Clinical Research Coordinator

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 a Clinical Research Coordinator your primary responsibility is to screen, enroll and follow study subjects, ensuring protocol compliance and close monitoring while the subjects are on study. You are responsible for all data collection, source documentation, completing study specific case report forms, and submission of adverse experience reports. 

• You will support enrolling patients onto clinical trials through recruitment, screening, enrollment and follow up of eligible subjects according to protocol requirements  

• You will be responsible for working with the principal investigator to meet or exceed study enrollment.  

• You will review the study design and inclusion/exclusion criteria with physician and patient  

• You will ensure the protection of study patients by verifying informed consent procedures and adhering to protocol requirements/compliance  

• You will ensure the integrity of the data submitted on Case Report Forms or other data collection tools by careful source document review; monitors data for missing or implausible data  

• You will ensure that adequate and accurate records are maintained for inspecting 

• You will create study specific tools for source documentation when not provided by sponsor  

• You will collect, complete, and enter data into study specific case report forms or electronic data capture systems as needed  

• You will generate and track drug shipments, device shipments, and supplies as needed  

• You will report and follow up on serious adverse events as necessary  

• You will implement study-specific communications  

• You will ensure timely adherence to protocol requirements  

• You will be responsible for completion of all required documentation according to site working practice guidelines  

• You will ensure timely and accurate data completion  

• You will maintain accurate and complete records including regulatory documents when applicable, signed informed consent forms, source documentation, drug dispensing logs, device utilization logs, subject logs and study-related communications  

• You will track and report adverse events, serious adverse events, protocol waivers, deviations, and violations  

• You will communicate all protocol-related issues to appropriate study colleagues or manager  

• You will attend study specific on site meetings, investigator meetings, conference calls and monthly CRC meetings as required or asked to do so  

• You will apprise the principal investigator, Research Operations <