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Feb 18, 2026

Pittsburgh, PA

|

Laboratory Technician

|

Perm

|

$55k - $60k (estimate)

{"JobID":496401,"JobType":["Perm"],"EmployerID":null,"Location":{"Latitude":-79.97,"Longitude":40.43,"Distance":null},"State":"Pennsylvania","Zip":"15213","ReferenceID":"PIT-3ca4b9d2-47aa-4114-b7af-1c722d82e0e5","PostedDate":"\/Date(1771440560000)\/","Description":"The Demetris Research Histology Services (RHS) laboratory provides complete translational research histology services which include serving as a core lab for the Immune Tolerance Network (ITN), multiple Clinical Trials in Organ Transplantation (CTOT), and multiple grants and corporate local, national, and international clinical trials. The RHS lab specializes in sample preparation, sectioning, routine staining, and immunohistochemistry services. Currently, we are providing these services for twelve sponsors with additional contracts pending. Possible need for another lab technician to assist with the workflow and allow the lab to meet project requirements. Manages day-to-day laboratory operations while ensuring compliance with safety regulations and best practices. Works with, adapts, and installs scientific equipment in research laboratories. Develops and collaborates on routine projects and procedures. Manages inventory and equipment and performs budget functions. Essential Functions:?Must be able to perform all basic histology and immunohistochemistry procedures: grossing, processing, embedding, sectioning, special stains, equipment maintenance, other routine lab tasks?Follow established protocols and troubleshoot basic immunohistochemistry as necessary?Compliance with regulatory training and EHS requirements?Will be handling the entire lifecycleWe 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":"Histology Technologist","City":"Pittsburgh","ExpirationDate":null,"PriorityOrder":0,"Requirements":"?Bachelors or Associates DegreeoCombination of education and relevant experience will be considered in lieu of education and/ or experience requirement.?At least a year of experience in a wet lab as a histotechnologist ?Ability to work independently with little supervision","Skills":"?Histotechnician Certification (HT ASCP) or Histotechnologist Certification? Managerial Experience","Industry":"Laboratory Technician","Country":"US","Division":"IT","Office":null,"IsRemoteJob":false,"IsInternalJob":false,"ExtraValues":null,"__RecordIndex":0,"__OrdinalPosition":0,"__Timestamp":0,"Status":null,"ApplicantCount":0,"SubmittalCount":0,"ApplicationToHireRatio":0,"JobDuration":null,"SalaryHigh":60000.0000,"SalaryLow":55000.0000,"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)\/"}

The Demetris Research Histology Services (RHS) laboratory provides complete translational research histology services which include serving as a core lab for the Immune Tolerance Network (ITN),... multiple Clinical Trials in Organ Transplantation (CTOT), and multiple grants and corporate local, national, and international clinical trials. The RHS lab specializes in sample preparation, sectioning, routine staining, and immunohistochemistry services. Currently, we are providing these services for twelve sponsors with additional contracts pending. Possible need for another lab technician to assist with the workflow and allow the lab to meet project requirements. Manages day-to-day laboratory operations while ensuring compliance with safety regulations and best practices. Works with, adapts, and installs scientific equipment in research laboratories. Develops and collaborates on routine projects and procedures. Manages inventory and equipment and performs budget functions. Essential Functions:?Must be able to perform all basic histology and immunohistochemistry procedures: grossing, processing, embedding, sectioning, special stains, equipment maintenance, other routine lab tasks?Follow established protocols and troubleshoot basic immunohistochemistry as necessary?Compliance with regulatory training and EHS requirements?Will be handling the entire lifecycleWe 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 20, 2026

Hackensack, NJ

|

Nurse

|

Perm

|

$110k - $120k (estimate)

