My client, a large International CRO are looking for experienced CRA's to join their team in Germany. This is working on behalf of an industry leading company, with projects available across a variety of therapeutic areas.
If you are an experienced CRA with a minimum of 1 years experience and are looking for a company where you can expediate your development, my client offers the perfect working environment to do just that due to the strong management team in place in Germany.
1 years independent monitoring experience, preferably in a CRO setting • Fluent in German (minimum C1 level) • Ability to perform 6-8 visits per month nationwide
Perform site qualification, initiation, routine monitoring, and site closure activities with a focus on data integrity, patient safety, and protocol compliance. • Develop and maintain strong relationships with investigative sites, ensuring effective communication and collaboration throughout the duration of the study. • Review and verify clinical data, source documents, and study records to ensure accuracy, completeness, and compliance with applicable regulations. • Proactively identify and resolve study-related issues and discrepancies, escalating as necessary to ensure timely resolution and adherence to project timelines. • Provide support and guidance to junior team members, including training, mentoring, and oversight as needed.