CLINICAL RESEARCH COORD B
Duties: The Clinical Research Coordinator will be responsible for set-up, implementation, and oversight of research studies including managing and conducting recruitment, screening, enrollment and follow-up visits for all study participants. Oversees the day-to-day activities on the study website for multiple studies. Responsible for providing training and oversight to research staff. Coordinates and oversees all IRB correspondence, preparation and submissions of IRB amendments and closeout visits. Conduct and oversee adverse event reporting and follows good clinical practices for conducting human subjects research. Functions independently in carrying out most responsibilities. Meets with PIs regularly to provide study updates and for technical advice.
Qualifications: A Bachelor's Degree and 2 to 4 years of experience or equivalent combination of education and experience required. Excellent communication, interpersonal and organizational skills. Understanding of regulatory compliance issues preferred. Experience working with electronic systems and data systems, and understanding good data management practices preferred. Ability to work effectively both independently and as part of a team. Familiarity with MS Office Suite is essential.
Reference Number: 40-25815
Salary Grade: 026
Employment Type: Exempt
Org: ME-Division of Health Policy
Special Requirements: Background check required after a conditional job offer is made. Consideration of the background check will be tailored to the requirements of the job.
Job Family: I-Technical/Professional Research