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Jun 24, 2026

Woonsocket, RI

|

Accounts Payable

|

Contract

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$52 - $65 (hourly estimate)

{"JobID":544820,"JobType":["Contract"],"EmployerID":null,"Location":{"Latitude":-71.5015,"Longitude":42.0016,"Distance":null},"State":"Rhode Island","Zip":"02895","ReferenceID":"BOS-f03ed623-5cd4-4888-9e72-585785b6860c","PostedDate":"\/Date(1782301054000)\/","Description":"Insight Global is sourcing for a Product Manager with recent AI experience to join a leading health solutions company that provides healthcare and retail pharmacy services. This position will be a bridge between technical and functional with emphasis on ability to manage the product at hand. This role will be in support of a new product platform, measuring marketable insights for the CMO organization. This is a senior level opening, where the Product Manager will be responsible for creating roadmaps, strategy, and communicating cross functionally with various stakeholders. Data Science background is an absolute must have, as well as recent AI experience and ability to develop and drive prototypes. This position is fully remote within the US, with opportunity for extension or conversion.Compensation: $_50_/hr. to $_60_/hr. Exact compensation may vary based on several factors, including skills, experience, and education. Benefit packages for this role will start on day one of employment and include medical, dental, and vision insurance, as well as HSA, FSA, and DCFSA account options, and 401K retirement account access with employer matching. Employees in this role are also entitled to paid sick leave and/or other paid time off as provided by applicable law.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":"Product Manager-AI","City":"Woonsocket","ExpirationDate":null,"PriorityOrder":0,"Requirements":"-Product Management experience, ability to guide cross functional teams strategically and develop product roadmap-Previous experience as a Data Scientist, previous experience with SQL and Python. -AI prototyping experience using Claude and/or VertexAI-Strong analytics and marketing background, experience partnering across analytics, marketing, engineering, etc. using insights generated for actionable outcomes -Excellent communication skills, ability to bridge gap between technical and functional teams. As well as, presenting to stakeholders and executives -Product Management certifications or fundamentals and best practices","Skills":"Preferred Qualifications:Experience with or certifications in Salesforce (SFDC)Experience working in cross-functional, matrixed environmentsTrack record of driving measurable business impact through analyticsSuccess Profile:Strategic thinker who challenges the status quoHighly proactive and solution-orientedStrong communicator who simplifies complexityAble to lead workstreams independently and drive outcomes","Industry":"Accounts Payable","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":65.0000,"SalaryLow":52.0000,"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 sourcing for a Product Manager with recent AI experience to join a leading health solutions company that provides healthcare and retail pharmacy services. This position will be a... bridge between technical and functional with emphasis on ability to manage the product at hand. This role will be in support of a new product platform, measuring marketable insights for the CMO organization. This is a senior level opening, where the Product Manager will be responsible for creating roadmaps, strategy, and communicating cross functionally with various stakeholders. Data Science background is an absolute must have, as well as recent AI experience and ability to develop and drive prototypes. This position is fully remote within the US, with opportunity for extension or conversion.Compensation: $_50_/hr. to $_60_/hr. Exact compensation may vary based on several factors, including skills, experience, and education. Benefit packages for this role will start on day one of employment and include medical, dental, and vision insurance, as well as HSA, FSA, and DCFSA account options, and 401K retirement account access with employer matching. Employees in this role are also entitled to paid sick leave and/or other paid time off as provided by applicable law.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/.

Jul 24, 2026

Largo, FL

|

Architect (Engineering)

|

Perm

|

$170k - $220k (estimate)

