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 Job #02953 Email this job to a friend
About our client
Our client has developed many of the most innovative lifesaving devices, techniques and therapies used in cardiology and vascular medicine today.
Position Location
Senior Clinical Research Associate Connecticut
Salary
Highly competitive package, commensurate with experience
Responsibilities
1) Conduct site visits and monitor clinical studies
2) Coordinate clinical activities to ensure compliance with protocol and overall clinical objectives
3) Assist with protocol development and project oversight of single and multi-center clinical studies
4) Prepare protocols, Investigator’s brochures, CRFs, ICFs and other specialized documents
5) Propose and negotiate budgets for clinical investigations
6) Analyze and evaluate data from clinical sites to ensure completeness as well as accuracy
7) Prepare clinical reports (as needed) for regulatory submissions and for presentations, monographs and publications
8) Follow and participate in the ongoing development of departmental clinical SOPs as well as clinical guidelines
Requirements
1) Advanced degree preferred
2) 3 – 5 years of clinical monitoring experience
3) Familiarity with managing staff in foreign offices, particularly India

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