Clinical Research Assistant
McKessonAbout the role
It’s More Than a Career, It’s a Mission.
Our people are the foundation of our success. By joining our growing team at Sarah Cannon Research Institute (SCRI), a subsidiary of McKesson, you will have the opportunity to become part of one of the largest community-based cancer programs to advance oncology treatments and improve outcomes for cancer patients across the globe. We look for mission-driven candidates who have a desire to advance the fight against cancer and make a difference in the lives of patients diagnosed with cancer every day.
Our Mission
People who live with cancer – those who work to prevent it, fight it, and survive it – are at the heart of every decision we make. Bringing the most innovative medical minds together with the most passionate caregivers in their communities, we are transforming care and personalizing treatment. Through clinical excellence and cutting-edge research, SCRI is redefining cancer care around the world.
As the Clinical Research Assistant you will perform administrative and clinical duties at research clinics.
You will perform EKGs
You will assist with collection of required questionnaires
You will facilitate transport of lab collection supplies to designated areas for collection
You will support the research staff in locating patients’ research charts for patient visits and data collection
You will prepare research charts for upcoming visits by ensuring current source documents are on the chart, correct labs are ordered, and new version of informed consent forms (ICF) is printed
You will manage phone messages, collects data from existing records as needed for real time data collection
You will provide assistance to the research staff to ensure research documents are completed in a timely manner
You will ensure there is an adequate stock of office supplies and equipment for all research clinics
You will schedule and coordinates meetings, appointments and calendars for research program
You will track and assist in obtaining outstanding training for nurses and investigators as needed
You will assist in prioritizing queries based on due date and importance
You will facilitate obtaining signatures on necessary documents including but not limited to adverse event (AE) and RECIST logs
You will fax/scan documents as needed
You will send on/off study correspondence to appropriate persons
You will participate in educational programs and activities
You will attend required meetings You will complete protocol training for required studies
You should have for this position:
A High School Diploma (GED), Medical Vocational/Technical training is preferred
Experiencing performing EKGs is preferred
Administrative experience is preferred
Experience in healthcare is preferred
Certified Medical Assistant
IATA certified to assist clinics with shipping of lab specimens
Completion of spill kit training for cytotoxic agents and bio-hazardo
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