Director of Clinical Research Jobs in Cambridge
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Search Results - Director of Clinical Research Jobs in Cambridge
Biogen-Cambridge
Job Description
About This Role
Reporting to the Senior Director, Neurodegeneration Research Unit, you will implement and oversee cutting-edge research programs with the aim to discover treatments for people living with Alzheimer’s Disease (AD)...
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Alnylam Pharmaceuticals-Cambridge
influencer of the evolving science supporting the clinical research in the assigned program indications.
Key Responsibilities
The Director, Clinical Scientist will be fully conversant with the fundamental stages and principles of drug development...
Fusion Pharmaceuticals-Cambridge
radiopharmaceutical manufacturing facility to meet supply demand for Fusions growing pipeline of RCs.
Job Summary
The Associate Director of Clinical/Translational Pharmacology and Pharmacometrics will be a key member of the PK/PD/PMX team, responsible for designing...
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Lifelancer-Cambridge
Job Title: Associate Director, Clinical Operations, Immunoassay
Job Location: United States
Job Location Type: Remote
Job Contract Type: Full-time
Job Seniority Level: Director
Why Sarepta? Why Now?
The promise of genetic medicine has arrived...
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AIRNA-Cambridge
AIRNA has received $90 million in Series A financing from world class venture capital firms, including Forbion and Arch Venture Partners, and is headquartered in Cambridge, MA with research operations in Tübingen, Germany.
JOB DESCRIPTION
The Director...
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Integrated Resources, Inc-Cambridge
Job Title: Late Phase Research Project Manager
Location: Cambridge, MA*Onsite
Contract: 10 Months (Possibility of Extension)
Pay Range: $60/Hr. on W2
Job Duties:
We are seeking a highly experienced, organized, and motivated Clinical Study...
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Anumana-Cambridge
researchers, data scientists, software engineers, and commercial teams to drive forward cutting-edge research and develop new models of patient care and Clinical
Applications workflows. You must be a self-starter who thrives in a fast-paced, agile environment...
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Takeda Pharmaceutical-Cambridge
and manage core tasks for Analytical controls for clinical trial material efforts across four main areas: a) GMP review and control for analytical documents; b) Release testing oversight, Stability and Shelf life; c) Reference Standard Management; d) GMP...
Takeda Pharmaceutical-Cambridge
for Analytical controls for clinical trial material efforts across four main areas: a) GMP review and control for analytical documents; b) Release testing oversight, Stability and Shelf life; c) Reference Standard Management; d) GMP Quality Systems Contribute...
Takeda Pharmaceutical-Cambridge
and manage core tasks for Analytical controls for clinical trial material efforts across four main areas: a) GMP review and control for analytical documents; b) Release testing oversight, Stability and Shelf life; c) Reference Standard Management; d) GMP...
Lifelancer-Cambridge
to the Director, Head of Medical Writing. The Associate Director, Medical Writing oversees the development of high-quality clinical regulatory documents. The Associate Director, Medical Writing is also responsible for leading and mentoring team members while...
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Takeda Pharmaceutical-Cambridge
and manage core tasks for Analytical controls for clinical trial material efforts across four main areas: a) GMP review and control for analytical documents; b) Release testing oversight, Stability and Shelf life; c) Reference Standard Management; d) GMP...
Lifelancer-Cambridge
Associate Director, Medical Writing oversees the development of high-quality clinical regulatory documents, including but not limited to, protocols, IBs, CSRs, and clinical sections of submissions. The Associate Director, Medical Writing is also responsible...
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Fusion Pharmaceuticals-Cambridge
Fusion Pharmaceuticals, a member of the AstraZeneca Group, is a clinical-stage oncology company focused on developing next-generation radioconjugates (RCs) as precision medicines.Fusion connects alpha particle emitting isotopes to various targeting...
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Takeda Pharmaceutical-Cambridge
and manage core tasks for Analytical controls for clinical trial material efforts across four main areas: a) GMP review and control for analytical documents; b) Release testing oversight, Stability and Shelf life; c) Reference Standard Management; d) GMP...
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