{"JobID":556319,"JobType":["Perm"],"EmployerID":null,"Location":{"Latitude":-82.78,"Longitude":27.9,"Distance":null},"State":"Florida","Zip":"33771","ReferenceID":"DGO-947ccb97-9e66-4044-ac27-aed51726624e","PostedDate":"\/Date(1784905616000)\/","Description":"About the Role:The Sr. Director, Clinical Systems leads the strategy, roadmap, delivery, and optimization of all clinical technology products across 100+ clinics, drives clinical workflow optimization, and ensures clinical systems directly support Medicare VBC performance. This role operates a true product organization?combining product management, clinical informatics, UX, engineering, and release management to deliver high-value, user-centered clinical solutions.The ideal candidate drives innovation across the clinical ecosystem by introducing automation, AI-enabled workflows, data-driven analytical models, and digital tools that enhance documentation, streamline ordering, and support proactive, team-based care models.Key Responsibilities:Clinical Application Ownership?Serve as system owner for eCW and all clinical applications.?Manage configuration, upgrades, releases, patches, and environment strategy.?Maintain application roadmaps aligned to clinical and operational priorities.?Oversee eCW and clinical technology vendor relationships and SLAs.Workflow Optimization \u0026 Provider Experience?Design efficient, standardized clinical workflows in partnership with clinical leadership.?Reduce provider burden through documentation, ordering, and charting optimization.?Improve clinic throughput and care team efficiency.?Support adoption through training, change management, and feedback loops.Value-Based Care Enablement?Enable tools for risk adjustment, gaps in care closure, care management, and population health.?Support improvement of HEDIS, STAR ratings, and VBC performance.?Partner with analytics on predictive insights, risk stratification, and proactive outreach.?Introduce automation and AI to reduce administrative burden.Implementation \u0026 Change Delivery?Lead new module implementations, enhancements, and feature rollouts.?Oversee requirements, testing, training, and go live support.?Ensure validated, compliant, safe change delivery in partnership with PMO.Integration \u0026 Interoperability?Define clinical data and workflow requirements for interfaces.?Support integrations with labs, imaging, pharmacy, care coordination, patient engagement, RCM, HR, and SCM systems.?Ensure interoperability standards (HL7, FHIR) and validate clinical data flows.Clinical Data Quality \u0026 Documentation?Ensure accurate, complete, compliant clinical documentation.?Maintain templates, order sets, smart tools, and structured data elements.?Partner with coding, RCM, and compliance to reduce documentation errors.?Support clinical quality reporting and regulatory submissions.Provider \u0026 Clinic Support?Provide Tier 2/3 support for eCW and clinical applications.?Serve as primary point of contact for clinical system issues across 100+ clinics.?Train providers and maintain super user networks.Governance \u0026 Compliance?Participate in clinical governance committees.?Ensure systems support clinical safety, regulatory compliance, and accreditation.?Maintain audit trails, access controls, and data integrity.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":"Sr. Director, Clinical Systems","City":"Largo","ExpirationDate":null,"PriorityOrder":0,"Requirements":"?12+ years of progressive leadership experience in clinical systems, clinical informatics, or healthcare technology.?Demonstrated success designing and optimizing clinical workflows across large, distributed clinic networks.?Experience partnering with clinical leadership (CMO, market medical directors, nursing leaders) to drive adoption and operational change.?Strong background in interoperability (HL7, FHIR), integrations, and clinical data flows.?Experience leading automation, AI-enabled workflows, or digital health innovations that reduce provider burden.?Track record of managing large-scale EMR upgrades, rollouts, and multi-site implementations.?Experience overseeing clinical data quality, documentation standards, and regulatory compliance.? Executive-level communication and stakeholder management skills.?Experience in defining \u0026 executing digital strategy and roadmap across various domains","Skills":"?Deep expertise with EMR/EHR platforms, ideally eClinicalWorks (eCW) in a multi-clinic environment.?Proven experience supporting value-based care, Medicare Advantage, or population health programs.","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":220000.0000,"SalaryLow":170000.0000,"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)\/"}

About the Role:The Sr. Director, Clinical Systems leads the strategy, roadmap, delivery, and optimization of all clinical technology products across 100+ clinics, drives clinical workflow... optimization, and ensures clinical systems directly support Medicare VBC performance. This role operates a true product organization?combining product management, clinical informatics, UX, engineering, and release management to deliver high-value, user-centered clinical solutions.The ideal candidate drives innovation across the clinical ecosystem by introducing automation, AI-enabled workflows, data-driven analytical models, and digital tools that enhance documentation, streamline ordering, and support proactive, team-based care models.Key Responsibilities:Clinical Application Ownership?Serve as system owner for eCW and all clinical applications.?Manage configuration, upgrades, releases, patches, and environment strategy.?Maintain application roadmaps aligned to clinical and operational priorities.?Oversee eCW and clinical technology vendor relationships and SLAs.Workflow Optimization & Provider Experience?Design efficient, standardized clinical workflows in partnership with clinical leadership.?Reduce provider burden through documentation, ordering, and charting optimization.?Improve clinic throughput and care team efficiency.?Support adoption through training, change management, and feedback loops.Value-Based Care Enablement?Enable tools for risk adjustment, gaps in care closure, care management, and population health.?Support improvement of HEDIS, STAR ratings, and VBC performance.?Partner with analytics on predictive insights, risk stratification, and proactive outreach.?Introduce automation and AI to reduce administrative burden.Implementation & Change Delivery?Lead new module implementations, enhancements, and feature rollouts.?Oversee requirements, testing, training, and go live support.?Ensure validated, compliant, safe change delivery in partnership with PMO.Integration & Interoperability?Define clinical data and workflow requirements for interfaces.?Support integrations with labs, imaging, pharmacy, care coordination, patient engagement, RCM, HR, and SCM systems.?Ensure interoperability standards (HL7, FHIR) and validate clinical data flows.Clinical Data Quality & Documentation?Ensure accurate, complete, compliant clinical documentation.?Maintain templates, order sets, smart tools, and structured data elements.?Partner with coding, RCM, and compliance to reduce documentation errors.?Support clinical quality reporting and regulatory submissions.Provider & Clinic Support?Provide Tier 2/3 support for eCW and clinical applications.?Serve as primary point of contact for clinical system issues across 100+ clinics.?Train providers and maintain super user networks.Governance & Compliance?Participate in clinical governance committees.?Ensure systems support clinical safety, regulatory compliance, and accreditation.?Maintain audit trails, access controls, and data integrity.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/.

