MCRA is the leading global full-service medical device, diagnostics, and biologics CRO and consulting advisory firm. MCRA delivers to its client’s industry experience, integrating its six business value creators: regulatory, clinical research, reimbursement, healthcare compliance, quality assurance, and distribution logistics to provide a dynamic, market-leading effort from innovation conception to commercialization. MCRA’s integrated application of these key value-creating initiatives provides unparalleled value for its clients. MCRA has offices in Washington, DC, Hartford, CT, New York, NY, and Tokyo, Japan and serves nearly 1,000 clients globally. Its core focus areas of therapeutic experience include orthopedics, spine, biologics, cardiovascular, diagnostic imaging, wound care, artificial intelligence, dental, anesthesia, general surgery, digital health, neurology, robotics, oncology, general and plastic surgery, urology, and in vitro diagnostic (IVD) devices and medical device cybersecurity. MCRA places particular emphasis on its expertise working with companies in all stages of development and throughout the technology life cycle by ushering technologies from the conceptual pre-clinical stage to market approval.
Clinical Affairs • Quality Assurance • Regulatory Affairs • Reimbursement • Healthcare Compliance
51 - 200 employees
November 15
51 - 200
Seeking a Director of Regulatory Review Programs for a non-profit client, responsible for FDA submission oversight and compliance.
September 10
51 - 200
MCRA seeks Director, Cardiovascular Regulatory Affairs for cardiac device regulatory strategy.
June 28
51 - 200
April 27
51 - 200