Clinical Research Associate

Overview My client, a large International CRO, is looking for experienced CRAs 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. Qualifications 1 year independent monitoring experience, preferably in a CRO setting Fluent in German (minimum C1 level) Ability to perform 6-8 visits per month nationwide Responsibilities Conduct site initiation, monitoring, and close-out visits in accordance with study protocols, regulatory requirements, and standard operating procedures (SOPs). 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. Assist in the development and review of study-related documents, including protocols, informed consent forms, case report forms, and study manuals. Provide support and guidance to junior team members, including training, mentoring, and oversight as needed. How to apply If you meet the criteria above, please apply via the following link or reach out directly at View email address on click.appcast.io #J-18808-Ljbffr