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Global Feasibility Lead

Gsk Plc
GSK plc
3+ years
Not Disclosed
Gurugram, India
10 March 14, 2026
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 Description

Position Summary
The Global Feasibility Lead is responsible for supporting global clinical trial feasibility activities by conducting research, analyzing data, and developing strategies for country and site selection. The role focuses on evaluating clinical trial protocols, identifying potential study sites, and assessing recruitment feasibility to support proposal development and clinical trial planning.

This position works closely with internal stakeholders including business development teams, medical directors, and proposal analysts to review sponsor requirements and ensure feasibility assessments are aligned with study objectives and timelines.

Key Responsibilities

Conduct feasibility assessments for clinical trials by analyzing protocol requirements, patient populations, and site capabilities

Review sponsor requirements and protocols for Requests for Proposals (RFPs) and Requests for Information (RFIs)

Research scientific literature and internal data sources to gather insights related to patient availability, clinical trial landscapes, and disease prevalence

Develop country and site-level feasibility strategies to support clinical trial proposals

Collaborate with internal stakeholders including business units, business development teams, medical directors, and business analysts

Prepare feasibility reports, presentations, and documentation for internal and external stakeholders

Support bid defense meetings and teleconferences by preparing feasibility-related materials when required

Maintain comprehensive records of feasibility research and store relevant data within internal systems

Identify potential challenges related to recruitment, enrollment, and protocol implementation and propose solutions

Support development and improvement of feasibility analysis systems and internal data management tools

Participate in evaluation of clinical trial informatics technologies such as registry search tools and enrollment modeling platforms

Professional Experience Requirements

Experience in clinical trial feasibility analysis, clinical research operations, or clinical development support

Strong understanding of clinical trial processes, site selection strategies, and protocol feasibility assessments

Experience working with feasibility data, clinical trial registries, and enrollment modeling tools

Ability to conduct independent research and analyze scientific literature

Strong written and verbal communication skills in English

Apply Details

Apply via the company career portal for
Syneos Health