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.