| Company profile |
| Founded in 1981, Atrium is a privately held healthcare products company located in Hudson, NH. Atrium is a market leading manufacturer of breakthrough medical device technologies used in open heart surgery, emergency chest trauma, thoracic drainage and surgical repair of diseased blood vessels. More recently, Atrium is known for its high technology presence in coronary stents, minimally invasive intervention of peripheral blood vessels, state-of-the-art hernia repair, drug delivery research, hemodialysis access, and market leadership in facial plastic surgery. Atrium manufactures over 1,000,000 sterile medical products each year which are distributed to over 60 countries. Maintaining a commitment to innovation in research, market development and manufacturing has enabled the company to excel in many global medical device markets. With more than two decades of experience, Atrium has been an innovator of new technologies designed to meet the clinical needs of the patient. Whether it is chest drainage, drug delivery, drug coated stents, or new ways to deal with vascular disease and general surgery, Atrium is working on a new and innovative ways to solve unmet clinical needs. Atrium offers a unique opportunity with exciting challenges for the qualified candidate. |
| Job details | |
| Job industry : | Biotechnology/Pharmaceutical |
| Job segment : | Education/Research |
| Job role : | Other |
| Job skill : | Clinical Research Associate |
| Position vacant : | Clinical Research Associate II JS |
| Job location : | Hudson, New Hampshire |
| Job code : | JS |
| Job details | |
| Company name : | Atrium Medical |
| Minimum experience : | 3 years |
| Maximum experience : | 5 years |
| Job type : | Permanent |
| Gross pay : | Negotiable for the right candidate |
| Job posted : | Jun 18, 2007 |
| Job description | |
| Job description: | CLINICAL RESEARCH ASSOCIATE II (JS)
Position Type Full Time Location Hudson, New Hampshire Date Posted 6/18/2007 Position Specific Requirements: Conduct site visits, monitor clinical studies and coordinate clinical activities to ensure compliance with protocol and overall clinical objectives. Assist with protocol development and project oversight of single and multicenter clinical studies. Prepare protocol,investigator's brochure, case report forms, informed consent and other specialized documents. Propose and negotiate budgets for clinical investigations. Analyze and evaluate data from clinical sites to ensure completeness and accuracy. Prepare clinical reports as needed for regulatory submissions and when requested for presentations, monographs and publications. Follow and participate in the ongoing development of departmental clinical standard operating procedures and clinical guidelines. Participate and assist in the planning and organization of investigator meetings or ad hoc clinical advisory meetings as required. Acquire and maintain professional, product and market expertise via independent reading, networking and training. Maintain current clinical knowledge base through familiarity with clinical literature and attendance and participate in project meetings and seminars. Ad hoc projects as assigned by manager and other duties that commensurate with associated training and experience. Develop potential applications to exploit new business opportunities. Qualifications: Bachelor degree or equivalent plus a minimum of two to five years experience as a Clinical Research Associate or monitor. Demonstrated knowledge and understanding of good clinical practices, the medical device development process and regulatory pathways for clinical trials. Strong interpersonal skills and the ability to interact with physicians in a professional manner. Possess an understanding of scientific terminology and medical and surgical practices. Outstanding oral and written communication skills. Attention to detail and good follow through skills. Medical device industry experience is strongly preferred. CRA Certification is a plus! Ability to travel. Travel requirements will vary *(up to 50%) depending on the status of current projects. 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. |
| How to apply : | Register to view |
| Third party mediation allowed : | No |
| Telecommute : | No |
| Travel required : | Up to 50% |
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