Clinical Research Coordinator

As the Clinical Research Coordinator you are responsible for overall clinical operations of the facility’s research program including enrollment, regulatory, quality, and site operations.

You will support enrolling patients onto clinical trials through recruitment, screening, enrollment, treatment, and follow-up of eligible participants according to protocol requirements.

You will review the study design and inclusion/exclusion criteria with physicians and patients

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

You will collect, complete, and enter data into study specific case report forms (CRFs) or electronic data capture systems within study required timelines

You will ensure the integrity of the data submitted on case report forms or other data collection tools by careful source document review and monitoring data for missing or implausible data

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

You will generate and track drug shipments, lab kits, and other supplies

You will be responsible for accurate and complete documentation of protocol requirements according to site work instructions and standard operating procedures (SOPs)

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

You will maintain accurate and complete records, including regulatory documents, signed informed consent forms, source documentation, drug dispensing logs, screening and enrollment logs, and study communications

You will coordinate regular site research meetings

You will attend study-specific on-site meetings/visits, investigator meetings, conference calls, and other coordinator meetings, as required and you will work closely with monitors, study teams and site staff to ensure quality study data

You will communicate site status through a weekly activity report to appropriate site/management colleagues

You should have:

An Associate’s Degree, preferably a Bachelor’s Degree

Knowledge of medical and research terminology

Knowledge of FDA Code of Federal Regulations and GCP

Knowledge of the clinical research processes

Public presentation skills

The ability to manage multiple ongoing priorities and projects with a diverse team of professionals

About Sarah Cannon Research Institute

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. In 2022, SCRI formed a joint venture with former US Oncology Research to expand clinical trial access across the country. 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 enrolling patients into clinical trials at more than 200 locations in 20+ states across the U.S. Please click here to learn more about our research offerings.

We care about the well-being of the patients and communities we serve, and that starts with caring for our people. That’s why we have a Total Rewards package that includes comprehensive benefits to support physical, mental, and financial well-being. Our Total Rewards offerings serve the different needs of our diverse colleague population and ensure they are the healthiest versions of themselves. For more information regarding benefits through our parent company, McKesson, please click here.

As part of Total Rewards, we are proud to offer a competitive compensation package. This is determined by several factors, including performance, experience and skills, equity, regular job market evaluations, and geographical markets. In addition to base pay, other compensation, such as an annual bonus or long-term incentive opportunities may be offered.

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