PSI CRO is hiring a

Site Identification Specialist (Feasibility)

Pretoria, South Africa
Full-Time

Our team is searching for a relationship pro, dedicated to connecting with sites to advance clinical trials in the best way. Sounds like you're the expert we're searching for? 

Hybrid in Pretoria

You will: 

  • 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 the 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.
  • University/college degree (Life Sciences/Pharmacy/RN/Healthcare field is a plus), or an equivalent combination of education, training and experience.
  • Minimum 10 years of proven prior experience in Site Identification/Feasibility/Study Start-Up activities/Site Monitoring.
  • Understanding of Good Clinical Practice, local laws and applicable regulations in the region.
  • Full working proficiency in English.
  • Communication and collaboration skills.
  • Demonstrated ability to work in a dynamic environment, under compressed deadlines across several projects, each with unique requirements.

We offer:

  • Excellent working conditions.
  • Extensive training and friendly team.
  • Competitive salary and benefits package.

Make the right call and take your career to a whole new level. Join the company that focuses on its people and invests in their professional development and success.

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