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Clinical Research Clinical Data Management (CDM)Pharmacovigilance Medical Writing Trial Master File (TMF)Medical Coding SAS Data Sciences Medical Science Liaison (MSL)Medical Reviewer RWE / HEOR

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Clinical Research Clinical Data Management Pharmacovigilance Trial Master File (TMF)Regulatory Affairs Medical Reviewer Medical Coding Pharmacist Medical Devices

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Pharmacovigilance Associate, Pharmacovigilance Specialist, and Senior Pharmacovigilance Specialist

Alvotech

2 - 7Years+

4 - 25 LPA

March 11, 2026

Online Application

Global Feasibility Specialist

Syneos Health

1 year experience in clinical trials

March 11, 2026

Online Application

SAS Programmer

Medpace

1 - 2 Years

March 11, 2026

Online Application

Regulatory Operations Associate

ICON

1 - 3 Years

March 11, 2026

Online Application

Regulatory Affairs Associate

Parexel

2 to 5 years

March 11, 2026

Online Application

TMF Study Lead & Process Lead

Bristol Myers Squibb

3–5 years

March 11, 2026

Online Application

Animal Welfare Compliance Associate II

Labcorp

0 - 3 Years

March 10, 2026

Online Application

Associate Contracts Analyst

IQVIA

Freshers

March 10, 2026

Online Application

Project Analyst eCOA

Clario

2–4 years

March 9, 2026

Online Application

Medical Coding Specialist

ICON

March 9, 2026

Online Application

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