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Senior Medical Scientist (Gurgaon/Hyderabad)

Syneos Health
Syneos Health
3-5 years
upto 9 LPA
Gurugram, India
9 April 30, 2026
Job Description
Job Type: Remote Education: B.Pharm, M.Pharm, Pharm D., BSc., MSc., Lifesciences graduate Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Senior Medical Scientist – Clinical Development Jobs in Gurgaon / Hyderabad | Syneos Health Careers India

Company: Syneos Health
Job Role: Senior Medical Scientist
Location: Gurugram, Haryana / Hyderabad, Telangana, India
Job Type: Full-Time
Work Mode: Office-Based / Hybrid
Experience Required: 3–6 Years
Eligibility: Experienced Professionals Only (Freshers Not Eligible)


About Syneos Health

Syneos Health is a globally recognized, fully integrated biopharmaceutical and life sciences organization focused on accelerating customer success across the drug development and commercialization journey. The company partners with healthcare innovators worldwide to simplify clinical development, improve patient outcomes, and drive scientific advancement in the pharmaceutical and biotechnology sectors.

With a strong presence in clinical research, medical affairs, pharmacovigilance, and regulatory services, Syneos Health offers professionals the opportunity to work on cutting-edge global clinical trials and healthcare solutions.


Job Overview

Syneos Health is hiring experienced professionals for the position of Senior Medical Scientist in Gurgaon and Hyderabad. The role involves providing scientific and clinical support for early and late-stage clinical development programs while ensuring data integrity, protocol compliance, and successful execution of clinical trials.

The selected candidate will collaborate closely with Medical Directors, Clinical Operations teams, Data Management professionals, Drug Safety teams, and Project Management stakeholders to support high-quality clinical research activities.


Key Responsibilities

  • Collaborate with Medical Directors to develop Medical Management Plans, Medical Data Review Plans, and Eligibility Review Plans

  • Perform ongoing and ad-hoc medical reviews of clinical trial data, listings, and visualizations

  • Identify data trends, protocol deviations, subject safety concerns, and potential risks during clinical studies

  • Create and review medical data queries while ensuring timely query resolution

  • Support patient profile review, scientific data analysis, and preparation of Medical Review Summary reports

  • Participate in medical review meetings, safety review discussions, and audit activities

  • Coordinate with Clinical Operations, Data Management, Pharmacovigilance, and Project Management teams

  • Ensure compliance with ICH-GCP guidelines, data privacy standards, SOPs, and global regulatory requirements

  • Monitor project deliverables, timelines, and quality standards for clinical development programs

  • Support internal and external stakeholders during medical review and clinical trial activities


Required Qualifications

  • Advanced qualification in Life Sciences, Pharmacy, Medicine, Clinical Research, or related healthcare discipline

  • Minimum 3–6 years of experience in Clinical Research, Medical Review, Medical Monitoring, Drug Development, or related domains

  • Strong understanding of clinical trial protocols, medical data review, and clinical development processes

  • Working knowledge of ICH-GCP guidelines, pharmacovigilance practices, and regulatory compliance

  • Excellent analytical thinking, communication skills, and stakeholder management abilities


Skills Preferred

  • Clinical Data Review

  • Medical Monitoring

  • Clinical Trial Management

  • Drug Safety & Pharmacovigilance

  • Risk Identification & Medical Analysis

  • Scientific Documentation

  • Regulatory Compliance

  • Cross-Functional Collaboration


Why Join Syneos Health?

  • Opportunity to work with one of the leading global clinical research organizations

  • Exposure to international clinical trials and innovative healthcare programs

  • Strong career growth and professional development opportunities

  • Collaborative and science-driven work culture

  • Involvement in studies supporting FDA-approved and EMA-authorized products

Over the past five years, Syneos Health has contributed to:

  • 94% of Novel FDA Approved Drugs

  • 95% of EMA Authorized Products

  • 200+ Clinical Studies

  • 73,000+ Clinical Trial Sites

  • 675,000+ Trial Patients Globally


Important Note for Applicants

This position is intended for experienced professionals with prior exposure to clinical development, medical review, or related healthcare research domains. Freshers are advised to apply for entry-level Clinical Research, Pharmacovigilance, Drug Safety Associate, or Medical Writing opportunities before targeting senior-level medical scientist roles.


How to Apply

Interested candidates can apply through the official careers page of Syneos Health or explore more verified global pharmaceutical, clinical research, pharmacovigilance, and healthcare job opportunities on ThePharmaDaily.com.