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As a Site Activation Specialist, you will serve as a Single Point of Contactto perform feasibility, site activation and some maintenance activities in assigned studies for investigative sites, according to applicable regulations, SOPs and work instructions, working closely with the Site Activation Manager, Project Management team, and other departments as necessary.

You will review documents for completeness, consistency, and accuracy, under guidance of senior staff and prepare site documents, inform team members of completion of regulatory contractual. 

Along with distributing completed documents to sites and internal project team member and updating and maintaining internal systems, databases, tracking tools, timelines, and project plans with accurate and complete project specific information.

You will also review, track, and follow up the progress, the approval and execution of required documents such as questionnaires, CDAs, regulatory, ethics, Informed Consent Form, and Investigator Packrelease documents. 

Requirements: 

• Bachelor’s Degree in Life Science or related field

• 2-4 years’ prior experience in Clinical Research organizations.

• Knowledge of German Language will be a plus

• Ability to work independently but also collaborate with others

• Good interpersonal, communication and organisational skills to establish and maintain effective working relationships with co-workers, managers and sponsors

• Ability to work on multiple projects

• Knowledge of applicable functional/regulatory requirements, including local regulations, SOPs and ICH/GCP