Jun 05, 2026

Malvern, PA

|

Engineering (Non IT)

|

Contract

|

$40 - $50 (hourly estimate)

{"JobID":538456,"JobType":["Contract"],"EmployerID":null,"Location":{"Latitude":-75.51,"Longitude":40.03,"Distance":null},"State":"Pennsylvania","Zip":"19355","ReferenceID":"PHL-ef4b1ce8-81e4-4900-81df-14becc904134","PostedDate":"\/Date(1780689393000)\/","Description":"One of our large pharmaceutical clients is looking to hire a Sr Quality Specialist to join the EQ team. The individual will provide QA support for TAR-200 (including UPC) and TAR-210 projects, ensuring adherence to quality assurance processes and compliance with all company policies and procedures. They will perform assigned duties and collaborate with cross-functional teams to maintain regulatory standards, facilitate communication within the core team, and help to ensure that all quality-related activities project goals and deadlines are met. In particular, the specific tasks required on a daily basis by the position are:Support, review/pre-review, and/or approve the following --Batch record review -Quarantine shipment (Q-ship) activities-Release for Further Processing (RFFP) activities -EM Quality Events-EM CAPAs-EM Change Controls-EM Planned Deviations -EM Product Quality Complaints -EM Protocols-EM Risk Assessments-EM Electronic Batch Record (eBR) changes-EM Manufacturing Process Instruction (MPI) changes -EM equipment specific Master Validation Plan (MVP) changes-Sterilization-specific documentation -New equipment qualification documentation Own/support the following -Own Child records for Change Controls in TrackWise -Own/support internal Nonconformances (NC) in Comet-Own/support internal Investigations in Comet-Own/support internal Supplier Investigations in CometHelp maintain/manage/keep organized the following-Outstanding EM issues-Transfer of document to the EM-Status of Clinical Trial Material (CTM) lots/production schedule-Various workstreams (help build templates, flowcharts, etc.)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":"Quality Specialist","City":"Malvern","ExpirationDate":null,"PriorityOrder":0,"Requirements":"Bachelor Graduate in Biology, option Biomedical Research Minimum 5-10 years of experience working with pharmacuteical manuafcturng and/or medical devices Minimum 3-5 years of experience working with external partners, preferably CMO partnerships Expertise handing review and approval of batch record review, RFFP acitivites, CAPAs, Change Controls, deviations, quality product compliants, and risk assessmentsTrackwise or Comet experienceExcellent verbal and written communication skills, including ability to effectively communicate with internal and external customers. Excellent computer proficiency e.g MS Office, TrackWise, Minitab Excellent analytical skill to identify gaps and root causes of issues and think out of the box to develop a solution. Ability to work independently with minimum supervision to meet tight deadlines and maintain a positive attitude.","Skills":"Experience with small molecule new product launches","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":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)\/"}

One of our large pharmaceutical clients is looking to hire a Sr Quality Specialist to join the EQ team. The individual will provide QA support for TAR-200 (including UPC) and TAR-210 projects,... ensuring adherence to quality assurance processes and compliance with all company policies and procedures. They will perform assigned duties and collaborate with cross-functional teams to maintain regulatory standards, facilitate communication within the core team, and help to ensure that all quality-related activities project goals and deadlines are met. In particular, the specific tasks required on a daily basis by the position are:Support, review/pre-review, and/or approve the following --Batch record review -Quarantine shipment (Q-ship) activities-Release for Further Processing (RFFP) activities -EM Quality Events-EM CAPAs-EM Change Controls-EM Planned Deviations -EM Product Quality Complaints -EM Protocols-EM Risk Assessments-EM Electronic Batch Record (eBR) changes-EM Manufacturing Process Instruction (MPI) changes -EM equipment specific Master Validation Plan (MVP) changes-Sterilization-specific documentation -New equipment qualification documentation Own/support the following -Own Child records for Change Controls in TrackWise -Own/support internal Nonconformances (NC) in Comet-Own/support internal Investigations in Comet-Own/support internal Supplier Investigations in CometHelp maintain/manage/keep organized the following-Outstanding EM issues-Transfer of document to the EM-Status of Clinical Trial Material (CTM) lots/production schedule-Various workstreams (help build templates, flowcharts, etc.)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/.

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