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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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Quality Assurance (QA)Quality Control (QC)Pharmaceutical Production R&D & Formulation Pharmaceutical Microbiology Pharmaceutical Packaging Pharmaceutical Warehouse Pharmaceutical Engineering Environmental Health & Safety Effluent Treatment Plant (ETP)Technology Transfer (TDS)

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Trainee Executive – Pharma CRM

Vimta Labs Limited

0–1 year

January 8, 2026

Email Application

Senior TMF Specialist

ICON India

3 years

January 8, 2026

Online Application

Rave Custom Function Programmer

IQVIA

2 years

January 8, 2026

Online Application

Medical Surveillance Specialist

IQVIA

2–6 years

January 8, 2026

Online Application

Safety & Pharmacovigilance Specialists

Syneos Health

1 - 3 Years+

January 8, 2026

Online Application

Senior Regulatory Affairs Associate

Parexel

3 - 6 Years

January 7, 2026

Online Application

Medical Writer & Safety Specialist

Medpace

0 - 2 Years

January 7, 2026

Online Application

Pharmacovigilance Operations Coordinator 1

IQVIA

1 years

January 7, 2026

Online Application

Regulatory Affairs CMC Specialists (3–12 Yrs)

IQVIA

3–12 years

January 7, 2026

Email Application

Associate – Regulatory Affairs

ClinChoice

0–3 years

January 7, 2026

Online Application

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