Role Overview: We are looking for a motivated Clinical Research Associate (CRA) to join on a part-time contract basis (up to 0.8 FTE). The CRA will be responsible for monitoring clinical trial sites, ensuring compliance with study protocols, ICH-GCP guidelines, and local regulations. Key Responsibilities: Monitor clinical trial sites to ensure adherence to protocol and regulatory requirements Perform source data verification and ensure accurate reporting in eCRFs Oversee patient safety and adverse event reporting Assist with site initiation, routine monitoring visits, and study closeout Maintain effective communication with study teams, sponsors, and site staff Prepare and submit monitoring visit reports in a timely manner Support site training and troubleshooting as needed Qualifications: Bachelor’s degree in life sciences, pharmacy, nursing, or related field Minimum 3 - 5 years of CRA experience (CRO or pharma) Knowledge of ICH-GCP and local regulatory requirements Strong communication and organizational skills Willingness to travel to study sites within Germany What On Offer: Flexible contract arrangement (up to 0.8 FTE) Opportunity to work on innovative clinical trials Supportive and collaborative team environment Professional development opportunities Interested? Apply now for immediate consideration or contact Lloyd Broomes – LBroomes@planet-pharma.co.uk We are an equal opportunities Recruitment Business and Agency. We welcome applications from all suitably qualified candidates regardless of their race, sex, disability, religion/belief, sexual orientation or age. Planet Pharma is an Employment Business providing Global Staffing services.