Clinical Research Coordinator B/C (Abramson Cancer Center)

Job Description

The Abramson Cancer Center (ACC) of the University of Pennsylvania is a world leader in developing and conducting innovative clinical trials for the prevention, diagnosis, and treatment of cancer. The mission of the ACC Clinical Research Unit (CRU) is to advance the science of cancer care, serve our patients by improving clinical outcomes, and offer the best available innovative care to trial participants.

The Clinical and Translational Research Program for Lymphomas and Other Related Diseases ("Lymphoma Research Team") within the ACC CRU seeks a full-time Clinical Research Coordinator B/C (CRC).

Clinical Research Coordinator B Responsibilities:

• Plan, organize, and contribute to study-related meetings...
• Assist with start-up processes for Industry-sponsored, Cooperative Group, and Investigator-initiated studies...
• Assist the Regulatory Coordinator by preparing components of submissions...
• Lead or contribute to Informed Consent in accordance with federal and Pennsylvania state law...
• Provide support to faculty and staff during study-related visits...
• Collect, review and report timely, valid, and accurate data...
• Coordinate independent central review of clinical trial end-points...
• Maintain complete, well-organized, and audit-ready study and participant files...
• Participate in research meetings and Sponsor/CRO teleconferences...
• Perform other duties as reasonably assigned.

Clinical Research Coordinator C Responsibilities:

• Plan, organize, and run study-related meetings...
• Take a lead role in Site Feasibility and Qualification Visits...
• Prepare components of submissions to the IRB...
• Participate in the development of study-specific Case Report Forms...
• Participate in Sponsor teleconferences, Program meetings, and working groups...
• Assist the Unit Managers with QA processes related to research studies...

Position may involve some work-related responsibilities that may occur outside of usual hours and some conference-related travel. Position is contingent on continued funding.

Qualifications:

Clinical Research Coordinator B: Bachelor of Science and 2 to 3 years of experience or equivalent combination of education and experience is required.

Clinical Research Coordinator C: Bachelor of Science and 4 to 6 years of experience or equivalent combination of education and experience is required.