Site Identification Specialist

We are the company that cares – for our staff, for our clients, for our partners and for the quality of the work we do. A dynamic, global company founded in 1995, we bring together 3,000 driven, dedicated and passionate individuals. We work on the frontline of medical science, changing lives, and bringing new medicines to those who need them.

We are in search of an experienced professional dedicated to developing strategic relationships with clinical research sites, with the aim of optimizing and advancing the progress of clinical trials.

This is the main responsibility of a site ID specialist

• Communicate and build relationship with clinical sites to identify potential centres for clinical trials.
• Maintain and refine internal site databases in cooperation with Study Startup, Clinical Operations and Process Improvement

Project Responsibilities:

• Conduct site identification activities, including discussion of clinical trial protocols and collection of site identification questionnaires during the startup phase of the clinical trials.
• 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:

• University/college degree (MD/PharmD degree), or an equivalent combination of education, training and experience
• On-site monitoring experience is a plus
• Understanding of Good Clinical Practice, local laws and applicable regulations in the region
• Demonstrated ability to work in a dynamic environment, under compressed deadlines across several projects, each with unique requirements

Advance your career in clinical research and develop new skillsets whilst growing with the organization.