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We are currently looking to fill a CMC (chemistry, manufacturing and controls) Regulatory Sciences Specialist. Regeneron successfully manufactures a r
The Temp Specialist, Site Contracts Lead is responsible for ensuring the delivery of high quality, compliant, effective, and timely work product and m
The Executive Director of Medical Affairs provides strategic leadership for the diabetic retinopathy program (Eylea) with high visibility in the organ
The Imaging Sciences group is the home of many brand-new imaging core facilities, including the Preclinical in vivo Imaging Center, Preclinical Histol
We are currently looking to fill a Lead Investigation Specialist position. This position performs all compliance related tasks vital to complete inves
Summary: Serves as Lead and also performs all tasks necessary for the manufacturing operations of both clinical and commercial manufacturing programs
Associate Biotech Production Specialist Regeneron successfully manufactures a range of biopharmaceuticals for patients worldwide, including our appro
Our client, a leading Pharmaceutical Company is hiring a Principal Veterinary Scientist on a contracting basis. Location: Lawrenceville NJ (remote ...
Piper Companies is looking for an Associate Director, Drug Product and Manufacturing for a growing biopharmaceutical company in Wilmington, DE. Res...
Piper Companies is currently seeking a Director of Clinical Operations to fill an opportunity with a growing and innovative Biopharmaceutical compa...
Piper Companies is currently seeking a Vice President of Medical Research to fill an opportunity with a growing and innovative Biopharmaceutical co...
Piper Clinical Solutions is currently seeking a motivated Clinical Data Manager in Bethesda, MD to support a Clinical Research Organization. You wi...
Piper Clinical Solutions is seeking a motivated Regulatory Affairs Specialist in Bethesda, MD to support an established research firm supporting bo...
Oversee, Prepare, and/or Review aggregate safety review documents (eg, DSUR, PBRER) and safety sections of relevant clinical trial documents.