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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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Bioinformatics Biostatistics Data Science & Analytics Clinical SAS Programming HEOR & Real-World Evidence Medical Writing Scientific Writing Medical Science Liaison

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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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Manufacturing – Downstream Process (DSP)

Intas Pharmaceuticals

2 - 9 Years

July 13, 2026

Walk In Interview

Regulatory Affairs, PDR, AMD (API), Bulk Drugs/CRD (Oncology)

Macleods Pharmaceuticals

2–8 Years

July 13, 2026

Walk In Interview

Clinical Data Specialist | Clinical Data Management Jobs

IQVIA

1-6+ Years

July 13, 2026

Online Application

Pharmacovigilance Associate

Cotec Healthcare

2-6 Years

July 13, 2026

Online Application

Analyst

IQVIA

July 13, 2026

Online Application

Analyst - Scientific Communications & Medical Info

AstraZeneca

3–4 years

July 13, 2026

Online Application

Safety Systems Analyst Level 1| Pharmacovigilance

Premier Research

2–5 years

July 13, 2026

Online Application

Trial Analyst

Clinovis Technologies

0 - 2 Years

July 13, 2026

Email Application

QA, QC, ARD, R&D & Production

SCL Lifesciences Ltd

1–10 Years

July 12, 2026

Walk In Interview

Research Scientist (Fresher)

Molsyns Research

Freshers & 1–3 Years

July 12, 2026

Email Application

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