Company Logo

ICON plc

Site Selection Specialist

09 September 2025

Full-Time Osaka

Department

Health & Biotech

Job Category

Health & Biotech

Description

  • Work with the Site Selection Lead to ensure knowledge of the goals, scope and requirements of the project (e.g. number of sites required/country, number of positive responses required etc.) and ensure that high quality results are delivered.
  • Identify study investigators/ sites for potential study participation, both from the database and other potential sources such as local intelligence/internet etc. Ensure all newly identified sites are data based appropriately, checked for quality status and are fully processed.
  • To contact and build relationships with study investigators/ sites and networks in assigned areas (e.g. region(s), countries I countries or therapeutic area) for the conduct of feasibility and potential study participation.
  • To perform phone selection visits, if required.
  • To liaise with country managers to gather country specific evidence to support Site Selection, e.g. site list review, country specific profile of sites, standard of care.
  • To ensure that all data collected, in the conduct of Site Selection or site related country feasibility, is fully documented and kept up to date in relevant systems to build knowledge and intelligence.
  • To ensure appropriate procedures are followed, whether Sponsor specific or according to ICON SOPs, Site Selection RACI.
  • Ensure appropriate follow up with sites on any inconsistencies in data provided for analysis and to chase outstanding feasibility data to ensure a complete data set.
  • To contact investigators, local ICON employees and collect data to support country choice in the conduct of feasibility assessments.
  • To become a country expert on the investigator profile, healthcare setting, standard of care to ensure the best sites are approached for projects.
  • To liaise cross-functionally with other departments such as Study Start Up, CRA management to get local intelligence on sites and support local data collection.
  • Be an expert on how to interact with sites and obtain relevant information to support Site Selection.
  • Use knowledge and experience to build efficiency in the process and consistently deliver high quality investigators, sites, and other data to the Functional Lead for your projects.
  • Ensure debarred Investigators are not included in feasibilities or for study participation.
  • Ensure relevant parties, such as Site Selection lead, Feasibility Manager or Project Manager are aware of any Audit or Regulatory findings that may influence reasons for site selection.
  • Ensure confidentiality is maintained or appropriate confidentiality agreements are in place prior to study discussions.
  • Ensure all investigator feedback and status of contact with the site is tracked and data based appropriately, including reasons for site selection /de-selection.
  • Support other team members, e.g. seconded CRAs, on how to get the best information from sites, act as a trainer and mentor to new staff within the group.
  • Identify high performing sites and develop relationships with them as a single point of contact during site selection and ensure that key data collected from/related to these sites are maintained in ICON's systems.
  • Deliver high quality standards and strive for excellence, act in a proactive, flexible and responsive manner to both internal and external customer needs.
  • Establish good relationships internally and externally.
  • To undertake other reasonably related duties as may be assigned from time to time.
  • Recognize, exemplify and adhere to ICON's value, which centers around our commitment to People, Clients and Performance.
  • To embrace and contribute to our culture of process improvement with a focus on accelerating concept to cure.
  • Travel (approximately 10%) domestic and/or international, as required.
  • Responsible for implementing the project-specific Site Selection strategy at the country level.

Qualifications

  • Bachelor's Degree
  • 0-3 years of experience in a Clinical Research environment
  • Good communication skills
  • Good judgment and decision making
  • Proficient computer knowledge
  • Proficiency in English language is mandatory

Featured Recruiters