Consultant, Clinical Project Lead, Medical Devices

Employment Type

: Full-Time


: Miscellaneous

Our client, a global medical device manufacturer, has engaged GForce Life Sciences to identify a Clinical Project Lead who will be responsible for various aspects of assigned clinical studies, from protocol drafting through study summary and final report.

Duties / Expectations:
Draft clinical study protocols and prepare all technical reports, abstracts, and presentations required for assigned studies
Upon completion of an assigned study, compile a final report and summary of study results
Interpret and present study findings to colleagues, including members of the leadership team
Review relevant medical & scientific literature, study results, and data to stay up-to-date with trends in laboratory medicine
Identify necessary testing to address clinical risks for product changes
Provide consultation, from a clinical standpoint, for HEOR studies, HFE studies, and post market studies
Ensure safety, efficacy, and clinical utility of the assigned product

Mandatory Requirements:Bachelor of Science in Biology, Biochemistry, or related field
1-3 years of clinical laboratory or clinical research experience is required, with medical device experience being highly preferred
Must have experience drafting clinical study protocols
Demonstrated knowledge of technical writing and clinical study design
Knowledge of laboratory workflow related to blood collection and handling

Nice to Have Requirements:
Advanced degree in a health-related field
MT (ASCP) or equivalent is desirable
Project management experience
Previous experience working on clinical trials
IVD experience is a plus

Term & Start:
Start ASAP
12 + month contract 
Must be in Northeastern New Jersey or willing to relocate.

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