Clinical Research Associate

About the Role

An internationally recognized Contract Research Organization (CRO) based in Germany is seeking knowledgeable Clinical Research Associates (CRAs) to join their team. This role involves contributing to clinical projects spanning diverse therapeutic fields with a company that fosters professional growth supported by a competent management team.

Key Responsibilities

• Perform site initiation, regular monitoring, and close-out visits aligned with clinical study protocols, regulatory mandates, and established SOPs.
• Execute site qualification, initiation, routine monitoring, and closure activities prioritizing data accuracy, patient safety, and adherence to protocols.
• Build and sustain effective partnerships with clinical sites to ensure smooth communication and cooperation during study conduct.
• Review and cross-verify clinical trial data, source documentation, and records for precision, thoroughness, and regulatory compliance.
• Proactively identify and address study-related challenges, escalating concerns as necessary to maintain timelines.
• Contribute to drafting and evaluating study documents such as protocols, informed consent forms, case report forms, and manuals.
• Offer mentorship and training to junior colleagues, providing guidance and oversight when appropriate.

Requirements

• At least 12 months of independent monitoring experience preferably acquired within a CRO environment.
• Proficiency in German at a minimum C1 level.
• Capability to conduct 5 to 7 site visits per month across Germany.

Additional Information

This position is based onsite in Germany and offers the opportunity to rapidly advance your career in clinical research.