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Sr Ctm (Clinical Trial Medical Advisors)

Gsk Plc
GSK plc
2+ years
Not Disclosed
India
10 March 14, 2026
Job Description
Job Type: Full Time Remote Education: MD/PhD/PharmD 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 Description

Position Summary
The Senior CTM (Clinical Trial Medical Advisor) functions as a field-based scientific expert supporting clinical development programs and clinical trial execution. The role focuses on building strong scientific relationships with investigators and key stakeholders while ensuring accurate protocol understanding and high-quality clinical trial implementation.

This position supports the execution of clinical trials by providing scientific guidance to investigators, assisting with protocol interpretation, and identifying challenges related to trial feasibility, enrollment, and study implementation. The role also acts as a liaison between clinical research sites and internal development teams to ensure effective communication and consistent study conduct.

Key Responsibilities

Develop and maintain strong scientific relationships with principal investigators, sub-investigators, and study physicians

Provide protocol-related scientific support including study rationale, objectives, eligibility criteria, endpoint assessments, and study procedures

Support the implementation of clinical trial protocols by reinforcing critical-to-quality elements and ensuring accurate scientific understanding at study sites

Identify challenges affecting trial execution such as screening failures, enrollment barriers, and endpoint inconsistencies, and communicate insights to internal teams

Provide scientifically grounded input on trial feasibility, patient recruitment strategies, and retention approaches

Capture and communicate investigator insights related to protocol feasibility, clinical practice patterns, and operational challenges

Support scientific components of investigator meetings, presentations, and clinical discussions with investigators and study teams

Participate in scientific conferences or clinical meetings to maintain awareness of evolving therapeutic trends

Ensure compliance with regulatory guidelines including ICH-GCP standards and internal company policies

Maintain accurate documentation of field interactions, scientific exchanges, and investigator feedback in required systems

Professional Experience Requirements

Minimum 2 years of experience in clinical research, clinical development, or clinical trial support

Strong understanding of clinical trial methodology, protocol implementation, and GCP requirements

Experience engaging investigators and physicians in scientific dialogue

Ability to communicate complex clinical information clearly in both small group and large presentation settings

Experience working with cross-functional clinical research teams and external stakeholders

Apply Details

Apply via the company career portal for
Syneos Health