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
Employee Name / Line Manager:
Signature:
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