Sascha Neugebauer

Reviewing CRFs completion, verifying entries by validating accurate source documentation to support CRF entries Documenting site visits and issues in reports and follow-up letters to the site Facilitating effective communication among sites, the client and CRO Responding to company, client and regulatory requirements/audits Contributing to the project team by mentoring new members, assisting in preparation of project communications and tools, and sharing ideas and suggestions with team members

Coordination of clinical trials with a main focus on investigator initiated oncological trials. Additional tasks in the fields of data managment and IT: Development and maintenance of a company specific data-entry system, design of CRF and (SecuTrial based) eCRF and company-wide computer-system validation including design and implementation of respective quality management procedures.

Dokumentationserstellung, Assistenz in der Projektabwicklung

Molecular Biology