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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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Medical Writer 1

IQVIA

1–3 years

January 27, 2026

Online Application

Lab Project Services Coordinator

IQVIA

0 - 1 Years

January 27, 2026

Online Application

Statistical Programmer

Saama Technologies

2–4 Years

January 27, 2026

Online Application

Statistical Programmer

Tata Consultancy Services (TCS)

3 to 12 Years

January 27, 2026

Online Application

Medical Writer

Kelly SETT

3 years+

January 26, 2026

Online Application

Pharmacovigilance Team Lead

CliniResource

3–5 years

January 26, 2026

Online Application

Dose Surveillance Advisors

Novo Nordisk

2 - 4 Years

January 24, 2026

Online Application

Senior Safety Writer and Project Coordinator

Fortrea

5–7 years

January 24, 2026

Online Application

Pharmacovigilance Officer

Veeda CR

2–3 Years

January 24, 2026

Online Application

Associate STEM Content Analyst

Clarivate

0 - 6 Months

3 - 5 LPA

January 23, 2026

Online Application

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