Medical Device firm on the northshore is seeking a Senior Clinical Research Associate to design
and conduct pre-market clinical trials in support of regulatory marketing applications, as well
as post-market clinical studies and surveys in support of marketed products.
Reporting to the Manager of Clinical Research, this individual will coordinate all aspects of
clinical studies for this company's devices to include developing, writing and implementing
protocols and all associated study documents. Other responsibilities include participating in
the pre-release evaluation process for new products prior to commercialization, and also
providing clinical support to cross-functional teams during product development cycles.
Ideal candidates have a minimum of 3 years experience in medical device industry, clinical
setting or research field. An understanding of domestic and international product approval
process is required. .
Only 20% travel, paying 75K+ depending on experience.
Must have a bachelor's degree in a scientific discipline and knowledge of Good Clinical
Practices (GCP's), Quality Systems Regulation (QSR), and HIPAA requirements.