We are in search of a Site Identification Specialist (feasibility). This position is open to candidates with similar experience or as CRA (min 3 years), Study Startup specialist or equivalent. Experience in oncology is required.

The hiring company is a dynamic, global CRO with more than 3000 highly dedicated colleagues across the world, mainly focussing on Phase 2 and 3 clinical trials in many different therapeutic areas (Onco, Hemato, Rare Diseases, Infectious Diseases,...)

JOB SCOPE:

You are dedicated to developing strategic relationships with clinical research sites, with the aim of optimizing and advancing the progress of clinical trials.

MAIN RESPONSIBILITIES:

• 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
• 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
• 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

QUALIFICATIONS:

• Master (Life Sciences/Pharmacy/Scientific is a plus), or an equivalent combination of education, training and experience
• Minimum 3 years of proven prior experience in on-site monitoring activities or CRA
• ull professional working proficiency in Dutch and English, professional proficiency in French is an asset
• Understanding of Good Clinical Practice, local laws and applicable regulations in Belgium
• Strong Communication and collaboration skills
• Demonstrated ability to work in a dynamic environment, under compressed deadlines across several projects, each with unique requirements
• Live in Belgium

OFFER:

• Flexible working conditions (hybrid office/home based role)
• Extensive training and supportive team
• Competitive salary and benefits package

CONTACT:

Do you meet most of these requirements and do you see yourself in this role? We would love to hear from you!

Please don't hesitate to apply here or to get in touch with Katleen Broeckhoven at katleen@careforceone.be (attach CV).