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Site Identification Specialist (Feasibility)


Aline Vandermeeren
Recruiter
+32 497 71 58 10


Job description

We are looking for a relationship pro, dedicated to connecting with sites to advance clinical trials in the best way. 

Office-based in Leuven, with flexibility.

You will: 

  • Constantly maintain and generate relations with Investigative Sites
  • Maintain and refine internal site databases in cooperation with Study Startup, Clinical Operations and Process Improvement.
  • Participate in development of improvement strategies for the site identification process, implementation thereof, as well as related training activities

Project Responsibilities:

  • Define the main study objectives and the optimal site profile
  • Create initial list of potential sites
  • Communicate with project teams on project/ regional level to fine-tune strategy and methodology of initial and follow-up site contacts depending on indication, regional specifics, and technologies in use
  • In cooperation with the project team, maintain a study site identification tracker for further site evaluation and selection activities
  • Liaise with project teams to evaluate status and progress of site identification, to identify and highlight any potential risks or issues to timelines or objectives
  • In cooperation with Legal, perform due diligence check of regulatory and legal limitations applicable to the recommended investigators or clinical sites
  • Participate in project team meetings during study startup, as needed
  • Support the project team throughout study startup and further on, whenever additional rounds of site identification are necessary, and/or additional information on the site/investigator is needed.

Profile

  • University/college degree (Life Sciences/Pharmacy/RN/Healthcare field is a plus), or an equivalent combination of education, training, and experience that presents the required knowledge, skills, and abilities
  • Minimum 2 years of proven prior experience in Site Identification/Study Start-Up activities or equivalent is required
  • Understanding of Good Clinical Practice, local laws and applicable regulations in the region
  • Full working proficiency in English, Dutch and French
  • Communication and collaboration skills
  • Demonstrated ability to work in a dynamic environment under compressed deadlines across several projects, each with unique requirements

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