Clinical Research Coordinator

McKesson; United States; On-site; USD 79,000 - 90,000; Full time

Job summary

Sarah Cannon Research Institute (SCRI) is seeking a Clinical Research Coordinator for Blood Cancer and Bone Marrow Transplant trials. You will manage enrollment, regulatory compliance, data entry, and site operations to ensure high-quality trial conduct.

You will review study designs with physicians, protect patient rights, coordinate shipments, and monitor safety events while collaborating with monitors, investigators, and staff across multiple sites.

Qualifications

• Associate's degree required; Bachelor's preferred.
• Knowledge of medical and research terminology.
• Knowledge of FDA Code of Federal Regulations (CFR) and Good Clinical Practice (GCP).
• Clinical research processes knowledge.
• Public presentation skills.
• Ability to manage multiple priorities with a diverse team.
• At least one year of oncology experience, preferably hematology/oncology and/or transplant.
• At least one year of clinical research setting experience.
• At least one year of experience managing blood cancer and/or BMT trials preferred.
• Research certification (ACRP or CCRP) preferred.
• RN or LPN preferred.

Responsibilities

• Oversee enrollment, regulatory, quality, and site operations for blood cancer and BMT research.
• Support enrollment onto clinical trials through recruitment, screening, and follow-up per protocol.
• Review study design and inclusion/exclusion criteria with physicians and patients.
• Ensure informed consent procedures and protocol adherence for patient protection.
• Enter data into CRFs or electronic data capture systems within required timelines.
• Maintain data integrity through source document verification and data monitoring.
• Create study-specific source documentation tools when not provided by sponsor.
• Coordinate drug shipments, lab kits, and other supplies.
• Document protocol requirements per SOPs and work instructions.
• Track and report adverse events and deviations.
• Maintain regulatory documents and study communications.
• Organize regular site research meetings and attend required visits and investigator meetings.
• Provide weekly activity reports to site/management.

Skills

Oncology experience

Clinical research

Public presentation skills

Multitasking

Regulatory knowledge

Education

Associate's Degree

Bachelor's Degree preferred

ACRP/CCRP certification

Job description

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.

Clinical Research Coordinator Responsibilities

As the Clinical Research Coordinator for Blood Cancer and Bone Marrow Transplant (BMT) research you are responsible for overall clinical operations of the facility's blood cancer 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.
• At least one year of oncology experience, preferably in hematology/oncology and/or transplant.
• At least one year of experience in a clinical research setting.
• At least one year of experience managing blood cancer and/or BMT clinical trials is preferred.
• Research certification (ACRP or CCRP) is preferred.
• RN or LPN is preferred.

Salary range $79,000 - $90,000

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.

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 reg