Study Lead I
McKesson, Nashville, TN, United States
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 that advance oncology treatments and improve outcomes for cancer patients worldwide. We look for mission‑driven candidates who are eager to fight cancer and make a difference in patients’ lives each day.
Our Mission
People who live with cancer—and 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, we transform care and personalize treatment. Through clinical excellence and cutting‑edge research, SCRI is redefining cancer care around the world.
Key Responsibilities
Support essential education and training to sponsors/CRO via kickoff calls or emails, delivering capability presentations and addressing client questions and concerns.
Participate in clinical operational reviews and attend site calls to evaluate study opportunities.
Conduct comprehensive feasibility assessments for clinical study leads using internal data and personnel as resources.
Collaborate with cross‑functional teams to gather necessary data and information for feasibility analysis.
Maintain a tracking system for the study lead life cycle.
Perform additional duties as assigned.
Mandatory
Adhere to SCRI’s Code of Conduct and Mission and Value Statement.
Complete required training assignments by their due dates.
Minimum Qualifications
Bachelor’s Degree.
At least 4 years of relevant experience.
At least 1 year of trial management experience.
Knowledge of the pharmaceutical industry, regulatory process, clinical trials, and medical terminology.
Strong attention to detail, execution, and ability to meet aggressive timelines; excellent interpersonal and communication skills.
Documented training in FDA regulations, GCP, and ICH guidelines for clinical trials.
Effective collaboration with internal and external partners, including investigators and site staff, using negotiation skills.
Proficiency in Microsoft Excel, Word, PowerPoint, and Outlook.
Ability to work within established timelines in a fast‑paced environment.
Preferred Qualifications
2 + years of trial management experience.
Certification in Clinical Research from ACRP or SOCRA.
Benefits
Our Total Rewards package includes comprehensive benefits to support physical, mental, and financial well‑being—such as competitive pay, bonus and long‑term incentive opportunities, and benefits through our parent company, McKesson. The package is designed to meet the diverse needs of our colleagues.
Applications are accepted through May 3, 2026.
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.
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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 that advance oncology treatments and improve outcomes for cancer patients worldwide. We look for mission‑driven candidates who are eager to fight cancer and make a difference in patients’ lives each day.
Our Mission
People who live with cancer—and 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, we transform care and personalize treatment. Through clinical excellence and cutting‑edge research, SCRI is redefining cancer care around the world.
Key Responsibilities
Support essential education and training to sponsors/CRO via kickoff calls or emails, delivering capability presentations and addressing client questions and concerns.
Participate in clinical operational reviews and attend site calls to evaluate study opportunities.
Conduct comprehensive feasibility assessments for clinical study leads using internal data and personnel as resources.
Collaborate with cross‑functional teams to gather necessary data and information for feasibility analysis.
Maintain a tracking system for the study lead life cycle.
Perform additional duties as assigned.
Mandatory
Adhere to SCRI’s Code of Conduct and Mission and Value Statement.
Complete required training assignments by their due dates.
Minimum Qualifications
Bachelor’s Degree.
At least 4 years of relevant experience.
At least 1 year of trial management experience.
Knowledge of the pharmaceutical industry, regulatory process, clinical trials, and medical terminology.
Strong attention to detail, execution, and ability to meet aggressive timelines; excellent interpersonal and communication skills.
Documented training in FDA regulations, GCP, and ICH guidelines for clinical trials.
Effective collaboration with internal and external partners, including investigators and site staff, using negotiation skills.
Proficiency in Microsoft Excel, Word, PowerPoint, and Outlook.
Ability to work within established timelines in a fast‑paced environment.
Preferred Qualifications
2 + years of trial management experience.
Certification in Clinical Research from ACRP or SOCRA.
Benefits
Our Total Rewards package includes comprehensive benefits to support physical, mental, and financial well‑being—such as competitive pay, bonus and long‑term incentive opportunities, and benefits through our parent company, McKesson. The package is designed to meet the diverse needs of our colleagues.
Applications are accepted through May 3, 2026.
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.
#J-18808-Ljbffr