Clinical Program Associate

McKesson’s Corporate; Northern (KY); On-site; USD 65,000 - 95,000; Full time

Job summary

Sarah Cannon Research Institute (SCRI), a McKesson subsidiary, seeks a Clinical Program Associate to provide administrative support to a SCRI Research Program. The role partners with a Clinical Program Scientist and Director to advance disease-specific initiatives and enrollment efforts.

The candidate will track enrollment, prepare study summaries, draft emails, and coordinate cross-functional activities across sites. A bachelor's degree and 3+ years in oncology or clinical research are required.

Qualifications

• Bachelor's degree required and 3+ years of oncology or clinical research experience.
• Broad oncology or clinical research knowledge (phase I–IV).
• Strong verbal and written communication, prioritization, and cross-functional collaboration.

Responsibilities

• Track enrollment and update study documents across SCRI programs.
• Coordinate protocol amendments and study summaries for sites.
• Draft disease KOL lists and distribute program materials.
• Support interdepartmental actions across multiple teams for at-risk studies.

Skills

Verbal communication

Written communication

Prioritization

Cross-functional teamwork

Adaptability

Education

Bachelor's degree

Job description

## Clinical Program AssociateApplyremote type: Fully Remotelocations: USA, TN, Remotetime type: Full timeposted on: Posted Yesterdayjob requisition id: JR0152401**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.Therapeutic Development provides centralized oversight of all projects which encompass a SCRI Research Program. These projects result in the execution of disease-specific and organizational research goals. The Clinical Program Associate role will provide administrative and overall support to a Clinical Program Scientist, and/or Associate Director, and/or Director in the support of a SCRI Research Program(s).**Duties and Responsibilities:***General tasks in the support of a SCRI Research Program(s). Tasks can include but may not be limited to:** Tracks enrollment and updates relevant documents* Tracks study cohorts* Tracks protocol amendments* Creates and updates one page study summaries; circulates to appropriate sites with oversight* In partnership with Disease Program Team, drafts and maintains list of disease KOLs by region/expertise/etc.* Drafts study summary emails for sites; drafts program-specific material for distribution* Distributes Therapeutic Development supported materials to network* Supervise and forward questions to appropriate stakeholders from shared department mailbox* Ad-hoc projects and related work as required* Tracks and maintains actions for Therapeutic Development team initiatives* Coordinate interventional actions across multiple teams for at risk studies* Supports partner enrollment targets that may be inclusive of diversity targets**Provides materials in support of a SCRI Research Program(s) with manager oversight, as appropriate. Includes but may not be limited to:*** Drafts Open to Enrollment (OTE) emails* One page summaries* Disease committee content* Drafts and sends FDA approval emails* Assists with slide deck creation**Mandatory: The following are mandatory expectations of all SCRI employees.*** Practices and adheres to the “Code of Conduct” philosophy and “Mission and Value Statement.”* During your employment with SCRI, you will be routinely assigned training requirements. You are expected to complete any training assignments by the due date.**Minimum Qualifications:*** Bachelor's Degree* 3+ years of relevant experience, preferably in oncology or clinical research* Broad oncology OR clinical research (phase I – IV) knowledge* Willingness to develop in-depth expertise required to support a SCRI Research Program* Ability to work in cross-functional, multi-cultural teams* Good verbal and written communication skills* Good prioritization skills* Strong ability to function in a dynamic environment and adapt to changing needs of program***This is a remote position based in the United States. Relocation and visa sponsorship are not available.****Interested candidates should submit their application through* *https://www.scri.com/careers/**. Applications will be accepted through August 24, 2026. Please ensure all required materials are included as outlined in the posting.***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-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.McKesson has become aware of online recruiting-related scams in which individuals who are not affiliated with or authorized by McKesson are using McKesson’s (or affiliated entities, like CoverMyMeds or RxCrossroads) name in fraudulent emails, job postings or social media messages. In light of these scams, please bear the following in mind: McKesson Talent Advisors will never solicit money or credit card information in connection with a McKesson job application.McKesson Talent Advisors do not communicate with candidates via online chatrooms or using email accounts such as Gmail or Hotmail. Note that McKesson does rely on a virtual assistant (Gia) for certain recruiting-related communications with candidates.McKesson job postings are posted on our career site: careers.mckesson.com.*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.*