We are a dynamic group of professionals providing regulatory, quality and clinical services for the medical device industry. Our team supports start-ups, mid-sized private companies and large corporations at all stages of the product life cycle. We work across a broad spectrum of technologies and treatment modalities; our clients develop both next generation and paradigm shifting devices. Our product exposure includes implantables, instruments (manual, laser, robotic, etc.), capital equipment, combination products, software as a medical device (SaMD), medical apps, in vitro diagnostics and more.
We are seeking an experienced Clinical Research Associate (CRA) to support our clinical operations team. The CRA will act as project resource to clinical site, sponsor, and Experien Group personnel regarding the product under test and the clinical trial conduct. The person will participate in the planning, development and execution of clinical trials to evaluate the safety, effectiveness and performance of medical devices. Under management supervision, CRAs monitor assigned clinical trials to ensure adherence to Federal regulations, clinical protocol, company policies, and any other applicable procedures.
MAJOR DUTIES OF POSITION:
KNOWLEDGE AND SKILL REQUIREMENTS:
The above description is intended to describe the general content, identify the essential functions of, and requirements for the performance of this job. It is not to be construed as an exhaustive statement of duties, responsibilities or requirements.
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