Senior Scientific Writer, Oncology Regulatory Strategy Lead

Pfizer
La Jolla, CA
Org Marketing Statement All over the world, Pfizer colleagues are working together to positively impact health for everyone, everywhere. Each position at Pfizer touches and contributes to the succe...

Posted: 36 days ago

Principal Medical Writer - Regulatory Neuroscience & Pain

AbbVie, Inc
Crown Point, IN
Medical Writing Clinical Operations at AbbVie conducts/manages clinical trials and provides therapeutically aligned, scientific strategy and operations management for the planning, execution and re...

Posted: 41 days ago

Senior Manager Medical Writing & Publications

AbbVie, Inc
Crown Point, IN
Senior Manager Medical Writing and Publications In partnership with the Publications Sub teams of the Global Project Team (GPT), Global Medical Publications drives the strategic planning for the di...

Posted: 42 days ago

Senior Scientific Writer, Oncology Regulatory Strategy Lead

Pfizer
Pearl River, NY
Org Marketing Statement All over the world, Pfizer colleagues are working together to positively impact health for everyone, everywhere. Each position at Pfizer touches and contributes to the succe...

Posted: 36 days ago

Senior Medical Communications Scientist / Senior Medical Writer

Vertex Pharmaceuticals
Boston, MA
The Senior Medical Communications Scientist is responsible for writing and editing Clinical Development documents, including but not limited to clinical protocols, investigator’s brochures, clinical s...

Posted: 28 days ago

Technical Writer

innocom
New Jersey, NJ
Technical Writer – 3972120 Location: Bridgewater NJ In person interview required - This position requires the incumbent to be highly organized, self-motivated, and able to juggle multiple p...

Posted: 11 days ago

KeywordCMC Technical Writer

talentburst_inc
San Francisco, CA
ID-3972120 Job Title: CMC Technical Writer Location-Bridgewater,NJ Duration-6-12 Months contract Duties: Contribute to R&D, LCM and Industrial Development and Innovation projects (in-licensing, ...

Posted: 11 days ago

CMC Documntation Manager

Bristol Myers Squibb
New Brunswick, NJ
As the Manager of CMC Documentation this position involves coordinating filing activities with internal regulatory staff, pursuing and compiling information from scientists, and authoring the CMC sect...

Posted: Today

CMC Documntation Manager

Bristol Myers Squibb
Brunswick, NJ
Description As the Manager of CMC Documentation this position involves coordinating filing activities with internal regulatory staff, pursuing and compiling information from scientists, and aut...

Posted: 6 days ago

CMC Technical Writer – Contract (New Jersey)

JGB BioPharma Consulting
New York, NY
DESCRIPTION: - Contribute to R&D, LCM and Industrial Development and Innovation projects (in-licensing, partnership projects) by planning, writing and delivering agreed submission deliverables for US,...

Posted: 11 days ago

CMC Documntation Manager

R&D - Pharmaceutical Development
New Brunswick, NJ
Description As the Manager of CMC Documentation this position involves coordinating filing activities with internal regulatory staff, pursuing and compiling information from sci...

Posted: 1 day ago

Sr. Scientist/Scientific Writer

Genesis Biotechnology
Houston, TX
Job Description: Invivotek LLC, a member of the Genesis Biotechnology Group, is a Contract Research Organization focusing on phenotypic characterization of genetically modified mice and rats and...

Posted: 14 days ago

Web Writer

Kelly Engineering Resources
Atlanta, GA
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Posted: 28 days ago

Documentation Specialist II

Integrated Project Services, Inc
Lancaster, PA
Position Responsibilities: IPS has an immediate need for a Document Control Specialist II for a client in Lancaster, PA. The Document Control Specialist will be reponsible for: * Processing Records...

Posted: 39 days ago