Clinical Research Associate – Neurology, Oncology

This is a fully remote position, open to applicants in Germany.

📋 Description

• Oversee site qualification, initiation, interim monitoring, site management, and study close-out visits.

• Record findings from site visits through comprehensive written reports.

• Evaluate, supervise, and provide training to study site personnel on adherence to protocols as needed.

• Examine study subject safety information and ensure informed consent processes are properly followed.

• Perform source document verification to ascertain compliance, patient safety, and accuracy of data.

• Review Case Report Forms (CRFs) using both paper and electronic data capture systems, assisting sites with data query resolutions.

• Supply relevant updates for site-related documentation to be filed in the Trial Master File (TMF).

• Guarantee site compliance with the receipt, accountability, and return or destruction of investigational products (IP).

• Conduct accompanied site visits for the evaluation or training of other Clinical Research Associates (CRAs) as requested and when appropriate.

⛳️ Requirements

• Minimum of 2 years of experience as a Clinical Research Associate.

• Bachelor’s degree or RN/BSN in Nursing.

• Required experience in Neurology, Oncology, and Hematology.

• Willingness to travel as necessary.

• Exceptional interpersonal, verbal, and written communication skills in English.

• Outstanding organizational abilities with a keen attention to detail.

• Capability to work independently with minimal supervision.

• Proficient in Microsoft Office, Clinical Trial Management Systems (CTMS), and Electronic Data Capture (EDC) Systems.

🏝️ Benefits

• Supportive and collaborative team environment.

• Mentorship and guidance provided to less experienced staff.