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147  Medical Writer Jobs in Hopewell, NJ

Regulatory Affairs Sr. Associate-US

Ortho Clinical Diagnostics, Inc. Raritan, NJ

The RA Sr. Associate will be responsible for coordinating, compiling and submitting regulatory applications to regulatory affiliates worldwide and… CareerBuilder

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Automotive Service Advisor / Ford Customer Service Writer / Auto Sales

Fred Beans Ford Doylestown, PA

• Ford Automotive Service Advisors / Service Writers greet customers and assist them with any inquiries they may have • Automotive Service… CareerBuilder

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Associate Manager; Regulatory Affairs

Professional Resource Partners Port Mercer, NJ

At our global pharmaceutical company, you will contribute to innovative breakthroughs! We are committed to helping people lead longer and healthier… Professional Resource Partners

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Senior Medical Writing Scientist

Johnson & Johnson 100+ Reviews Raritan, NJ

Janssen Research & Development, L.L.C (part of the Johnson & Johnson family of companies), is recruiting for a Senior Medical Writing Scientist… Johnson & Johnson

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Associate Director, Regulatory Affairs Ad & Promo

Celgene 72 Reviews Berkeley Heights, NJ

will include, but are not limited to, the following: • Manage regulatory aspects of Post-Marketing regulatory submissions and communications with the… Ivy Exec

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Sr Statistical Programmer

Novo Nordisk 100+ Reviews Princeton, NJ

with project team members including statisticians, medical writers, data… statisticians and medical writers. GENERAL: This has limited independence.… Beyond.com

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Mommy Jobs Online Remote Staffing Agency

MJOL Princeton, NJ

Please call us today to consult about how we can help you find a work at home job at 14054186160 or send your email inquiries to if you have further… Getit.me

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Sr. Associate, Clinical Publisher

Daiichi Sankyo Inc. 68 Reviews Edison, NJ

Medical Writers on document formatting issues, corrective actions… , Regulatory Operations, Content Management) along with assigned MedicalBeyond.com

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Associate Director, Regulatory Affairs

Celgene 72 Reviews Berkeley Heights, NJ

will include, but are not limited to, the following: 1. Develop and implement global regulatory strategy for assigned projects, along with Regional… Celgene

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SCIENTIFIC WRITER

Bristol Myers Squibb 100+ Reviews Princeton, NJ

of ECG findings, etc), ensuring the coordination and integration of the scientific, medical, and regulatory input from development team members… Beyond.com

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Regulatory Affairs Associate, Non-Steriles

Teva Pharmaceuticals 81 Reviews Horsham, PA

* Interacts with FDA and all Teva sites via written and phone communications. * Approves IIG ingredients and assures that they are in… Beyond.com

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Associate Director, Regulatory Affairs-CMC

Bausch & Lomb / Valeant Pharmaceuticals Bridgewater, NJ

Valeant Pharmaceuticals International, Inc. is a diverse and decentralized pharmaceutical company that is committed to focusing on our key… Beyond.com

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Associate Director, Regulatory Affairs-CMC

Valeant Pharmaceuticals 34 Reviews Bridgewater, NJ

The Regulatory Affairs Associate Director – CMC, independently manages all regulatory CMC aspects of Valeant’s pharmaceutical products throughout… Beyond.com

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Associate Director, Regulatory Affairs

Daiichi Sankyo Inc. 68 Reviews Edison, NJ

We currently have an opening for a Associate Director, Regulatory Affairs in our Edison, New Jersey location. Responsible for managing the… Beyond.com

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SENIOR SCIENTIFIC WRITER

Bristol Myers Squibb 100+ Reviews Princeton, NJ

documents, pharmacometrics reports, responses to Health Authorities), ensuring the coordination and integration of the scientific, medical, and… Beyond.com

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Senior Medical Writing Scientist

J&J Family of Companies Raritan, NJ

** Janssen Research & Development, L.L.C (part of the Johnson & Johnson family of companies), is recruiting for a Senior Medical Writing Scientist… Beyond.com

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Regulatory Affairs Associate, Steriles

Teva Pharmaceuticals 81 Reviews Horsham, PA

* Evaluates changes to regulatory documents and formulates strategies to maintain submission goals. * Interacts with FDA and all Teva… Beyond.com

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GEAR (GCRD) Global Clinical R&D Operations Rotation -

Celgene Corporation 72 Reviews Summit, NJ

will include, but are not limited to, the following: Clinical Trial Analyst: • Supports development of feasibility criteria for clinical… JobsInLogistics

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Regulatory Affairs Associate

Joule' Clinical Horsham, PA

- Preparing regulatory submissions such as ANDAs, amendments, supplements, deficiency responses, and annual reports in accordance to FDA guidelines… CareerBuilder

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