)\/"}
Insight Global is seeking a Project Manager to support our Medical Device client. This consultant will sit remotely in Mexico and should have experience in a medical device environment, ideally... supporting Quality Systems?related initiatives. This role will manage multiple, overlapping projects and work closely with senior stakeholders to drive execution and visibility. Day to day will consist of the following: Responsibilities-Manage multiple concurrent projects within a regulated medical device environment-Coordinate and communicate with senior-level stakeholders across teams-Develop and maintain project plans, timelines, and status updates-Prepare and coordinate slides, decks, and executive-ready presentations-Track risks, dependencies, and deliverables across initiativesCompensation: $16/hr to $20/hr. Exact compensation may vary based on several factors, including skills, experience, and educationWe are a company committed to creating diverse and inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity/affirmative action employer that believes everyone matters. Qualified candidates will receive consideration for employment regardless of their race, color, ethnicity, religion, sex (including pregnancy), sexual orientation, gender identity and expression, marital status, national origin, ancestry, genetic factors, age, disability, protected veteran status, military or uniformed service member status, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or recruiting process, please send a request to HR@insightglobal.com.To learn more about how we collect, keep, and process your private information, please review Insight Global's Workforce Privacy Policy: https://insightglobal.com/workforce-privacy-policy/.
May 12, 2026
Wilmington, DE
|
QA
|
Contract
|
$34 - $42 (hourly estimate)
{"JobID":529372,"JobType":["Contract"],"EmployerID":null,"Location":{"Latitude":-75.53,"Longitude":39.73,"Distance":null},"State":"Delaware","Zip":"19803","ReferenceID":"KPD-479d2f82-26bf-4f1f-a987-1d83387aeeb8","PostedDate":"\/Date(1778597933000)\/","Description":"We are looking for an Technical Operations IT QA Consultant who will be responsible for functioning as a liaison between IT and Quality Assurance within Technical Operations. There will be both a project and support aspect to the role. Project related roles would be to serve as a subject matter and technical expert for the implementation of enhancements to Veeva QualitySuite Vaults (Quality Management, Document Management and Training). Support related roles would be to provide post go-live implementation and ongoing operational support for the end users and business administrators of the Veeva QualitySuite Vaults. This role will report to the IT Director of Technical Operations.Essential Functions of the Job:? Works with the Director, IT Tech Ops and QualitySuite System IT and Business Administrators to perform the above responsibilities.? Manages a team of offshore technical resources.? Prepares project related materials such as training guides, testing materials/scripts, support documents etc.? Addresses IT related issues beyond the core implementation based on knowledge of related IT areas. ? Ensures the smooth and timely implementation of new configuration, reports, and additional phase/releases to existing applications. ? Ability to work both independently and within a team structure and be proactive in recommending and implementing solutions. ? Performs/assists with configuration application testing, quality assurance, computer system validation, implementation, and support.? Serves as the subject matter and technical expert for the implementation of Projects and Enhancements to Veeva QualitySuite.? Partners with the Business system owners/Business Administrators to implement systems that support their requirements/business processes meeting delivery targets.? Understands the business processes and technical workflows.? Provides functional and technical support for the Veeva QualitySuite Tech Ops business administrators and users both in US and Europe.We are a company committed to creating diverse and inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity/affirmative action employer that believes everyone matters. Qualified candidates will receive consideration for employment regardless of their race, color, ethnicity, religion, sex (including pregnancy), sexual orientation, gender identity and expression, marital status, national origin, ancestry, genetic factors, age, disability, protected veteran status, military or