Principal Scientist, Bmd Study Coordinator And Bmd Study Expert (bsc/bse) Biomarkers
Stellen Nordrhein Westfalen
Not specified
Biomarker outsourcing
Scientific biomarker monitoring
Vendor management
The job posting is for a Principal Scientist specializing in Biomarker Study Coordination at Stellen Nordrhein Westfalen, focusing on clinical operations and biomarker management. The ideal candidate should have significant experience in clinical trials, biomarker analysis, and project management, complemented by a relevant advanced degree
Job Summary
The Laboratory Excellence and Operation (LEO) and Biomarker Science and Operation (BSO) team provides key global resources for clinical trial teams focusing on biomarkers, including outsourcing, monitoring, vendor management, logistics, and sample coordination.
This role involves independently providing end-to-end operational support for clinical studies, focusing on biomarkers and PK samples, including study setup, sample tracking, assay and vendor setup, and study closure.
Key responsibilities include serving as a Biomarker Study Expert (BSE) and clinical team representative, partnering with clinical teams to set up and monitor biomarker/PK sample flow, and managing assay and sample management issues.
Matching Summary
Match Score: 85
The job posting is for a Principal Scientist specializing in Biomarker Study Coordination at Stellen Nordrhein Westfalen, focusing on clinical operations and biomarker management. The ideal candidate should have significant experience in clinical trials, biomarker analysis, and project management, complemented by a relevant advanced degree.
Skills & Requirements
Must-have
Biomarker outsourcing
Scientific biomarker monitoring
Vendor management
Biomarker logistics
Clinical site communication
Sample coordination
End-to-end operational support
Nice-to-have
Proactive planning
Problem solving
Influencing skills
Curious mindset
Detail-oriented
Key Requirements
5+ years of clinical operations/bioanalysis/biomarkers experience
Advanced degree with 3 years in clinical operations/bioanalysis/biomarkers
M.Sc. in Life Sciences (or equivalent)
Fluent in English
Operational knowledge of clinical trials
Knowledge of regulatory requirements (ICH/GCP, GLP)