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Insight Global is seeking a Clinical Research Nurse (Transplant) to support the transplant oncology program at Hackensack Meridian Health in Hackensack, NJ. This role prioritizes direct patient care,... with responsibilities flexing based on daily clinic volume?larger patient schedules require more patient-facing time. The nurse balances clinical care and research coordination, typically seeing 3?5 study patients per day, and is responsible for screening patients for protocol eligibility, presenting studies and obtaining informed consent, conducting study-specific assessments, managing nursing and chemotherapy orders in collaboration with oncology and pharmacy teams, triaging patient phone calls, and ensuring patient schedules remain accurate and up to date. Additional responsibilities include attending study teleconferences, addressing data queries and source documentation, and partnering with data coordinators and the regulatory team to ensure nursing-focused compliance with IRB, sponsor, and institutional requirements in a fast-paced oncology environment.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 27, 2026

Jupiter, FL

|

EMR ? Electronic Medical Records

|

Perm

|

$77k - $100k (estimate)

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Jupiter Medical Center is seeking a Unified Communications Engineer to design, deploy, and support enterprise communication and collaboration solutions across a campus-based and remote healthcare... environment. This role is responsible for maintaining highly available voice, video, messaging, conferencing, and mobility solutions that support clinical and business operations.This is a hands-on engineering role, not project management. The engineer will lead Tier-3 troubleshooting, support incident and disaster response communications, and partner closely with clinical teams, IT leadership, and vendors to improve communication reliability and user experience. The role also contributes to enterprise mobility strategy, conference room solutions, and ongoing optimization of unified communications platforms.This position is ideal for a senior-level UC engineer with healthcare experience who enjoys owning complex systems, mentoring others, and supporting mission-critical communications in a hospital environment.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 03, 2026

Groton, CT

|

Warehouse

|

Contract,Perm Possible

|

$29 - $36 (hourly estimate)

{"JobID":501754,"JobType":["Contract,Perm Possible"],"EmployerID":null,"Location":{"Latitude":-72.0368,"Longitude":41.3534,"Distance":null},"State":"Connecticut","Zip":"06340","ReferenceID":"HNJ-c5cb5ce0-265a-471a-9f6d-44e35b971667","PostedDate":"\/Date(1772553718000)\/","Description":"2 years of relevant experience or in a similar environmentExcellent documentation, computer literacy in MS word Perform primary and secondary GMP packaging operations in strict accordance with approved batch records, cGMPs, SOPs, and safety regulations Accurately complete all required GMP documentation to ensure contemporaneous and compliant records of equipment use and packaging activities Handle, move, and package clinical trial materials while fully adhering to safety, quality, and regulatory requirements Use the approved inventory system (CAIS) to scan materials and execute packaging-related tasks Support routine daily, weekly, monthly, and quarterly cleaning and maintenance of GMP packaging rooms and equipment Follow production schedules and timelines while assisting with resolution of common equipment or process issues Comply with all gowning, hygiene, and cleanroom requirements, including restrictions on makeup, jewelry, and personal items Meet physical and cognitive demands of the role, including prolonged standing, lifting up to 45 lbs, and sustained mental, visual, and manual attentionWe 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":"Packaging Technician","City":"Groton","ExpirationDate":null,"PriorityOrder":0,"Requirements":"A client of Insight Global is looking to onboard several Packaging and Labeling Technicians in Groton, CT. The Packaging and Labelling Technician role must maintain daily compliance to Standard Operating Procedures (SOPs), in accordance with current Good Manufacturing Practice (cGMP) guidelines and is responsible for performing operations to support the packaging and labelling of clinical trial supplies. The Technician role performs both Primary Packaging and Secondary Packaging Operations. This may include (but is not limited to): solid dose drug product by way of manual hand count filling into bottles or by use of minor equipment for automated filling, packaging finished dosage forms such as filled bottles, ointments, pre-filled vials and labelling of other pre-packaged finished material. This position is also responsible to maintain the packaging equipment for daily use including cleaning.","Skills":"","Industry":"Warehouse","Country":"US","Division":"IGH","Office":null,"IsRemoteJob":false,"IsInternalJob":false,"ExtraValues":null,"__RecordIndex":0,"__OrdinalPosition":0,"__Timestamp":0,"Status":null,"ApplicantCount":0,"SubmittalCount":0,"ApplicationToHireRatio":0,"JobDuration":null,"SalaryHigh":36.0000,"SalaryLow":28.8000,"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)\/"}

