Clinical Project Manager Jobs in Newton, Massachusetts

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New England Research Institutes (NERI) was founded in 1986 and has grown to become a research organization with a global reputation for high-quality research, innovative thinking, and the use of state-of-the-science tools and techniques. NERI continues to be a leader in public health research, clinical trials management, epidemiology, and state of the art media and dissemination research. NERI's ...

Responsibilities : The DMPM manages the end to end clinical data flow (data acquisition from Case Report Form (CRF) to Electronic Submission (ESUB) of Clinical Data) and ensures timely project execution in multiple outsourcing models across multiple study phases and disease indications. Accountable for overall quality of study/program data. Develops risk mitigation or action plans and oversees ex...

CyberCoders Matching Great People with Great Companies Learn more about CyberCoders Clinical Project Manager Boston, MA Full-Time $85,000 - $140,000 Apply Apply Clinical Project Manager Boston, MA Full-Time $85,000 - $140,000 Apply Job Details Great opportunity for a Senior level Clinical Project Manager to work with a growing CRO. This CRO specializes in Oncology and your Oncology ex...

TechData is looking forBiostatistician (one can be remote) and SAS programmers (Some positions can be telecommuting), Quality Assurance Specialist, Quality Control Analyst, , SAP Business Planner, Project Manager/IT, Project Leader for our pharmaceutical clients. Please see below requirements and send your resume to: *****. TechData is a leading provider for temporary and ...

New England Research Institutes (NERI) was founded in 1986 and has grown to become a research organization with a global reputation for high-quality research, innovative thinking, and the use of state-of-the-science tools and techniques. NERI continues to be a leader in public health research, clinical trials management, epidemiology, and state of the art media and dissemination research.NERI's un...

The Clinical Project Manager will be responsible for the oversight and management of our early and late-stage clinical studies. Participate in contract research organization (CRO) qualification and selection Manage CROs and other external vendors supporting clinical studies Independently manage study activities, including: selection of investigators, study start-up activities including site ini...

PRIMARY ROLE: • Serve as clinical operations due diligence team member for assigned due diligence exercises in close partnership with GCDO internal teams to ensure alignment of costs, timings and metrics with Shire standards • Support GCDO due diligence and integration team lead in integration activities to ensure efficient knowledge transfer and efficient integration of acquired assets RESPONS...

Sr. Clinical Project Manager 9869BR R & D Clinical Research and Devel (10000447) Regular MGR United States - MA - Lexington Program Management Clinical Development Operations Primary Duties • Responsible for the planning, implementation, execution and management of one or more clinical research studies. • Manages clinical outsourcing to CROs and other vendors such as IVRS, labs, IRBs, e...

Clinical Operations Project Manager, Due Diligence & Integration 9684BR R & D Clinical Research and Devel (10000447) Regular ASSC DIR United States - MA - Lexington Clinical Development Operations Competitive Intelligence PRIMARY ROLE: • Serve as clinical operations due diligence team member for assigned due diligence exercises in close partnership with GCDO internal teams to ensure alig...

Responsibilities : The DMPM manages the end to end clinical data flow (data acquisition from Case Report Form (CRF) to Electronic Submission (ESUB) of Clinical Data) and ensures timely project execution in multiple outsourcing models across multiple study phases and disease indications. Accountable for overall quality of study/program data. Develops risk mitigation or action plans and oversees ex...

This position can be home based ANYWHERE in MASSACHUSETTS!Our client is currently hiring a SENIOR CLINICAL PROJECT MANAGER, home based. Global experience is preferred. Excellent team looking for someone with good leadership skills, as well as strong clinical research knowledge and understanding. Excellent communication skills necessary. 4years of project management experience is preferred as w...

Responsibilities : The DMPM manages the end to end clinical data flow (data acquisition from Case Report Form (CRF) to Electronic Submission (ESUB) of Clinical Data) and ensures timely project execution in multiple outsourcing models across multiple study phases and disease indications. Accountable for overall quality of study/program data. Develops risk mitigation or action plans and oversees ex...

Job Description About ImmunoGen, Inc. ImmunoGen, Inc. develops targeted anticancer therapeutics. The Company’s ADC technology uses tumor-targeting antibodies to deliver an ImmunoGen cell-killing agent specifically to cancer cells. The Company utilizes its ADC technology with its antibodies to create ImmunoGen product candidates and also out-licenses limited rights to use its technology to other ...

Company Description: Who We Are ImmunoGen, Inc. develops targeted anticancer therapeutics. The Company's ADC technology uses tumor-targeting antibodies to deliver an ImmunoGen cell-killing agent specifically to cancer cells. The Company utilizes its ADC technology with its antibodies to create ImmunoGen product candidates and also out-licenses limited rights to use its technology to other compan...

Please note that the requirements specified in this posting are the basic qualifications required for the Clinical Supply Program Manager; however, job title will be dependent on the candidate’s level of experience in those requirements. OBJECTIVE: As a member, representing Global Clinical Trial Supply Chain (GCTSC) on the l clinical study team, the incumbent plans, establishes and monitors the ...

Please note that the requirements specified in this posting are the basic qualifications required for the Clinical Supply Program Manager; however, job title will be dependent on the candidate’s level of experience in those requirements. OBJECTIVE: As a member, representing Global Clinical Trial Supply Chain (GCTSC) on the l clinical study team, the incumbent plans, establishes and monitors the ...

Clinical Trial Operations Manager-75014026-60562 Description Sanofi, an integrated global healthcare leader, discovers, develops and distributes therapeutic solutions focused on patients’ needs. Sanofi has core strengths in the field of healthcare with seven growth platforms: diabetes solutions, human vaccines, innovative drugs, consumer healthcare, emerging markets, animal health and the new Ge...

Sr Clinical Trial Operations Manager-75012802-60103 Description Sanofi, an integrated global healthcare leader, discovers, develops and distributes therapeutic solutions focused on patients’ needs. Sanofi has core strengths in the field of healthcare with seven growth platforms: diabetes solutions, human vaccines, innovative drugs, consumer healthcare, emerging markets, animal health and the new...

Clinical Trial Operations Manager-75012687-60054 Description Sanofi, an integrated global healthcare leader, discovers, develops and distributes therapeutic solutions focused on patients’ needs. Sanofi has core strengths in the field of healthcare with seven growth platforms: diabetes solutions, human vaccines, innovative drugs, consumer healthcare, emerging markets, animal health and the new Ge...

Baxalta Incorporated (NYSE: BXLT) is a $6 billion global biopharmaceutical leader developing, manufacturing and commercializing therapies for rare and chronic conditions in hematology, oncology and immunology. Driven by passion to make a meaningful impact on patients’ lives, Baxalta’s broad and diverse pipeline includes biologics with novel mechanisms and advanced technology platforms such as...