Sarah Cannon Research Institute · 12 hours ago
Manager of Research Processing Laboratory
Sarah Cannon Research Institute (SCRI) is a leading oncology research organization focused on advancing cancer treatments through community-based clinical trials. The Manager of the Processing Laboratory will oversee laboratory operations for oncology clinical trials, ensuring adherence to protocols, managing staff performance, and maintaining high-quality processing of specimens.
Research
Responsibilities
You will manage performance and professional development of the Processing Laboratory team
You will create, monitor, document and follow departmental SOPs, Work Instructions and corporate guidelines
You will ensure proper safety, operations and maintenance of laboratory equipment
You will educate and train staff on how to read and utilize laboratory manuals
You will oversee the high-level medical laboratory processing procedures of specimens received on patients enrolled in clinical trials
You will confirm inventory and evaluate the acquisition of study supplies and source documents necessary for obtaining pharmacology samples prior to patient treatment
You will ensure expert processing and shipping of bone marrow samples according to lab instructions provided by the study sponsor
You will ensure expert processing and shipping of pharmacokinetic/pharmacodynamic and all other samples according to instructions provided by the study sponsor
You will confirm accurate records, including freezer sample logs and sample acquisition and shipping
You will verify the scheduling of appropriate courier for sample shipments
You will ensure adequate supplies of dry ice are available for all shipments
You will assist staff with responding to queries generated from study sponsors or contract labs regarding patient/sample data
You will partner with Centennial Medical Center (CMC) Laboratory leadership as needed regarding labs for research patients
You will partner with Tennessee Oncology Laboratory leadership as needed regarding labs for research patients
You will lead the development of tools, processes and forms to enhance the efficiency and the quality of work in the Processing Laboratory
You will prepare reports for leadership, sponsors, CROs and other individuals/groups as needed
You will meet with investigators, study monitors, and others in coordinating study logistics; participate in staff meetings, site initiation and other meetings which will impact the delivery of quality research and compliance
You will receive and triage information requests; research and provide information where appropriate
Qualification
Required
A Bachelor Degree
The ability to read, understand, and comply with research protocols
Strong computer skills with demonstrated ability using clinical trial databases, electronic data capture, MS Access or Excel
Resourceful with heightened analytical abilities and problem solving skills in a fast paced environment
Excellent interpersonal skills, detailed-oriented and meticulous
Clinical and/or scientific experience in a research setting required
Management experience required
Preferred
Clinical and/or Scientific experience in a research setting specifically with working with profiling preferred
Research certification (ACRP or CCRP) preferred
Benefits
Comprehensive benefits to support physical, mental, and financial well-being
Competitive compensation package
Annual bonus or long-term incentive opportunities
Company
Sarah Cannon Research Institute
Sarah Cannon Research Institute is one of the world’s leading oncology research organizations conducting community-based clinical trials.
Funding
Current Stage
Late StageRecent News
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