2 years of relevant experience or in a similar environmentExcellent documentation, computer literacy in MS word Perform primary and secondary GMP packaging operations in strict accordance with... approved batch records, cGMPs, SOPs, and safety regulations Accurately complete all required GMP documentation to ensure contemporaneous and compliant records of equipment use and packaging activities Handle, move, and package clinical trial materials while fully adhering to safety, quality, and regulatory requirements Use the approved inventory system (CAIS) to scan materials and execute packaging-related tasks Support routine daily, weekly, monthly, and quarterly cleaning and maintenance of GMP packaging rooms and equipment Follow production schedules and timelines while assisting with resolution of common equipment or process issues Comply with all gowning, hygiene, and cleanroom requirements, including restrictions on makeup, jewelry, and personal items Meet physical and cognitive demands of the role, including prolonged standing, lifting up to 45 lbs, and sustained mental, visual, and manual attentionWe 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/.

Dec 10, 2025

Midlothian, VA

|

Audit

|

Perm

|

$100k - $110k (estimate)

{"JobID":475197,"JobType":["Perm"],"EmployerID":null,"Location":{"Latitude":-77.46,"Longitude":37.55,"Distance":null},"State":"Virginia","Zip":"23235","ReferenceID":"RIC-d6cc30ef-d3d5-4614-af1c-38f8993a91e7","PostedDate":"\/Date(1765404821000)\/","Description":"Insight Global is looking for a GDMP Auditor to support a Pharmaceutical company in Richmond, VA. The GMDP/GCP Auditor is responsible for planning, conducting and reporting audits related to Good Manufacturing and Distribution Practices (GMDP) and Good Clinical Practices (GCP) ensuring compliance with global regulatory standards and company policies. This ensures that pharmaceutical, biotechnology, and clinical pharmaceutical, adhere to applicable guidelines, maintaining product quality, patient safety, and data integrity.Salary range: $100,000-$110,000We 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":"GMDP Auditor","City":"Midlothian","ExpirationDate":null,"PriorityOrder":0,"Requirements":"- Minimum 5 recent years external auditing experience in a regulated environment such as pharmaceuticals- Proven ability to manage audit programs, supplier qualifications, vendor agreements, and CAPAs","Skills":"","Industry":"Audit","Country":"US","Division":"AF\u0026E","Office":null,"IsRemoteJob":false,"IsInternalJob":false,"ExtraValues":null,"__RecordIndex":0,"__OrdinalPosition":0,"__Timestamp":0,"Status":null,"ApplicantCount":0,"SubmittalCount":0,"ApplicationToHireRatio":0,"JobDuration":null,"SalaryHigh":110000.0000,"SalaryLow":100000.0000,"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 looking for a GDMP Auditor to support a Pharmaceutical company in Richmond, VA. The GMDP/GCP Auditor is responsible for planning, conducting and reporting audits related to Good... Manufacturing and Distribution Practices (GMDP) and Good Clinical Practices (GCP) ensuring compliance with global regulatory standards and company policies. This ensures that pharmaceutical, biotechnology, and clinical pharmaceutical, adhere to applicable guidelines, maintaining product quality, patient safety, and data integrity.Salary range: $100,000-$110,000We 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/.

Oct 28, 2025

Kentwood, MI

|

Medical Assistant

|

Contract-to-perm

|

$17 - $21 (hourly estimate)

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Insight global is seeking a Certified Medical Assistant (CMA) This role involves both front and back office duties, including performing blood draws, EKGs, and pulmonary function tests (PFTs), as... well as handling administrative tasks such as scheduling, patient intake, and managing medical records. The ideal candidate will be comfortable working in a fast-paced clinical environment, supporting providers during exams, and ensuring smooth day-to-day operations across both clinical and administrative functions..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/.

