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MCRA, an IQVIA business, is a premier medical device advisory firm and clinical research organization (CRO) that excels in integrating regulatory, clinical research, reimbursement, healthcare compliance, and quality assurance services. With a strong commitment to delivering exceptional value, MCRA supports clients throughout the entire lifecycle of medical device development, from concept to commercialization. The firm boasts a global presence with offices in Washington, DC, Manchester, CT, and New York, NY, as well as operations in Japan and Europe, serving over 1500 clients worldwide. MCRA specializes in various therapeutic areas, including orthopedics, spine, cardiovascular, neurology, digital health, diagnostic imaging, wound care, dental, general healthcare, robotics, and in vitro diagnostic (IVD) devices.
MCRA
The Director, Clinical Affairs will oversee clinical trials and ensure compliance with regulatory requirements while supporting the CRO leadership team.
MCRA
MCRA is seeking a Clinical Research Associate to manage investigator sites and monitor clinical studies in compliance with regulatory standards.
MCRA
MCRA is seeking a Senior Clinical Research Associate to manage investigator sites and monitoring activities in compliance with GCP guidelines.
MCRA
MCRA is seeking a Clinical Research Associate to manage investigator sites and monitor clinical studies.
MCRA
MCRA is seeking a Director of Cardiovascular Regulatory Affairs to manage regulatory submissions and strategy for cardiac Interventional clientele.
MCRA
MCRA is seeking top talent for its general application talent pool for future job openings.
MCRA
MCRA is looking for an Associate Director/Director to lead regulatory strategy and submissions for cardiac electrophysiology clients.
MCRA
The Associate, Clinical Contracts and Budgets will support the negotiation of clinical trial agreements and site budgets for clients engaged in clinical research.
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