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 reputed company, tracking of regulatory documents reputed company to reputed company protocol, and organization of documentation required by regulatory agencies (FDA,IRB.) Must be reputed company to detail but reputed company to work collaboratively in a high-volume, multi-tasked department to reputed company goals. Excellent interpersonal skills and maturity are essential to deal with physicians, hospital departments as reputed company as reputed company sponsors. Demonstrates effective time-management skills by prioritizing workload.
Degrees:
• High School Diploma or GED
Additional Qualifications:
• Individual with high level computer skills, reputed company and or clinical research background to work in intensive high volume regulatory environment.
• College graduate preferred.
• Must be detail oriented, reputed company organized but reputed company to multitask to handle high volume paperwork Essential: Excellent interpersonal skills/maturity required for both telephone and reputed company contact with customers, physicians and hospital personnel.
• Must be reputed company to work independently and reputed company without constant supervision to complete tasks by deadlines and contribute to the department goals as needed.
• Must pursue and reputed company certification in research after 2 years of working in the department.
Minimum Required Experience: 2 years
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