uniformed service member status, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or recruiting process, please send a request to HR@insightglobal.com.To learn more about how we collect, keep, and process your private information, please review Insight Global\u0027s Workforce Privacy Policy: https://insightglobal.com/workforce-privacy-policy/.","Title":"Veeva Quality IT QA","City":"Wilmington","ExpirationDate":null,"PriorityOrder":0,"Requirements":"? Experience with project delivery, good presentation skills, and leadership in a team environment.? Ability to work independently and manage multiple tasks with changing priorities.? Strong interpersonal and communication skills.? Veeva Vault support experience required with Configuration and QualitySuite experience? Five plus years of pharmaceutical/life sciences experience.? Bachelor?s degree or equivalent.? Working knowledge of FDA compliance, computer systems validation, 21CFR Part 11 regulations and GAMP guideline","Skills":"? Veeva System Administration certification preferred as a Certified Veeva Quality Associate and Certified Vault Platform Administrator.","Industry":"QA","Country":"US","Division":"IT","Office":null,"IsRemoteJob":true,"IsInternalJob":false,"ExtraValues":null,"__RecordIndex":0,"__OrdinalPosition":0,"__Timestamp":0,"Status":null,"ApplicantCount":0,"SubmittalCount":0,"ApplicationToHireRatio":0,"JobDuration":null,"SalaryHigh":42.0000,"SalaryLow":33.6000,"PayRateOvertime":0,"PayRateStraight":0,"Filled":0,"RemainingOpenings":0,"TotalOpenings":0,"Visa":null,"ClearanceType":null,"IsClearanceRequired":false,"IsHealthcare":false,"IsRemote":false,"EndClient":null,"JobCreatedDate":"\/Date(-62135578800000)\/","JobModifiedDate":"\/Date(-62135578800000)\/"}
We are looking for an Technical Operations IT QA Consultant who will be responsible for functioning as a liaison between IT and Quality Assurance within Technical Operations. There will be both a... project and support aspect to the role. Project related roles would be to serve as a subject matter and technical expert for the implementation of enhancements to Veeva QualitySuite Vaults (Quality Management, Document Management and Training). Support related roles would be to provide post go-live implementation and ongoing operational support for the end users and business administrators of the Veeva QualitySuite Vaults. This role will report to the IT Director of Technical Operations.Essential Functions of the Job:? Works with the Director, IT Tech Ops and QualitySuite System IT and Business Administrators to perform the above responsibilities.? Manages a team of offshore technical resources.? Prepares project related materials such as training guides, testing materials/scripts, support documents etc.? Addresses IT related issues beyond the core implementation based on knowledge of related IT areas. ? Ensures the smooth and timely implementation of new configuration, reports, and additional phase/releases to existing applications. ? Ability to work both independently and within a team structure and be proactive in recommending and implementing solutions. ? Performs/assists with configuration application testing, quality assurance, computer system validation, implementation, and support.? Serves as the subject matter and technical expert for the implementation of Projects and Enhancements to Veeva QualitySuite.? Partners with the Business system owners/Business Administrators to implement systems that support their requirements/business processes meeting delivery targets.? Understands the business processes and technical workflows.? Provides functional and technical support for the Veeva QualitySuite Tech Ops business administrators and users both in US and Europe.We are a company committed to creating diverse and inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity/affirmative action employer that believes everyone matters. Qualified candidates will receive consideration for employment regardless of their race, color, ethnicity, religion, sex (including pregnancy), sexual orientation, gender identity and expression, marital status, national origin, ancestry, genetic factors, age, disability, protected veteran status, military or uniformed service member status, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or recruiting process, please send a request to HR@insightglobal.com.To learn more about how we collect, keep, and process your private information, please review Insight Global's Workforce Privacy Policy: https://insightglobal.com/workforce-privacy-policy/.
