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Clinical Trial Physician

4-6 years
Not Disclosed
10 June 2, 2025
Job Description
Job Type: Full Time Education: B.Sc./M.Sc/B.Pharm/M.Pharm/Life Science 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

 

Job Title:

Clinical Trial Physician

Job Type:

Full Time

Experience Required:

4 – 6 years

Location:

Heads

Department:

Clinical Science Department

Function:

Clinical Trial Physician

Reports To:

Associate Director, Clinical Science


Position Summary

The Clinical Trial Physician plays a pivotal role in overseeing the medical aspects of clinical trials. This includes providing scientific and medical input across departments, performing medical review tasks, supporting protocol development, and contributing to scientific writing efforts. The role ensures high standards of medical accuracy, compliance, and ethical conduct throughout the clinical development process.


Main Duties & Responsibilities

Document Development & Scientific Writing

  • Develops study-related documents:

    • Study Protocols

    • Informed Consent Forms (ICFs) in collaboration with Clinical Operations and Regulatory

    • Pharmacy Manuals

    • Medical Review Plans

  • Prepares:

    • Scientific presentations and manuscripts

    • Medical and protocol-specific training materials

Medical Expertise & Consultation

  • Provides consultation and expertise on therapeutic areas.

  • Offers strategic guidance on clinical trials and projects.

  • Responds to medical queries from CRAs, Project Managers, Clinical Operations Managers, Investigators, etc.

  • Maintains a study-specific QA log.

Medical Review & Oversight

  • Conducts periodic and real-time medical reviews:

    • Assesses eligibility, efficacy, and safety data.

  • Provides input to Data Management for eCRF development.

  • Addresses urgent medical issues 24/7 as required.

Training & External Engagement

  • Delivers protocol and therapeutic area training (internal and external).

  • Participates in Investigator Meetings and industry conferences.

Regulatory Compliance

  • Adheres to:

    • Company’s Quality and Information Security Management Systems

    • Applicable national/international legislation, including data protection laws

    • ICH-GCP guidelines


Education Requirements

  • Required: Medical Degree (MD)

  • Preferred: MSc, PhD, or specialization in Clinical Development, Medical Affairs, Medical Information, or Pharmacovigilance (PV)


Language Skills

  • Exceptional proficiency in spoken and written English


Key Competencies

  • Deep understanding of clinical trial methodologies and medical terminology

  • Strong medical decision-making and judgment skills

  • Excellent communication and interpersonal skills

  • Solid business acumen and organizational awareness

  • Initiative-driven and team-oriented mindset

  • Innovative and strategic thinker

  • Proficient in IT tools and clinical systems

  • Knowledge of clinical development industry best practices


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