The Client I have partnered with a fast growing biotech research and diagnostics company who are hiring a number of Scientific positions. They are based in West London.
The Role - Validate targeted proteomic, lipidomic and metabolomic assays to clinical standard (GCLP, CLIA etc)
- Independently applies scientific principles to achieve project objectives, including the design and execution of complex experiments, and analysis and interpretation of data under limited supervision
- Assessing viability and feasibility of new assays
- Execute project deliverables for biomarker studies in clinical trials by project scope of work and within sponsor-specific timelines
- Manage day-to-day operational aspects of clinical biomarker projects
- Assist in preparation and adherence to trial documents i.e., Project Protocols, Data Transmittal Forms etc
- Ensure project documentation are complete, current, and stored appropriately. Manage key documents/processes i.e., Project Management Plan, Communication Plan, Escalation Plan, Risk Management Plan, and appropriate Clinical Trial Management Systems (CTMS)
- Identification of scope out quests – working with appropriate team(s) to revise work orders to meet changing needs and requirements.
About You - PhD in biochemistry/related subject desirable
- 3+ years’ experience in mass spectrometry operation and method development
- Experience using Waters triple quadrupole machinery essential
- Quality Assurance/Compliance in clinical trials settings; Experience in Clinical trials/mass spectrometry in a clinical environment desirable
