Sarah Cannon Research Institute (SCRI) is one of the world’s leading oncology research organizations, conducting community-based clinical trials. Focused on advancing therapies for patients over the last three decades, SCRI is a leader in drug development. It has conducted more than 850 first-in-human clinical trials since its inception and contributed to pivotal research that has led to the majority of new cancer therapies approved by the FDA in the past decade. SCRI’s research network brings together more than 1,300 physicians who are actively enrolling patients into clinical trials at over 200 locations in more than 20 states across the U.S.
Open Positions
Manager of Research Blood Cancer
A Bachelor’s Degree and knowledge of FDA guidelines and GCP required. Oncology experience preferred
Director Human Resources
10+ years of progressive HR experience, 5+ years in a senior HRBP or HR leadership role, Demonstrated experience managing complex employee relations issues independently
Tissue Coordinator
High school diploma or equivalent, 1-2 years of experience, valid driver’s license
Medical Assistant Oncology Research
Medical Assistant training and experience in a clinical setting, with skills in venipuncture and blood processing. Current BLS certification required
Clinical Trial Central Screener
3+ years of experience in clinical research and experience in clinical trials, with a bachelor's degree in nursing or a licensed registered nurse
Enrollment Research Nurse
Associate degree in Nursing, 1+ years of clinical nursing experience, and 1+ years of experience treating oncology patients
Lead Systems Engineer
10+ years of experience in systems engineering, a bachelor's or master's degree in a relevant field, and proficiency in system design tools and methodologies
Research Nurse
RN License, Associate Degree, at least one year of oncology experience, and research certification preferred
Laboratory Processing Technician
Vocational training or certification in laboratory science and/or phlebotomy. Current BLS certification. At least one year of clinical laboratory and phlebotomy or equivalent experience
Director, Portfolio Management
7+ years of experience in clinical research or project management, including prior people leadership, and minimum 2 years of experience in an Associate Director or equivalent role managing multiple complex clinical studies concurrently
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