Apr 24, 2026
Danvers, MA
|
Engineering (Non IT)
|
Contract
|
$16 - $20 (hourly estimate)
{"JobID":523082,"JobType":["Contract"],"EmployerID":null,"Location":{"Latitude":-70.9455,"Longitude":42.5694,"Distance":null},"State":"Massachusetts","Zip":"01923","ReferenceID":"BOS-d2df46a4-0294-45ba-89c4-5029230fd2e8","PostedDate":"\/Date(1777057449000)\/","Description":"Insight Global is seeking a Project Manager to support our Medical Device client. This consultant will sit remotely in Mexico and should have experience in a medical device environment, ideally supporting Quality Systems?related initiatives. This role will manage multiple, overlapping projects and work closely with senior stakeholders to drive execution and visibility. Day to day will consist of the following: Responsibilities-Assist with creating training packages for internal enterprise customers, specifically centered around ComplianceWire and additional LMS system-Manage multiple concurrent projects within a regulated medical device environment-Coordinate and communicate with senior-level stakeholders across teams-Develop and maintain project plans, timelines, and status updates-Prepare and coordinate slides, decks, and executive-ready presentations-Track risks, dependencies, and deliverables across initiativesCompensation: $16/hr to $20/hr. Exact compensation may vary based on several factors, including skills, experience, and educationWe are a company committed to creating diverse and inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity/affirmative action employer that believes everyone matters. Qualified candidates will receive consideration for employment regardless of their race, color, ethnicity, religion, sex (including pregnancy), sexual orientation, gender identity and expression, marital status, national origin, ancestry, genetic factors, age, disability, protected veteran status, military or uniformed service member status, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or recruiting process, please send a request to HR@insightglobal.com.To learn more about how we collect, keep, and process your private information, please review Insight Global\u0027s Workforce Privacy Policy: https://insightglobal.com/workforce-privacy-policy/.","Title":"Project Manager - LMS (INTL - Mexico)","City":"Danvers","ExpirationDate":null,"PriorityOrder":0,"Requirements":"-6-8+ years of project management experience within a medical device or regulated life sciences company-Exposure to Quality Systems initiatives or programs-Strong stakeholder management and communication skills-Ability to manage competing priorities in a fast-paced environment-Ability to manage training workflows and documentation in a regulated environment.-Excellent attention to detail, organizational skills, and ability to meet strict deadlines.-Proficiency in Microsoft Office Suite (Excel, Word, PowerPoint).-Experience with ComplianceWire or relative LMS systems","Skills":"-Prior experience in medical device or pharmaceutical industry.-Familiarity with Windchill or other document management systems.-Experience supporting audit remediation projects (FDA, EU MDR, etc.).-Knowledge of Good Documentation Practices (GDP).","Industry":"Engineering (Non IT)","Country":"US","Division":"AF\u0026E","Office":null,"IsRemoteJob":true,"IsInternalJob":false,"ExtraValues":null,"__RecordIndex":0,"__OrdinalPosition":0,"__Timestamp":0,"Status":null,"ApplicantCount":0,"SubmittalCount":0,"ApplicationToHireRatio":0,"JobDuration":null,"SalaryHigh":20.0000,"SalaryLow":16.0000,"PayRateOvertime":0,"PayRateStraight":0,"Filled":0,"RemainingOpenings":0,"TotalOpenings":0,"Visa":null,"ClearanceType":null,"IsClearanceRequired":false,"IsHealthcare":false,"IsRemote":false,"EndClient":null,"JobCreatedDate":"\/Date(-62135578800000)\/","JobModifiedDate":"\/Date(-62135578800000)\/"}
Insight Global is seeking a Project Manager to support our Medical Device client. This consultant will sit remotely in Mexico and should have experience in a medical device environment, ideally... supporting Quality Systems?related initiatives. This role will manage multiple, overlapping projects and work closely with senior stakeholders to drive execution and visibility. Day to day will consist of the following: Responsibilities-Assist with creating training packages for internal enterprise customers, specifically centered around ComplianceWire and additional LMS system-Manage multiple concurrent projects within a regulated medical device environment-Coordinate and communicate with senior-level stakeholders across teams-Develop and maintain project plans, timelines, and status updates-Prepare and coordinate slides, decks, and executive-ready presentations-Track risks, dependencies, and deliverables across initiativesCompensation: $16/hr to $20/hr. Exact compensation may vary based on several factors, including skills, experience, and educationWe are a company committed to creating diverse and inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity/affirmative action employer that believes everyone matters. Qualified candidates will receive consideration for employment regardless of their race, color, ethnicity, religion, sex (including pregnancy), sexual orientation, gender identity and expression, marital status, national origin, ancestry, genetic factors, age, disability, protected veteran status, military or uniformed service member status, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or recruiting process, please send a request to HR@insightglobal.com.To learn more about how we collect, keep, and process your private information, please review Insight Global's Workforce Privacy Policy: https://insightglobal.com/workforce-privacy-policy/.