Oct 14, 2025

Saint-Paul, MN

|

Biomedical Engineering

|

Contract

|

$36 - $45 (hourly estimate)

{"JobID":455421,"JobType":["Contract"],"EmployerID":null,"Location":{"Latitude":-93.1,"Longitude":44.94,"Distance":null},"State":"Minnesota","Zip":"55101","ReferenceID":"HNC-f18df179-b2c2-4118-8140-16afa3d28161","PostedDate":"\/Date(1760477122000)\/","Description":"The Medical Equipment Repair Technician is responsible for the servicing and preventative maintenance, electrical safety inspections, performance verification, and repairs on highly technical clinical equipment, documentation of all work performed, and to participate in safety and quality improvement programs.Other responsibilities include:Evaluates malfunctioning equipment, troubleshoots, calibrates and repairs electronic equipment.Perform scheduled safety testing and preventive maintenance.Provides Clinical SupportIssues purchase orders and requisitions for parts, supplies and equipmentWe 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":"Biomedical Equipment Technician","City":"Saint-Paul","ExpirationDate":null,"PriorityOrder":0,"Requirements":"Strong hardware repair experience with Biomedical Electronics, hands-on working with tools to repair broken hospital/medical equipment- can take apart, test, and fix devices such as but not limited to: patient monitors, suction regulators, infusion pipes *Experience may be from military, home health, hospital, OEM (original equipment manufacturer), or retail company that sells refurbished medical equipment (example: medical equipment or medical equipment repair company like Agiliti, USOC Medical, Probo Medical, Sodexo USA, Trimedx where on a bench)","Skills":"Two-year degree in Medical Equipment TechnologyCertification as a Certified Biomedical Equipment Technician through the Association for the Advancement of Medical Instrumentation (AAMI)","Industry":"Biomedical Engineering","Country":"US","Division":"IGH","Office":null,"IsRemoteJob":false,"IsInternalJob":false,"ExtraValues":null,"__RecordIndex":0,"__OrdinalPosition":0,"__Timestamp":0,"Status":null,"ApplicantCount":0,"SubmittalCount":0,"ApplicationToHireRatio":0,"JobDuration":null,"SalaryHigh":45.0000,"SalaryLow":36.0000,"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)\/"}

The Medical Equipment Repair Technician is responsible for the servicing and preventative maintenance, electrical safety inspections, performance verification, and repairs on highly technical... clinical equipment, documentation of all work performed, and to participate in safety and quality improvement programs.Other responsibilities include:Evaluates malfunctioning equipment, troubleshoots, calibrates and repairs electronic equipment.Perform scheduled safety testing and preventive maintenance.Provides Clinical SupportIssues purchase orders and requisitions for parts, supplies and equipmentWe 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/.

Aug 27, 2024

Austin, TX

|

Computer Engineering

|

Contract

|

$56 - $70 (hourly estimate)

