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 â€“ those who work to prevent it, fight it, and survive it â€“ 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 y our 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 r esponsible 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 record s 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 r esponsible 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 Director and Regional Site Manager of all study specific medical issues for guidance

You should have:

Knowledge of federal regulations, good clinical practices (GCP)
Knowledge of medical and research terminology
Computer skills including use of clinical trial database, electronic data capture, and MS Word or Excel
Excellent Verbal and written communication skills
Excellent interpersonal skills
The ability to communicate and work effectively with a diverse team of professionals
Organizational and prioritizing capabilities
The ability to work independently in a fast pace environment with minimal supervision at off-site facilities
At least one year of experience as a Clinical Research Coordinator or Study Coordinator

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 750 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 today. SCRI's research network brings together more than 1,300 physicians who are actively enrolling patients into clinical trials at more than 250 locations in 24 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.

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.

We are an equal opportunity employer and value diversity at our company. We do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status.

Sarah Cannon Research Institute

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Clinical Research Coordinator