Instagram
youtube
Facebook

Site Selection Lead

3-5 years
Not Disclosed
10 Dec. 5, 2025
Job Description
Job Type: Full Time Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences 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

Site Selection Lead – Clinical Research

Location: Bangalore, India
Category: Clinical / Clinical Operations
Employment Type: Full-Time
Experience Required: 3–5 years in Clinical Research, Site Selection, or Feasibility Studies

Job Overview

We are seeking a highly skilled Site Selection Lead to oversee the feasibility and site identification process for global clinical trials. The role requires collaboration with cross-functional teams, including global feasibility, start-up, legal, and project management teams, to ensure timely and high-quality site selection aligned with client expectations. This position is based in Bangalore, India, and is ideal for candidates with a strong background in clinical research, site identification, and feasibility studies.

Key Responsibilities

  • Develop initial site lists in coordination with Global Feasibility Leads for feasibility assessment and site identification.

  • Provide full oversight of the site selection process, including survey development, local resource training, site outreach, progress reporting, site selection tools, and client interactions.

  • Evaluate potential site information sources, identify advantages and limitations, and manage timelines to ensure target site numbers are achieved in each region and country.

  • Conduct literature and internet searches to support site performance evaluation and site feasibility assessment.

  • Create and manage electronic surveys using company software, ensuring high-quality data collection and accurate reporting.

  • Collaborate with internal teams to identify risks, out-of-scope activities, and develop contingency plans.

  • Ensure the site identification team updates internal tracking tools accurately and efficiently.

  • Develop and deliver training programs on feasibility and site identification requirements, processes, and best practices.

  • Liaise with global and local cross-functional teams, including clinical, country teams, start-up, legal, and project management.

  • Support audit documentation and presentations related to site identification oversight.

  • Perform additional duties as assigned to ensure the success of clinical site selection initiatives.

Required Qualifications & Experience

  • Education: University or college degree in Life Sciences or related field from an accredited institution.

  • Experience: 3–5 years of experience in clinical research, pharmaceutical companies, or CROs, with demonstrated expertise in site selection, site identification, feasibility studies, and advanced Excel skills.

  • Strong understanding of clinical trial processes and regulatory requirements.

  • Excellent communication, organizational, and analytical skills with attention to detail.

  • Ability to work independently and collaboratively within global cross-functional teams.

  • Proficient in managing multiple priorities and delivering projects on time.

Work Environment & Physical Demands

  • Office-based in Bangalore, India; remote work possible based on business requirements.

  • May involve occasional domestic travel for site visits and cross-functional team collaboration.

  • Work requires extensive use of computers and standard office equipment.