Duties: The Clinical Research Coordinator A will participate in the coordination of Phase I-IV clinical trials, including recruitment, screening and enrollment of potential study participants; preparation of study budgets with partnering institutions and industry; coordination, organization, and maintenance of all documentation required by Sponsor or CRO; resolve data queries with Sponsor or CRO; process and ship blood and specimens; schedule patient visits and any necessary testing; obtain records 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 submit all IRB documentation.

Qualifications: A Bachelor's Degree and 1 year to 2 years of experience or equivalent combination of education and experience required. Effective problem solving capabilities, communication skills and writing skills are necessary. Ability to multitask and demonstrated ability to work as part of a team or independently is preferred. Working knowledge of IRB and human research protection regulations preferred.

Reference Number: 40-26461

Salary Grade: 025

Employment Type: Exempt

Org: DM-Gastroenterology

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

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