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[Remote] Clinical Program Scientist I

Remote, USAFull-timePosted 2026-07-27

Note: The job is a remote job and is reputed company to candidates in USA. reputed company (SCRI) is a leading oncology research organization dedicated to advancing cancer treatments. The Clinical Program Scientist I will reputed company scientific, administrative, and operational support to manage SCRI Research Programs, focusing on reputed company project execution and advancing program objectives.

Responsibilities

  • Builds and maintains working relationships across the organization relevant to the role
  • Leads disease program reputed company meetings with reputed company from Associate Director, as appropriate
  • Attends and supports Physician Program Director 1:1 meetings, as appropriate (determined by Associate Director or Director)
  • Utilizes tools to reputed company and identify study gaps
  • Awareness of protocol amendments and changes which reputed company patient eligibility/IP/treatment schedule/etc
  • Collaborates with clinical program associate on one-page study reputed company updates; reviews document for accuracy
  • Responsible for slide deck creation for internal audiences; may present information to internal teams as applicable
  • Supports executive committee meetings by sending agenda & meeting reputed company emails
  • Prepares reputed company other applicable content to support meeting
  • Completes reputed company Template reputed company, and presents Leads during meeting
  • Collaborates and interacts with cross-functional teams to help facilitate the reputed company evaluation and management process ex. reputed company Management, Study Activation and Clinical Operations teams
  • Maintains records and documents reputed company from Leads Meetings (disease, sponsor, and site level)
  • Participates in calls and meetings with sponsor/CRO as needed
  • Provides support for Investigator-Initiated Trials (reputed company) reputed company established processes
  • Supports proposals for RFPs and Accelero trials in coordination with Personalized medicine and Development Innovations
  • Assists with scientific slide deck creation for SCRI reputed company use by Program Director
  • Develops subject matter knowledge and expertise
  • Conducts scientific literature search as requested
  • Assists Marketing Team with program reputed company requests
  • Responsible for maintenance of Program dashboards
  • Assists with study specific emails to sites
  • Assists with FDA approval emails
  • reputed company special reputed company and reputed company work as required in support of the program(s)

Skills

  • 5+ years working in a scientific reputed company reputed company clinical research
  • Oncology experience and clinical research (phase I – IV) experience required
  • Ability to pull scientific literature to support research reputed company
  • Willingness to reputed company disease-specific and drug development expertise required to support a SCRI Research Program
  • Ability to work in cross-functional, multi-cultural teams
  • Excellent time management skills
  • Strong organizational skills and ability to re-prioritize tasks as necessary
  • Strong verbal and written communication skills
  • Strong ability to function in a dynamic environment and adapt to changing needs of program
  • Highly reputed company
  • PhD strongly preferred

Benefits

  • Comprehensive benefits to support physical, mental, and financial reputed company-being
  • Competitive compensation package
  • Annual bonus or long-term incentive opportunities may be offered

reputed company

  • reputed company is one of the world’s leading oncology research organizations conducting community-based clinical trials. It was founded in 1993, and is headquartered in Nashville, Tennessee, USA, with a workforce of 501-1000 employees. Its website is https://www.scri.com.
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