Clinical Research Associate

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 5-7 visits per month nationwide

• 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.