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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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Interview Preparation

Browse all 35 departments →

Clinical & Safety

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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Regulatory Specialist, Portfolio Acceleration and Analytics

BMS

August 10, 2026

Online Application

Senior Associate Safety Data Analyst

Amgen

2 years+

August 10, 2026

Online Application

Medical Writer

Accenture

3–8 years

August 10, 2026

Online Application

Data Coordinator

Clario

2 years of data processing or clinical data experience

August 10, 2026

Online Application

Associate Healthcare AI Validation & Quality Assurance

OrbiThrust Consulting Pvt Ltd.

August 10, 2026

Email Application

Cardiac Specialist

Clario

1–2 years

August 10, 2026

Online Application

Meta Description: hiring 2026 for Programmer Analyst II and Feasibility Site Specialist roles in India. Check eligibility and apply online.

Thermo Fisher Scientific

0 - 5 Years

August 10, 2026

Online Application

Regulatory Submissions Coordinator (Senior)

Medpace

4 years

August 7, 2026

Online Application

Risk Surveillance Lead

Novartis

Minimum 4 Years

August 7, 2026

Online Application

Health Economics Associate – Modelling

Parexel

Relevant experience preferred (Programming/Health Economics advantageous)

August 7, 2026

Online Application

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