International Senior Regulatory Affair Specialist $150,000 jobs

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Senior / Clinical Trial Manager – Niche Pharma – New Jersey
i-Pharm Consulting
New Jersey
$140,000 - $160,000 a year
I-Pharm has specific expertise in Clinical Research, Medical Affairs, Regulatory Affairs, Pharmacovigilance, Quality Assurance and Bioinformatics....
Easily apply
Senior / Clinical Project Manager – Niche Pharma – New Jerse...
i-Pharm Consulting
New Jersey
$150,000 - $160,000 a year
I-Pharm has specific expertise in Clinical Research, Medical Affairs, Regulatory Affairs, Pharmacovigilance, Quality Assurance and Bioinformatics....
Easily apply

Director, Therapeutic Area Lead, Global Regulatory Affairs,...

King of Prussia, PA
Director Therapeutic Area Lead, Global Regulatory Affairs, Global Product Strategy:. Additionally, provide strategic and tactical regulatory leadership and...

Therapeutic Area Lead Immunology, Global Regulatory Affairs,...

King of Prussia, PA
Director Therapeutic Area Lead, Global Regulatory Affairs, Global Product Strategy:. Additionally, provide strategic and tactical regulatory leadership and...

Associate Director/ Director - Clinical Project Management –...

i-Pharm Consulting
Home Based
$145,000 - $175,000 a year
I-Pharm has specific expertise in Clinical Research, Medical Affairs, Regulatory Affairs, Pharmacovigilance, Quality Assurance and Bioinformatics....
Easily apply

Director, Corporate Reputation-Financial Services--Strategic...

New York, NY 10005 (Financial District area)
Certified turnaround professionals, forensic accountants, corporate investigation specialists, intellectual property specialists, former political leaders,...

Associate / Medical Director, Drug Safety Surveillance, Rare...

Brisbane, CA
Global Regulatory Affairs Lead, Medical Affairs Medical Director, Medical Affairs Study Management, Core Team Lead, BioMetrics, Clinical Pharmacology and Safety...

Medical Director / Senior Scientific Director, U.S. Medical...

Lake County, IL
Provides specialist medical/scientific strategic and operational input into core medical affairs activities such as:....

Group Medical Director, gRED ECD Oncology

South San Francisco, CA
Oversees or directs clinical science input for completion and submission of regulatory filings and other regulatory documentation....
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