Clinical Research Associate (JS)

Founded in 1981, Atrium is a privately held healthcare products company located in Hudson, NH. Atrium manufactures over 2,000,000 sterile medical products each year which are distributed to over 60 countries either direct or through various international distribution partners and/or OEM customers. Maintaining a commitment to innovation in research, market development and manufacturing has enabled the company to excel in many global medical device markets.  With twenty-five years of experience, Atrium has been an innovator of new technologies designed to meet the clinical needs of the vascular patient, developing the latest advances in interventional vascular technologies. Whether it is drug delivery, drug coated stents, or new ways to deal with vascular disease, Atrium is working on a new and innovative ways to solve unmet clinical needs.

 

This would be an outstanding career opportunity!  Atrium's Clinical Research Group is rapidly expanding; offering unique opportunities for the experienced candidates with clinical research and monitoring experience.  If you're looking for a new challenge, working with a team of dedicated professionals, and can be available for up to 50%  travel; contact us to explore these exciting opportunities

Position Specific Requirements:Travel to clinical sites, nationally and internationally, to supervise and coordinate clinical studies.  Routine travel requirements (could be up to 50% mostly domestic travel).Monitor clinical studies and coordinate clinical activities to ensure compliance with protocol and overall clinical objectives. Oversee the conduct of all clinical studies to ensure the quality and integrity of data. Analyze and evaluate clinical data from the clinical sites to endure completeness and accuracy. Coordinate and resolve all quiries and problems associated with the clinical investigations. Assist in the preparation of clinical reports as needed for regulatory submissions and when requested for presentations, monographs and publications. Participate in the development of clinical standard operating procedures and clinical guidelines.

 

Qualifications:



BS, RN or equivalent with a minimum of 2 years experience site monitoring experience as a clinical research associate. CRA Certification is preferred.

Knowledge of FDA/TPP regulatory requirements preferred.  Attention to detail and good follow-through skills. Knowledge of the clinical development process and good guidelines for clinical practices. Strong interpersonal skills. Outstanding oral and written communication skills. Possess an understanding of scientific terminology and surgical practices. Medical device experience a plus!



Atrium Medical Corporation offers competitive salaries, exceptional benefits, and a business casual dress code. We do not accept unsolicited Agency Resumes. Atrium Medical Corporation is an equal opportunity employer dedicated to workforce diversity and a drug and smoke-free environment. Drug screening is required.