Site Identification Specialist

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.