{"JobID":377203,"JobType":["Contract"],"EmployerID":null,"Location":{"Latitude":-97.7277272727273,"Longitude":30.2664545454545,"Distance":null},"State":"Texas","Zip":"78752","ReferenceID":"HSW-dca3d5d7-1ec0-42a6-b6d3-e3bd761b8d4f","PostedDate":"\/Date(1724775441000)\/","Description":"Job Description:We are seeking a Senior Backend Engineer to join our Clinical Transformation Workflow team. This role involves working on high-priority projects related to CMS regulatory requirements, including hip and knee surgery scheduling and post-surgery follow-ups. The engineer will primarily focus on developing backend APIs for our front-end applications, ensuring seamless integration with various EHR systems like Athena, Cerner, Epic, Allscripts, and Meditech.Key Responsibilities: *Develop and maintain backend APIs for clinical transformation projects. *Work on CMS regulatory requirement projects, including hip and knee surgery scheduling. *Integrate backend services with EHR systems (Athena, Cerner, Epic, Allscripts, Meditech). *Collaborate with front-end developers to ensure seamless integration. *Maintain a minimum of 80% code coverage for all implementations. *Participate in daily stand-up calls and scrum ceremonies.We are a company committed to creating inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity employer that believes everyone matters. Qualified candidates will receive consideration for employment opportunities without regard to race, religion, sex, age, marital status, national origin, sexual orientation, citizenship status, disability, 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 Human Resources Request Form. The EEOC \"Know Your Rights\" Poster is available here. 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":"Sr Java Developer","City":"Austin","ExpirationDate":null,"PriorityOrder":0,"Requirements":"REQUIRED SKILLS AND EXPERIENCETop Skills:12 years of JavaW2 only *Proficiency in Java and Spring Boot. *Experience with healthcare-based requests and Smart on FHIR apps. *Knowledge of HL7 standards. *Strong understanding of backend API development and integration. *Familiarity with EHR systems (Athena, Cerner, Epic, Allscripts, Meditech).","Skills":"","Industry":"Computer Engineering","Country":"US","Division":"IT","Office":null,"IsRemoteJob":false,"IsInternalJob":false,"ExtraValues":null,"__RecordIndex":0,"__OrdinalPosition":0,"__Timestamp":0,"Status":null,"ApplicantCount":0,"SubmittalCount":0,"ApplicationToHireRatio":0,"JobDuration":null,"SalaryHigh":70.0000,"SalaryLow":56.0000,"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)\/"}

Job Description:We are seeking a Senior Backend Engineer to join our Clinical Transformation Workflow team. This role involves working on high-priority projects related to CMS regulatory... requirements, including hip and knee surgery scheduling and post-surgery follow-ups. The engineer will primarily focus on developing backend APIs for our front-end applications, ensuring seamless integration with various EHR systems like Athena, Cerner, Epic, Allscripts, and Meditech.Key Responsibilities: *Develop and maintain backend APIs for clinical transformation projects. *Work on CMS regulatory requirement projects, including hip and knee surgery scheduling. *Integrate backend services with EHR systems (Athena, Cerner, Epic, Allscripts, Meditech). *Collaborate with front-end developers to ensure seamless integration. *Maintain a minimum of 80% code coverage for all implementations. *Participate in daily stand-up calls and scrum ceremonies.We are a company committed to creating inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity employer that believes everyone matters. Qualified candidates will receive consideration for employment opportunities without regard to race, religion, sex, age, marital status, national origin, sexual orientation, citizenship status, disability, 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 Human Resources Request Form. The EEOC "Know Your Rights" Poster is available here. 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 03, 2026

Rahway, NJ

|

Mechanical Engineering

|

Contract-to-perm

|

$54 - $68 (hourly estimate)

