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Clinical Program Scientist

5+ years
Not Disclosed
10 April 25, 2025
Job Description
Job Type: Full Time Education: PhD Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Job Title: Clinical Program Scientist
Job ID: JR0129366
Location: Tennessee, Remote
Category: Medical Programs Specialist, Medical & Medical Research
Post Date: April 22, 2025


Job Description

Our Mission:
At Sarah Cannon Research Institute (SCRI), a subsidiary of McKesson, we are driven by a mission to advance oncology treatments and improve outcomes for cancer patients globally. Join our team, where your work will make a real difference in the fight against cancer. We are looking for mission-driven candidates who are passionate about advancing cancer research and care.

Role Overview: The Clinical Program Scientist (CPS) will provide scientific, administrative, and disease-focused support to the Associate Director and/or Director of a SCRI Research Program. This includes supporting disease-specific and organizational research goals, collaborating across teams, and ensuring the smooth execution of clinical projects.

Key Responsibilities:

  • Build and maintain relationships across the organization relevant to the role.

  • Lead Program Review Committee (PRC) meetings for disease-specific programs with oversight from the Associate Director, as appropriate.

  • Support Physician Program Leader meetings and maintain documents related to site capabilities, study gaps, and protocol amendments.

  • Collaborate with disease program teams to maintain a list of key opinion leaders (KOLs) and track engagement activities.

  • Create and present scientific and program-related slide decks for internal teleconferences and meetings.

  • Support new study evaluation and start-up, including organizing meetings, tracking decisions, and maintaining necessary records.

  • Provide scientific support for Investigator-Initiated Trials (IITs) and Clinical Development Plans (CDP), as directed.

  • Assist with the creation of scientific slide decks, including gathering relevant content.

  • Develop subject matter knowledge and expertise and conduct scientific literature searches as needed.

Qualifications:

  • Education: PhD strongly preferred.

  • Experience: 5+ years working in a scientific capacity within clinical research, with oncology experience required (phases I-IV).

  • Skills:

    • Ability to work cross-functionally in multi-disciplinary teams.

    • Strong time management and organizational skills.

    • Excellent verbal and written communication skills.

    • Ability to adapt to changing needs in a dynamic environment.

    • High resourcefulness and self-sufficiency.

Additional Information:

  • Location: Remote (Tennessee).

  • Benefits: Comprehensive benefits package, including physical, mental, and financial well-being support, along with competitive compensation.


About Sarah Cannon Research Institute (SCRI):
SCRI is a leader in community-based oncology research, with over 750 first-in-human clinical trials and a global impact on drug development. The organization collaborates with over 1,300 physicians across 250 locations to advance cancer care.

We are committed to creating a diverse and inclusive work environment and are an equal opportunity employer.