CLINICAL RESEARCH COORD A
Duties: The Clinical Research Coordinator A will assist in the coordination of Phase I-IV clinical trials, including coordination, organization, and maintenance of all documentation required by Sponsor or CRO; data entry; resolve data queries with Sponsor of CRO; recruit, screen and enroll potential study subjects from inpatient, outpatient and emergency room; participate in the conduct of audits; process and ship blood, stool and specimens; schedule patient visits and any necessary testing; obtain records required to complete case report forms; conduct initiation, monitoring and closeout visits with Sponsor or CRO; adhere to all Penn ICF and FDA guidelines; prepare and process all IRB documentation. Weekend work may be required as specified in protocols.
Qualifications: A Bachelor's Degree and 1 year to 3 years of experience or equivalent combination of education and experience required. Effective problem solving capabilities as well as effective communication and writing skills. Ability to multitask and demonstrated ability to work as part of a team or independently. Knowledge of IRB and human research protection regulations preferred.
Reference Number: 40-28754
Salary Grade: 025
Employment Type: Exempt
Job Family: I-Technical/Professional Research