About this role
Job title: Clinical Research Associate - Neurology, Oncology - Germany
About the Role Join Worldwide Clinical Trials as a Clinical Research Associate focused on Neurology and Oncology in Germany. You will collaborate with diverse therapeutic teams and receive extensive support in regulatory submissions, TMF management, and onsite mentoring for sites across multiple studies.
What You'll Do
- Responsible for site qualification, initiation, interim monitoring, site management, and study close-out visits.
- Provide mentoring and guidance to less experienced CRAs and site staff when needed.
- Document site visit findings via written reports.
- Assess, monitor, and train study site staff on protocol adherence as required.
- Review study subject safety information and informed consent.
- Conduct source document verification for compliance, patient safety, and veracity of data.
- Review CRFs using paper or electronic data capture systems and assist sites with data query resolution.
- Provide applicable updates for site related documentation for filing in the Trial Master File (TMF).
- Ensure site compliance with IP receipt, accountability and return or destruction.
- Conduct accompanied site visits for assessment or training of other CRAs as requested and appropriate.
What We're Looking For
- Excellent interpersonal, oral, and written communication skills in English.
- Superior organizational skills with attention to detail.
- Ability to work with little or no supervision.
- Proficiency in Microsoft Office, CTMS and EDC systems.
- 2+ years of experience as a Clinical Research Associate.
- 4-year university degree or RN/BSN in Nursing.
- Experience in Neurology, Oncology and Hematology is required.
- Willingness to travel required.