Clinical Research Coordinator

McKesson’s Corporate; Nashville (TN); On-site; USD 60,000 - 75,000; Full time

Benefits offered by this job

Total Rewards package

Job summary

Sarah Cannon Research Institute (SCRI) is seeking a Clinical Research Coordinator to manage clinical operations for the facility’s research program, including enrollment, regulatory, quality, and site operations. You will support enrolling patients onto trials through recruitment, screening, enrollment, treatment, and follow-up per protocol.

You will review study designs with physicians, ensure informed consent, and maintain accurate regulatory and data documentation across CRFs or EDC systems,

Qualifications

• Knowledge of medical and research terminology
• Knowledge of FDA Code of Federal Regulations and GCP
• Knowledge of the clinical research processes
• Public presentation skills
• Ability to manage multiple priorities with a diverse team

Responsibilities

• Oversee enrollment, regulatory, quality, and site operations of the research program.
• Support enrolling patients onto clinical trials through recruitment, screening, enrollment, treatment and follow-up.
• Review study design and inclusion/exclusion criteria with physicians and patients.
• Verify informed consent procedures and adherence to protocol requirements.

Skills

Medical terminology

GCP knowledge

Regulatory knowledge

Multitasking

Public presentation

Education

Associate’s Degree

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.

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 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‑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.

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‑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.

About McKesson

We deliver careers with purpose and potential. Our focus on better health starts with creating an inclusive environment with strong values where you can build a fulfilling career. You can count on us to provide you with resources and opportunities to grow and be your best, while contributing to our pursuit of improving lives.

Every day, McKesson’s employees deliver products to healthcare providers that make a difference in the care and life of a patient. We work to distribute medical supplies, bandages, syringes, vials of flu vaccine, and pharmaceutical drugs to help real patients like Jack, an eight-year-old boy battling cancer.

We take that job seriously. Together, the work we do is shaping the future of healthcare.

If you are passionate about combining a meaningful career with a balanced life, join us on this journey and apply for a job with McKesson today.

Every day, McKesson’s employees deliver products to healthcare providers that make a difference in the care and life of a patient.