Responsibilities
- Manages central laboratory and specialty vendors across a mix of variably complex clinical trials
- Manages acquisition of clinical trial samples
- Provides support for sample related matters to clinical study teams
- Works with ICF Specialist and wider team to ensure compliance with ICF permissions
- Assists with vendor selection and oversight
- Provides input to clinical trial related documents under the supervision of the Lead
- Executes biomarker plans in collaboration with the study team and Lead
- Prepares request for proposals, reviews and assess bids and Statement of Work (SOW)
- Performs other duties as necessary to ensure optimal clinical trial execution
Requirements
- Minimum of 6 years relevant industry experience
- Science background and working knowledge of a wide array of medical terms, biological assays including proteomics, cellular assays and genomics
- Understanding of bioethics of human biospecimen collection and research
Nice to Have
- Oncology experience
Work Arrangement
Remote (Worldwide)
Additional Information
- 100% homebased position
- Dedicated to one of our key global sponsors
