Pharmaceutical Industry

Pharmaceutical Industry Jobs

Overview

The pharmaceutical industry is defined as the discovery, development, and manufacture of drugs and medications. It's widespread, including research, chemicals, and the regulation and involvement of government agencies.
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Regulatory Medical Writer at GForce Life Sciences

Plainsboro, NJ | Full Time
$99k-124k (estimate)
6 Months Ago

Medical Writer at Mindlane

Titusville, NJ | Full Time
$98k-124k (estimate)
6 Months Ago

Pharmacist at Actalent

West Chester, OH | Other
$145k-162k (estimate)
8 Months Ago
Job Title: Pharmacist. Job Description. We are seeking an Audit Pharmacist to work 6 hours per week. The ideal candidate must hold both Kentucky and Ohio pharmacist licenses. This position is perfect for someone looking to gain more exposure in the pharmaceutical industry while maintaining another full-time job. Responsibilities. Maintain all appropriate record keeping and licensing in compliance with state and federal pharmacy regulations. Revie...

Pharmaceutical Consultant at Augment Jobs

Austin, TX | Full Time
$52k-63k (estimate)
0 Months Ago
Job Title: Pharmaceutical Consultant. Job Overview. We are seeking an experienced Pharmaceutical Consultant to provide expert guidance and support on drug development, regulatory compliance, and market strategies. The ideal candidate will have a strong background in the pharmaceutical industry and be adept at translating complex information into actionable recommendations. Responsibilities. Advise pharmaceutical companies on drug development and ...

Associate Director, Compliance (US) at SERB Pharmaceuticals

Conshohocken, PA | Full Time
$147k-185k (estimate)
6 Months Ago

Associate Director, Compliance (US) at SERB Pharmaceuticals

Conshohocken, PA | Full Time
$147k-185k (estimate)
6 Months Ago

Associate Director, Compliance (US) at SERB Pharmaceuticals

Conshohocken, PA | Full Time
$147k-185k (estimate)
6 Months Ago

Medical Representative at AstraZeneca

Boston, MA | Full Time
$84k-111k (estimate)
7 Months Ago

Senior Director, Regulatory Affairs at Clinical Resource Network (CRN)

Florham Park, NJ | Full Time
$182k-232k (estimate)
8 Months Ago
Our client is looking to fill the role of Senior Director, Regulatory Affairs. Salary : $250-$280k. Responsibilities. Serve as head for all regulatory activities for US products and to lead, manage and submit regulatory submissions to FDA to include supplements and post-approval reporting of marketed products. Lead all activities related to promotional, advertisements and labeling. Serve as FDA liaison regarding submissions and communications. Le...

Associate Director of Clinical Data Management at Alira Health

Boston, MA | Full Time
$164k-222k (estimate)
8 Months Ago
Join our global team dedicated to innovation and initiative, where physical walls and different time zones don’t limit, but encourage, collaboration. Where all contributions and new ideas are explored with an open mind and work is driven by our shared values : be courageous, be accountable, be honest, be inclusive and elevate others.Job Description SummaryThe Associate Director of Clinical Data Management leads and drives the DM team, acting as m...

Senior Medical Writer at Nucleus Global

Morrisville, PA | Full Time
$118k-146k (estimate)
8 Months Ago
Publication Senior Medical Writer. US - Office based, hybrid or remote. Nucleus Global is an exciting leader in the field of medical communications. Drawn together from several backgrounds including the pharmaceutical industry, research, marketing, medical and regulatory writing, sales, publishing, digital media and design, we have the experience and all-round ability to conceive and deliver the best quality medical communications programs. Our s...

Principal Medical Writer at UroGen

Princeton, NJ | Full Time
$103k-129k (estimate)
10 Months Ago
Job Summary. The Principal Medical Writer (MW) provides MW leadership and subject matter expertise to cross-functional project teams and drives the efficient development of study-level and program-level clinical regulatory documents. She or he is a strategic thinker and decision maker who effectively collaborates with internal and external stakeholders to coordinate document content, quickly resolve conflicts, and meet established timelines. Duti...
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