Clinical Research Associate

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.