Support clinical and scientific studies, Collect, document, and control scientific data, Prepare monitor visits with paper-based and electronic systems, Ensure quality (e.g., check completeness of test documentation), Communicate with sponsors, Coordinate administrative matters for study management, Maintain investigator site files, Prepare documents for authorities and ethics committees, Assist with patient examinations, including lumbar punctures and intrathecal injections as well as blood draws, and prepare ECGs, Take, process, and ship biological samples, Serve as a contact person for patients, colleagues and contract research organizations, Participate in investigator and study meetings (via telephone or video conferences, attendance events at home and abroad)