{"JobID":490136,"JobType":["Contract-to-perm"],"EmployerID":null,"Location":{"Latitude":-74.2824,"Longitude":40.6077,"Distance":null},"State":"New Jersey","Zip":"07065","ReferenceID":"NNJ-72edbe36-58b6-447c-bbe2-601ea7f17f0a","PostedDate":"\/Date(1770143945000)\/","Description":"The Design Verification Consultant will be responsible for shaping and executing design verification approaches for drug-device and combination product development programs. This role supports testing readiness and execution across component, subassembly, and finished product levels, including activities tied to clinical and commercialization pathways.Working closely with cross-functional stakeholders and external testing partners, the consultant will provide technical leadership across verification planning, method development, and testing execution. The position also contributes to adjacent activities such as manufacturing process validation, stability programs, and final assembly readiness. Success in this role requires strong technical judgment, proactive problem solving, and the ability to influence and align diverse teams.Key ResponsibilitiesDefine and drive design verification strategies supporting drug-device and combination product development programs across clinical and commercial phases.Develop, author, and execute design verification plans, protocols, and reports demonstrating alignment between product requirements and verification outcomes.Establish and guide development, qualification, and validation of test methods in alignment with applicable standards and regulatory expectations.Lead verification execution across internal teams and external laboratories, ensuring timelines, quality, and technical rigor are maintained.Plan and manage accelerated and real-time aging studies, including bridging approaches at component, subassembly, and finished product levels.Support testing readiness for critical development and commercialization activities such as Stability studies. Drug, product filling validations, Final assembly process validations, Transportation and distribution testing.Partner with quality, engineering, manufacturing, and regulatory functions to establish incoming inspection and release testing strategies.Provide oversight and technical direction to third-party testing vendors and development partners.Identify risks and constraints early, propose mitigation strategies, and communicate progress, challenges, and technical decisions to stakeholders.Support clinical supply builds by ensuring verification activities align with testing and release requirements.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":"Design Verification Consultant ? Combination Products","City":"Rahway","ExpirationDate":null,"PriorityOrder":0,"Requirements":"8+ years of combination product development experience focused on design verification (Auto-injector, ophthalmic, and DPI)Experience supporting or leading design verification for combination product programs, including development of verification strategies, plans, protocols, reports, and associated test method developmentExperience with design controls, risk management practices, material selection and molding processes, manufacturing process development and validation, secondary packaging qualification, and overall design validationKnowledge performance testing related to container closure integrity (CCI), dose accuracy, and functional performanceKnowledge of industry standards related to ISO 11608, ISO 11040, and ISO 80369","Skills":"Experience in SolidWorksAdvanced Degree in a related field","Industry":"Mechanical Engineering","Country":"US","Division":"AF\u0026E","Office":null,"IsRemoteJob":false,"IsInternalJob":false,"ExtraValues":null,"__RecordIndex":0,"__OrdinalPosition":0,"__Timestamp":0,"Status":null,"ApplicantCount":0,"SubmittalCount":0,"ApplicationToHireRatio":0,"JobDuration":null,"SalaryHigh":68.0000,"SalaryLow":54.4000,"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 Design Verification Consultant will be responsible for shaping and executing design verification approaches for drug-device and combination product development programs. This role supports... testing readiness and execution across component, subassembly, and finished product levels, including activities tied to clinical and commercialization pathways.Working closely with cross-functional stakeholders and external testing partners, the consultant will provide technical leadership across verification planning, method development, and testing execution. The position also contributes to adjacent activities such as manufacturing process validation, stability programs, and final assembly readiness. Success in this role requires strong technical judgment, proactive problem solving, and the ability to influence and align diverse teams.Key ResponsibilitiesDefine and drive design verification strategies supporting drug-device and combination product development programs across clinical and commercial phases.Develop, author, and execute design verification plans, protocols, and reports demonstrating alignment between product requirements and verification outcomes.Establish and guide development, qualification, and validation of test methods in alignment with applicable standards and regulatory expectations.Lead verification execution across internal teams and external laboratories, ensuring timelines, quality, and technical rigor are maintained.Plan and manage accelerated and real-time aging studies, including bridging approaches at component, subassembly, and finished product levels.Support testing readiness for critical development and commercialization activities such as Stability studies. Drug, product filling validations, Final assembly process validations, Transportation and distribution testing.Partner with quality, engineering, manufacturing, and regulatory functions to establish incoming inspection and release testing strategies.Provide oversight and technical direction to third-party testing vendors and development partners.Identify risks and constraints early, propose mitigation strategies, and communicate progress, challenges, and technical decisions to stakeholders.Support clinical supply builds by ensuring verification activities align with testing and release requirements.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 02, 2026

Warwick, RI

|

Nurse

|

Contract,Perm Possible

|

$27 - $34 (hourly estimate)

