Planet Pharma jobs in Cambridge, MA

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Process Documentation Writer

Planet Pharma - Cambridge, MA
Summary: ASAP Start Date Responsibilities Responsible for GMP documentation process in support of manufacturing operations including Initiate and revise
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Open Access Lab Technician

Planet Pharma - Cambridge, MA
We are looking for a mechanically skilled candidate to maintain our fleet of open access LC-UV-MS-ELSD analytical instruments. You will be part of an Open
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Clinical Trials Mgmt I

Planet Pharma - Cambridge, MA
Supports and assists Global Clinical Project Leads (CPL) and the Clinical Operations Leads (COL) in operationalizing multiple clinical research studies in an
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Documentation Specialist I

Planet Pharma - Cambridge, MA
Serves as the Sponsor Starting Point Template technical expert in the creation and maintenance of Clinical documents like protocol, amendments, summary of
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Medical Writer III

Planet Pharma - Cambridge, MA
Duties: Work with therapeutic teams to develop and/or edit scientific/clinical documents, including manuscripts, abstracts, posters, and slide presentations
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Sr Manager of Medical Writing

Planet Pharma - Cambridge, MA
The Senior Manager of Medical Writing will primarily be required to independently plan, write, and review clinical and regulatory documents for companies
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Bioinformatics Programmer

Planet Pharma - Cambridge, MA
Job Location - Cambridge, MA. - Contract to possible hire opportunity Develop, and implement using company's proprietary state-of-the-art algorithm
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Associate Director/ Clinical Project Leader

Planet Pharma - Cambridge, MA
The Associate Director, Clinical Project Leader is responsible for and manages study deliverables through internal and external resources and is the primary
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Biostatistician with SAS Programming III

Planet Pharma - Cambridge, MA
Minimum 5 years experiences in the pharma industry and experiences with regulatory submissions. Under the supervision of the project lead statistician,...
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EDC Data Manager/ Clinical Trial Programmer

Planet Pharma - Cambridge, MA
Data Management: Clinical Trial Programmer The Clinical Trial Programmer will be responsible for the database design activities for the entire life cycle of
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