Redbock jobs in Boston, MA

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QA Document Coordinator

Boston, MA
*QA Document Coordinator – Biopharmaceutical Company * Onsite Greater Boston Area – 3-6 Month Contract Duties: Verify master records room index with...
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Clinical Project Manager

Cambridge, MA
\*Local candidates only A pharmaceutical client is currently looking for a CPM's to assist in their clinical trials. This is a 12 month contract minimum with...
Clinical Research
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Scientific Editor/Technical Writer

Cambridge, MA
Scientific Editor – Biopharmaceutical Company Location – Cambridge, MA 6-Month Contract Duties: Work directly with scientists within Early Development...
Technical WritingMicrosoft Office
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Regulatory/CMC Technical Writer

Boston, MA
Regulatory/CMC Technical Writer A biopharmaceutical company in the greater Boston area who is focused on creating transformative therapies for those facing...
Technical WritingProject Management
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Manager of Regulatory Affairs

Cambridge, MA
SUMMARY: * Work with Regulatory Affairs management to define regulatory strategy and to compile and submit, in a timely manner, regulatory documents according...
Project Management
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Associate Director Regulatory Affairs CMC

Cambridge, MA
*Associate Director Regulatory Affairs CMC* Duties: * Lead development and execution of robust global regulatory CMC strategy for assigned program(s) with...
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Sr. Manager, Regulatory Affairs, CMC

Cambridge, MA
Sr. Manager, Regulatory Affairs, CMC – Biopharmaceutical Company 6-Month Contract – Onsite Greater Boston Area Overview Reporting to the Director of...
Regulatory Reporting
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