Clinical Research Coordinator

Elevate Your Career - Join Our Mission

At Sarah Cannon Research Institute (SCRI), part of McKesson, we believe our team is our greatest asset. If you are passionate about making a difference in the fight against cancer and want to contribute to innovative oncology treatments, this is the opportunity for you. Join us in our mission to transform care for cancer patients globally.

Our Commitment

Every decision we make is centered around individuals battling cancer – those dedicated to prevention, treatment, and survival. By uniting top medical professionals with passionate caregivers, we are revolutionizing cancer treatment through clinical excellence and breakthrough research.

As a Clinical Research Coordinator, you will play a vital role in managing administrative and clinical tasks within our research clinics.

• Perform EKGs and assist in collecting necessary questionnaires.

• Facilitate the transport of lab collection supplies and support research staff in accessing patient research charts for data collection.

• Prepare research charts in advance of patient visits by ensuring all source documents, lab orders, and informed consent forms are current.

• Manage phone communications and gather data for real-time collection as needed.

• Assist research staff in timely completion of research documents.

• Maintain sufficient stock of office supplies and equipment across research clinics.

• Coordinate meetings, appointments, and schedules for the research program.

• Track and assist research staff in obtaining necessary training certifications.

• Prioritize queries based on their urgency and importance.

• Facilitate document signature collection, including adverse event and RECIST logs.

• Handle faxing and scanning of documents as required.

• Manage study correspondence and communication effectively.

• Participate in educational programs and complete required protocol training for studies.

Required Qualifications:

• High School Diploma (GED); vocational/technical training preferred.

• Experience in performing EKGs is a plus.

• Administrative experience in a healthcare setting is preferred.

• Certification as a Medical Assistant is beneficial.

• IATA certification for lab specimen shipping is preferred.

• Completion of spill kit training for hazardous materials is required.

We are eager to receive your application by November 14, 2025. Please ensure that your submission includes all necessary materials as outlined in the posting.

About Sarah Cannon Research Institute

SCRI stands as a global leader in oncology research, facilitating community-based clinical trials to enhance patient therapies over the past three decades. In partnership with US Oncology Research, we are advancing clinical trial access nationwide, with over 750 first-in-human trials and significant contributions to recent FDA-approved cancer therapies. Our research network collaborates with more than 1,300 physicians across 250+ locations in 24 states. Join us in redefining cancer care.

We care deeply about the health and well-being of our patients and communities, starting with our dedication to our employees. Our comprehensive Total Rewards package supports the physical, mental, and financial health of our diverse workforce.

As part of our Total Rewards, we offer a competitive compensation package based on performance, experience, skills, and market evaluations. Additional compensation options may include bonuses and long-term incentives.

At SCRI, we embrace diversity and equality. We are proud to be an equal opportunity employer and do not discriminate based on race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status.