Site Selection Lead
📍 Location: Bangalore
🏢 Category: Clinical
🆔 Job ID: 252075
Job Overview
The Site Selection Lead is responsible for overseeing the feasibility and site identification process for clinical studies. This role involves site list development, site evaluation, data analysis, survey management, cross-functional collaboration, and ensuring high-quality deliverables aligned with client expectations.
Key Responsibilities
Site Feasibility & Selection
Develop initial site lists in collaboration with the Global Feasibility Lead.
Full oversight of the feasibility/site identification process, including survey development, programming, site outreach, progress reporting, and site selection decisions.
Collaborate with Global Feasibility Leads to collect country and investigator feedback; provide summaries and analysis.
Ensure site identification studies are conducted on time, meeting quality standards and client expectations.
Develop site lists according to program or protocol requirements, working closely with strategy and start-up teams.
Evaluate available sources of potential site information and their advantages/disadvantages.
Manage timelines and adjust target site list requirements to meet predefined goals.
Facilitate identity matching through master data management coordination.
Data Management & Analysis
Perform literature and internet searches for potential sites.
Utilize available data sources to assess site performance.
Create electronic surveys using company software; generate topline or standalone surveys.
Ensure accuracy and quality of survey-driven data.
Enter and update internal tracking tools for site identification.
Cross-Functional Collaboration & Training
Participate in internal planning meetings and client interactions.
Identify potential risks or out-of-scope activities and discuss contingency plans with stakeholders.
Train team members on feasibility and site identification requirements/processes.
Liaise with global cross-functional teams, including legal, start-up, clinical, country teams, and project management.
Contribute to audit presentations and documentation related to site ID oversight.
Other Duties
Perform additional duties as assigned.
Qualifications
Education
University/college degree (preferably in Life Sciences) from an accredited institution.
Experience
Minimum 3–5 years of clinical research experience in a pharmaceutical company, CRO, or equivalent role.
Increasing responsibility in site selection, site identification, and feasibility.
Strong Excel skills and proficiency in data analysis tools.
Equal Opportunity
Fortrea is an Equal Opportunity Employer. Learn more about EEO & Accommodations here.
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