Proven experience as a Clinical Research Associate (CRA) or equivalent role.
Strong organizational, communication, and report-writing skills.
Fluency in English; additional language skills (e.g. german) advantageous.
Clinical Research Associate (CRA)
Location: Germany (Remote )
We are seeking a highly motivated Clinical Research Associate (CRA) to support multiple clinical studies. The Contractor will perform monitoring and site management activities while ensuring patient safety, regulatory compliance, and high-quality data in accordance with applicable SOPs, study protocols, and ISO 14155:2020.
Perform remote monitoring and interim site management as required., Support site start-up activities including EC/CA submissions/amendments, contract negotiation, and documentation preparation/collection., Report non-compliance of investigators with their Clinical Study Agreements (CSAs) to the Client., Support audit preparation and responses., Perform additional services or projects only upon written approval from the Client.]