Clinical Program Scientist

The Clinical Program Scientist (CPS) role will provide disease-focused, scientific, administrative, and overall support to the Associate Director and/or Director in the support of a SCRI Research Program(s).

• Builds and maintains working relationships across the organization relevant to the role
• Leads Program Review Committee (PRC) meetings in support of a disease-specific program
• Attends and supports Physician Program Leader 1:1 meetings
• Tracks and maintains internal document of site capabilities
• Tracks and maintains document detailing site study gaps
• Awareness of protocol amendments and changes which affect patient eligibility/IP/treatment
• Collaborates with associate on one-page study summary updates
• Responsible for slide deck creation for internal teleconferences
• Tracks Physician Leaders pharmaceutical/community engagement activities
• Provides new study evaluation and start-up support

• PhD strongly preferred
• 5+ years working in a scientific capacity within clinical research
• Oncology experience and clinical research (phase I – IV) experience required
• Ability to pull scientific literature to support research projects
• Willingness to develop disease-specific and drug development expertise required
• 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 resourceful

• 401k matching
• Health insurance
• Flight privileges
• Total Rewards package

Sarah Cannon Research Institute (SCRI) is one of the world’s leading oncology research organizations conducting community-based clinical trials.