We're looking for a Laboratory Study Manager, working in the Biotechnology/Medical Devices industry in King of Prussia, Pennsylvania, United States.
Reviews and provides recommendations to study-related laboratory test components written in a study outline and/or protocol that are appropriate and necessary for the clinical hypothesis through dialogue with the Clinical Development Teams.
Reviews and provides laboratory expertise as a Subject Matter Expert on the set up, creation and logistics and technical support with a laboratory vendor for a given study.
Inputs and supports for the SETs should be related to GLP analytical tests, laboratory specifications, design of the kits, technical and operational data transfers and overall end to end process.
We are offering Competitive Compensation and Benefits. This position may present an opportunity to go permanent.
Our client is an award-winning clinical development company. Improving lives globally with 20+ years experience in clinical research and strategic resourcing. Elevating results with proven strategies, comprehensive solutions, and customized delivery models.
Serving pharmaceutical, biopharmaceutical, biotechnology, and medical device organizations.
Strong relationships provide you connections and access to great opportunities. Industry expertise sets you up for success with helpful insights, career coaching, and professional training. Grow and learn while you put your skills to work.
Experience Required for Your Success
Bachelor's degree or equivalent in Life Science, Nursing, Pharmacy, Medical laboratory technology or other health/medical related area preferred (Other degrees and laboratory certifications considered relevant to perform described job descriptions)
2 years laboratory experience is required
GLP experience is required
What Do You Think?
Does your experience reflect what it takes to be successful in this role? Do the work and challenges get you excited about what's possible? Apply here.