May 08, 2026
Santa Barbara, CA
|
Architect (Engineering)
|
Perm
|
$160k - $240k (estimate)
{"JobID":528133,"JobType":["Perm"],"EmployerID":null,"Location":{"Latitude":-119.7,"Longitude":34.41,"Distance":null},"State":"California","Zip":"93101","ReferenceID":"DGW-f7830f6a-09ad-4d60-a0f8-74627005d7d9","PostedDate":"\/Date(1778202130000)\/","Description":"A leading consulting organization is seeking a hands-on, GCP-certified AI Architect to design and deliver production-grade agentic pipelines built on Vertex AI. This role operates as a core delivery resource embedded within active engagements, partnering directly with cloud platform teams and client stakeholders. This is a hands-on delivery role (not advisory). The Architect will contribute at the code, architecture, and implementation level from day one and is accountable for delivering production-ready pipelines, agent frameworks, integrations, and security controls.We are a company committed to creating diverse and inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity/affirmative action employer that believes everyone matters. Qualified candidates will receive consideration for employment regardless of their race, color, ethnicity, religion, sex (including pregnancy), sexual orientation, gender identity and expression, marital status, national origin, ancestry, genetic factors, age, disability, protected veteran status, military or uniformed service member status, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or recruiting process, please send a request to HR@insightglobal.com.To learn more about how we collect, keep, and process your private information, please review Insight Global\u0027s Workforce Privacy Policy: https://insightglobal.com/workforce-privacy-policy/.","Title":"Senior AI Solutions Engineer","City":"Santa Barbara","ExpirationDate":null,"PriorityOrder":0,"Requirements":"?Active Google Cloud Professional certification (Architect, Data Engineer, or ML Engineer); current, not lapsed ?Production Vertex AI agentic pipeline experience; built and shipped at scale, not demos ?GCP data pipeline engineering experience with Dataflow, Beam, Airflow, and BigQuery in production environments ?FHIR Server API integration experience (R4 minimum) built against a real server ?Pipeline observability experience including failure handling, retry logic, metrics, and drift detection ?Current possession of 4 out of 5 Gemini Enterprise for Customer Experience (GECX) technical skill badges ?GCP security model design experience including IAM, service account governance, agent identity, and log retention in regulated environments ?Active Google Cloud Delivery Readiness Program (DRP) Tier 1 score (50+) in a relevant product/solution area (e.g., Vertex AI / Generative AI).","Skills":"?Life sciences, pharmaceutical, or GxP environment experience ?Google Professional Services or large global systems integrator GCP practice background ?FHIR R5 depth sufficient to hold design conversations with FHIR engineers ?Familiarity with large-scale enterprise data environments","Industry":"Architect (Engineering)","Country":"US","Division":"IT","Office":null,"IsRemoteJob":true,"IsInternalJob":false,"ExtraValues":null,"__RecordIndex":0,"__OrdinalPosition":0,"__Timestamp":0,"Status":null,"ApplicantCount":0,"SubmittalCount":0,"ApplicationToHireRatio":0,"JobDuration":null,"SalaryHigh":240000.0000,"SalaryLow":160000.0000,"PayRateOvertime":0,"PayRateStraight":0,"Filled":0,"RemainingOpenings":0,"TotalOpenings":0,"Visa":null,"ClearanceType":null,"IsClearanceRequired":false,"IsHealthcare":false,"IsRemote":false,"EndClient":null,"JobCreatedDate":"\/Date(-62135578800000)\/","JobModifiedDate":"\/Date(-62135578800000)\/"}
A leading consulting organization is seeking a hands-on, GCP-certified AI Architect to design and deliver production-grade agentic pipelines built on Vertex AI. This role operates as a core delivery... resource embedded within active engagements, partnering directly with cloud platform teams and client stakeholders. This is a hands-on delivery role (not advisory). The Architect will contribute at the code, architecture, and implementation level from day one and is accountable for delivering production-ready pipelines, agent frameworks, integrations, and security controls.We are a company committed to creating diverse and inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity/affirmative action employer that believes everyone matters. Qualified candidates will receive consideration for employment regardless of their race, color, ethnicity, religion, sex (including pregnancy), sexual orientation, gender identity and expression, marital status, national origin, ancestry, genetic factors, age, disability, protected veteran status, military or uniformed service member status, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or recruiting process, please send a request to HR@insightglobal.com.To learn more about how we collect, keep, and process your private information, please review Insight Global's Workforce Privacy Policy: https://insightglobal.com/workforce-privacy-policy/.