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; perform data entry; resolve data queries with Sponsor or 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.
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. Effective communication, writing skills and problem solving capabilities are necessary. Must have the ability to multitask and to work as part of a team or independently. Knowledge of IRB and human research protection regulations preferred.
Reference Number: 40-25010
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