Study Site Manager Bam (biospecimen Management & Acquisition)(m/f/d)
Roche UK
United Kingdom
Clinical trial management
Regulatory compliance (ivdr, gcp)
Etmf and documentation management
At Roche, you can show up as yourself, embraced for the unique qualities you bring
Job Summary
At Roche, you can show up as yourself, embraced for the unique qualities you bring.
In this role, you will be responsible for the design, planning, and coordination of analytical performance studies at study centers.
As part of the BAM Study Management & Sample Data Team within Research & Development, you will play a key role in shaping the future of diagnostic innovations.
Matching Summary
At Roche, you can show up as yourself, embraced for the unique qualities you bring.
Skills & Requirements
Must-have
Clinical trial management
Regulatory compliance (IVDR, GCP)
eTMF and documentation management
Study site monitoring and validation
Cross-functional collaboration
Nice-to-have
Open dialogue and genuine connections
Personal expression and acceptance
Thrive personally and professionally
Empowering each other to explore
Key Requirements
Minimum 3 years clinical research experience
Scientific degree (Bachelor, Master or equivalent)