Biospecimen Coordinator
University Overview
The University of Pennsylvania, the largest private employer in Philadelphia, is a world-renowned leader in education, research, and innovation. This historic, Ivy League school consistently ranks among the top 10 universities in the annual U.S. News & World Report survey. Penn has 12 highly-regarded schools that provide opportunities for undergraduate, graduate and continuing education, all influenced by Penn's distinctive interdisciplinary approach to scholarship and learning.
Job Description Summary
The Tara Miller Melanoma Center (TMMC) within Penn Medicine's Abramson Cancer Center unites research, education, outreach, and patient care programs to drive advances in melanoma and other skin cancer diagnosis, prognosis, and treatment. The Biospecimen Coordinator will play an integral role in the TMMC's research program. The incumbent will be responsible for the coordination of biospecimens for several translational research projects and our biospecimen repository.
Job Responsibilities
Patient Accrual & Enrollment
- screen provider's clinic schedules for new study participants, verify eligibility, and circulate emails to providers for potential study participants to consent
- conduct informed consent
- enroll patients into PennChart and PennCRMS database assist with screening patients for potential clinical trials or studies.
Biospecimen Collection
- schedule biospecimen collections, coordinating with collaborating research labs and cores, and clinical staff
- prepare and drop off biospecimen collection kits
- coordinate the distribution of biospecimens to collaborating research labs
- record biospecimen collections & distributions into databases, oversee biospecimen supply inventory.
Project Management
- screen patients for eligibility to enroll into projects
- routinely update study calendars and project databases
- draft progress reports on ongoing projects
- participate in the development/maintenance of data collection tools
Regulatory & Compliance
- organize, participate, and assist in the preparation of regulatory documentation required for the IRB, CTRSMC, and other regulatory bodies
- assist with preparing documents for protocol modifications, audits, and annual continuing review
- assist with establishing and maintaining SOPs
Other duties as assigned. Position is contingent upon funding.
Qualifications
- Bachelor of Science and 1 to 2 years of experience or equivalent combination of education and experience is required.
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