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Medical Scientist/Sr Medical Scientist (Hyderabad/Bangalore )

Syneos Health
2-8 years
INR 8 LPA – 20 LPA
Bangalore, Hyderabad, India
1 June 11, 2026
Job Description
Job Type: Full Time Education: MBBS/MD Skills: Medical Terminology, mRS and EQ-5D-5L., Narrative Writing, Research & Development

Medical Scientist / Sr. Medical Scientist

Company: Syneos Health
Location: Hyderabad / Bangalore, India
Job ID: 25109128
Employment Type: Full-Time
Work Mode: Office-Based / Hybrid (As Per Project Requirement)
Experience: 2–8+ Years (Depending on Level)

About the Role

Syneos Health is hiring a Medical Scientist / Sr. Medical Scientist to support clinical studies through medical and clinical data review activities. The role involves reviewing patient data, ensuring data quality, identifying protocol deviations, supporting data cleaning activities, and collaborating with Clinical Scientists, Medical Directors, Data Management, and Clinical Operations teams throughout the clinical trial lifecycle.

Key Responsibilities

Clinical Data Review

  • Perform clinical data review as per Data Review Plan (DRP).

  • Identify data discrepancies and issue clinical queries.

  • Review and resolve queries to ensure high-quality clinical data.

  • Ensure timely closure of data issues and discrepancies.

Medical Review Activities

  • Review patient eligibility and enrollment criteria.

  • Assess:

    • Medical History

    • Prior Treatments

    • Study Drug Administration

    • Adverse Events (AE)

    • Serious Adverse Events (SAE)

    • Adverse Events of Special Interest (AESI)

    • Concomitant Medications

    • Safety Laboratory Data

    • Efficacy Assessments

    • End of Treatment (EOT)

    • End of Study (EOS)

    • Survival Data

  • Escalate clinical concerns to Clinical Scientists and Study Medical Directors when required.

Clinical Data Quality & Compliance

  • Ensure data quality and audit readiness.

  • Support clinical compliance and systems validation activities.

  • Monitor site data entry performance and identify root causes of data issues.

  • Drive corrective and preventive actions for recurring data quality concerns.

Stakeholder Collaboration

  • Work closely with:

    • Clinical Scientists

    • Study Medical Directors

    • Clinical Operations Teams

    • Data Management Teams

    • Sponsors

  • Communicate training needs and data quality concerns to project stakeholders.

Study Support Activities

  • Support data reviews before:

    • Interim Analyses

    • Data Cuts

    • DSUR Preparation

    • Investigator Brochures (IBs)

    • Regulatory Requests

    • Database Lock (DBL)

    • Site Close-Out Activities

Additional Responsibilities

  • Support EDC completion training activities.

  • Participate in clinical data review meetings.

  • Prepare presentation materials and study review slides.

  • Assist in patient narrative quality review and QC activities.

  • Identify process improvement opportunities to enhance efficiency and data quality.

Required Qualifications

Education:

  • MBBS

  • MD

  • Pharm.D

  • M.Pharm

  • BDS (Depending on therapeutic area and sponsor requirements)

  • Other relevant Life Science qualifications with strong clinical research experience