CLINICAL RESEARCH COORD A
Duties: The Clinical Research Coordinator A duties will include the conduct of clinical trials, including screening, consenting and enrolling study subjects; preparation and submission of IRB documentation; scheduling patient visits and any necessary testing; attend investigator initiation meetings; obtain records to complete case report forms; conduct initiation, monitoring and closeout visits with Sponsor or CRO; data collection, both database and interview data; preparing figures and tables for inclusion in manuscripts.
Position is contingent on continued funding.
Qualifications: A Bachelor's Degree and 1 year to 2 years of experience or equivalent combination of education and experience is required.
The candidate should be experienced with Microsoft, Office, Excel and Powerpoint, as well as RedCap. The ideal candidate will have strong analytical ability, excellent interpersonal skills, flexibility, attention to detail, and comfort working independently. Comfort in a medical setting, handling confidential patient information and patient contact is essential. Knowledge of basic medical terminology and extraction of clinical data is preferred.
Reference Number: 40-25159
Salary Grade: 025
Employment Type: Exempt
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