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Precision Medicine Group
Clinical Research Associate
Remote · Germany · Full time · Entry level
About the role
Monitor and manage clinical studies at investigative sites ensuring compliance with protocols and regulations. Coordinate study setup and ongoing monitoring activities.
What you’ll do
• Monitor clinical study progress at investigative sites. • Ensure studies follow protocol, SOPs, ICH-GCP, regulations. • Coordinate study setup activities including regulatory submissions. • Conduct pre-study and initiation visits. • Identify investigators and support study monitoring.
What you’ll bring
• Graduate or postgraduate in scientific or healthcare discipline. • At least 6 months CRA experience in CRO or pharma/biotech. • Excellent communication and organizational skills. • Fluency in English and German. • Availability for up to 60% domestic travel.
Life at Precision Medicine Group
High CRA retention rates and supportive management. Emphasis on work/life balance and employee voice.
About Precision Medicine Group
Precision Medicine Group is a precision medicine CRO specializing in oncology and rare diseases. They combine clinical trial design, operational expertise, and biomarker analytics to advance cancer therapies.