{"JobID":501038,"JobType":["Contract,Perm Possible"],"EmployerID":null,"Location":{"Latitude":-71.4442,"Longitude":41.7027,"Distance":null},"State":"Rhode Island","Zip":"02886","ReferenceID":"DGH-bc3e9f88-740b-470c-b03a-fd4c78e751f2","PostedDate":"\/Date(1772463382000)\/","Description":"The Hospice LPN plans, coordinates, and delivers compassionate end-of-life care to patients and families within their homes and community settings. This role performs comprehensive assessments, develops and manages individualized plans of care, and provides skilled nursing services focused on comfort, symptom management, and quality of life. The LPN serves as a key member of the interdisciplinary hospice team, acting as a patient advocate and clinical resource. As assigned, the nurse functions as a Case Manager, coordinating services and supervising hospice aides to ensure continuity of care. The position requires strong clinical judgment, communication skills, and the ability to work with a team in a facility and in-home setting.Key ResponsibilitiesPerform initial, ongoing, and comprehensive assessments of patients and families to determine hospice needsDevelop, implement, and regularly revise individualized plans of care using the nursing processProvide skilled nursing care, including pain and symptom management, medication administration, and treatments per physician ordersEducate and counsel patients, families, and caregivers on disease process, self-care, medications, and comfort measuresAct as Case Manager for assigned patients, coordinating care across physicians, interdisciplinary team members, and community resourcesMaintain accurate, timely clinical documentation, including pain and symptom outcomesCommunicate patient status changes to physicians and obtain orders as neededSupervise hospice aides and delegate care appropriatelyParticipate in interdisciplinary team meetings, on-call rotation, and quality improvement initiativesEnsure a safe care environment and arrange for necessary equipment, supplies, and servicesWe 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":"Hospice LPN (Rhode Island)","City":"Warwick","ExpirationDate":null,"PriorityOrder":0,"Requirements":"Active LPN license in the state of practice (Rhode Island or Compact) Current CPR certificationValid driver?s license with reliable vehicle","Skills":"At least 1 year of hospice nursing experienceFamiliarity with hospice EMR systems and interdisciplinary care models1?2 years of recent acute care nursing experience and 1?2 years of recent home care experience","Industry":"Nurse","Country":"US","Division":"IGH","Office":null,"IsRemoteJob":false,"IsInternalJob":false,"ExtraValues":null,"__RecordIndex":0,"__OrdinalPosition":0,"__Timestamp":0,"Status":null,"ApplicantCount":0,"SubmittalCount":0,"ApplicationToHireRatio":0,"JobDuration":null,"SalaryHigh":34.0000,"SalaryLow":27.2000,"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 Hospice LPN plans, coordinates, and delivers compassionate end-of-life care to patients and families within their homes and community settings. This role performs comprehensive assessments,... develops and manages individualized plans of care, and provides skilled nursing services focused on comfort, symptom management, and quality of life. The LPN serves as a key member of the interdisciplinary hospice team, acting as a patient advocate and clinical resource. As assigned, the nurse functions as a Case Manager, coordinating services and supervising hospice aides to ensure continuity of care. The position requires strong clinical judgment, communication skills, and the ability to work with a team in a facility and in-home setting.Key ResponsibilitiesPerform initial, ongoing, and comprehensive assessments of patients and families to determine hospice needsDevelop, implement, and regularly revise individualized plans of care using the nursing processProvide skilled nursing care, including pain and symptom management, medication administration, and treatments per physician ordersEducate and counsel patients, families, and caregivers on disease process, self-care, medications, and comfort measuresAct as Case Manager for assigned patients, coordinating care across physicians, interdisciplinary team members, and community resourcesMaintain accurate, timely clinical documentation, including pain and symptom outcomesCommunicate patient status changes to physicians and obtain orders as neededSupervise hospice aides and delegate care appropriatelyParticipate in interdisciplinary team meetings, on-call rotation, and quality improvement initiativesEnsure a safe care environment and arrange for necessary equipment, supplies, and servicesWe 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/.

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