Clinical Program Scientist I

About Sarah Cannon Research Institute

Sarah Cannon Research Institute (SCRI), a subsidiary of McKesson, is among the largest community-based oncology research organizations. With a focus on advancing cancer treatments, SCRI has contributed to pivotal cancer therapy approvals and operates clinical trials at over 200 locations across the U.S. The organization is committed to transforming cancer care through clinical excellence and innovative research.

Mission

At SCRI, patients affected by cancer guide every decision. By uniting leading medical experts with compassionate caregivers, the institute personalizes treatment and advances the fight against cancer globally.

Role Overview

The Clinical Program Scientist (CPS) position supports SCRI Research Programs by providing scientific, administrative, and operational assistance to directors. This role is instrumental in advancing program goals through disease-specific knowledge and collaborative execution of projects.

Key Responsibilities

• Establish and nurture effective relationships within relevant organizational areas.
• Conduct disease program meetings under Associate Director supervision as needed.
• Attend and assist in Physician Program Director one-on-one meetings when required.
• Use tracking tools to identify study gaps and monitor protocol amendments impacting patient eligibility and treatment schedules.
• Collaborate with clinical associates to prepare and review accurate study summary updates.
• Create and present slide decks for internal stakeholders.
• Support evaluation and start-up activities for new studies, including organizing executive committee meetings, preparing agendas and materials, completing evaluation templates, and engaging with cross-functional teams.
• Maintain documentation of decisions from Leads Meetings at various levels and participate in sponsor or CRO meetings.
• Provide scientific assistance for Investigator-Initiated Trials, RFPs, and Accelero trials in partnership with personalized medicine teams.
• Develop expertise in relevant therapeutic areas, perform literature searches, and support marketing requests.
• Maintain program dashboards and assist with communication efforts such as study-specific and FDA approval emails.
• Conduct special projects as needed to support research programs.
• Adhere strictly to SCRI's Code of Conduct and complete all assigned training by designated deadlines.

Required Qualifications

• PhD strongly preferred.
• Minimum of 5 years in scientific roles within clinical research.
• Experience in oncology and clinical trial phases I through IV.
• Ability to source scientific literature supporting research projects.
• Commitment to gaining disease-specific and drug development expertise relevant to SCRI programs.
• Capacity to collaborate within diverse, cross-functional teams.
• Excellent organizational, communication, and time management abilities.
• Adaptability to dynamic environments and changing program needs.
• Resourcefulness and problem-solving skills.

Additional Information

This is a U.S.-based remote role with preference for candidates near Nashville, TN, or able to commute weekly to the Nashville office. Relocation assistance and visa sponsorship are not provided. SCRI emphasizes diversity and equal employment opportunities without discrimination.

Applicants should be mindful of fraudulent recruiting scams using McKesson's name; official communications will not request money or use unverified email sources.

Compensation and Benefits

The role offers a competitive salary package determined by skill, experience, performance, and market factors. Additional compensation may include bonuses and long-term incentives. Comprehensive benefits support employees' physical, mental, and financial health.