Site Identification Specialist

Benefits

Additional Information

Please provide your CV in English. The scope of responsibilities will include: Constantly maintain and generate relations with Investigative Sites; Maintain and refine the internal site database in cooperation with Study Startup, Clinical Operations and Process Improvement; Participate in development of improvement strategies for the site identification process; Create the initial list of potential sites; Communicates with project teams to define strategy and methodology of initial and follow-up site contacts; In cooperation with the project team maintain a study site identification tracker; 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; Perform due diligence check of regulatory 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. University/college degree (life sciences/healthcare field is a plus), or an equivalent combination of education, training, and experience that presents the required knowledge, skills, and abilities; Previous experience working with healthcare; Experience with data analysis, Knowledge of Good Clinical Practice, local laws and applicable regulations in the region is a plus; Full working proficiency in English and Spanish; Portuguese is a plus; Excellent written and oral communication skills, as well as time management skills.

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