Regulatory Coordinator 1, MCVI Research, FT, 8A-4:30P
Responsible for the regulatory aspects of the Division. This will involve preparation of paperwork for the Institutional Review Board, tracking of regulatory documents related to each protocol, and organization of documentation required by regulatory agencies (FDA,IRB.) Must be attentive to detail but able to work collaboratively in a high-volume, multi-tasked department to achieve goals. Excellent interpersonal skills and maturity are essential to deal with physicians, hospital departments as well as outside sponsors. Demonstrates effective time-management skills by prioritizing workload. Degrees: • High School Diploma or GED Additional Qualifications: • Individual with high level computer skills, legal and or clinical research background to work in intensive high volume regulatory environment. • College graduate preferred. • Must be detail oriented, very organized but able to multitask to handle high volume paperwork Essential: Excellent interpersonal skills/maturity required for both telephone and direct contact with customers, physicians and hospital personnel. • Must be able to work independently and efficiently without constant supervision to complete tasks by deadlines and contribute to the department goals as needed. • Must pursue and achieve certification in research after 2 years of working in the department. Minimum Required Experience: 2 years Apply tot his job