Clinical Program Scientist I

General tasks in the support of a SCRI Research Program(s). Tasks can include but may not be limited to:

• Builds and maintains working relationships across the organization relevant to the role

• Leads disease program related meetingswith oversight from Associate Director as appropriate

• Attends and supports Physician ProgramDirector1:1 meetings as appropriate (determined by Associate Director or Director)

• Utilizes tools to track and identify study gaps

• Awareness of protocol amendments and changes which affect patient eligibility/IP/treatment schedule/etc.

• Collaborates withclinical programassociate on one-page study summary updates; reviews document for accuracy

• Responsible for slide deck creation for internalaudiences; may present information to internal teams as applicable

Provides new study evaluation and start-up support. Tasks can include but may not be limited to:

• Supportsexecutive committeemeetings by sending agenda & meeting summary emails

• Prepares all other applicable content to support meeting

• CompletesLead Templategrid and presentsLeads duringmeeting;

• Collaborates and interacts with cross-functional teams to help facilitate the lead evaluation and management process ex. Lead Management Study Activation and Clinical Operations teams

• Maintains recordsanddocuments decisions from Leads Meetings (disease sponsor and site level)

• Participates in callsand meetingswith sponsor/CRO as needed

Provides scientific support for a SCRI Research Program(s). Includes but may not be limited to:

• Provides support for Investigator-Initiated Trials (IITs)via established processes

• Supports proposals for RFPs andAccelerotrialsin coordination withPersonalized medicine and Development Innovations

• Assists with scientific slide deck creationfor SCRI related useby Program Director

• Develops subject matter knowledge and expertise

• Conducts scientific literature search as requested

• Assists Marketing Teamwith program related requests

Provides materials in support of a SCRI Research Program(s). Includes but may not be limited to:

• Responsible for maintenance of Program dashboards

• Assists with study specific emails to sites

• Assists with FDA approval emails

• Perform special projects and related work as requiredin support of the program(s).

Mandatory:The following are mandatory expectations of all SCRIemployees.

• Practices and adheres to the Code of Conduct philosophy and Mission and Value Statement.

• During your employment with SCRIyou will be routinely assigned training requirements. You are expected to complete any training assignments by the due date.

Qualifications:

• 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 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 resourceful

This is a remote position based in the United States. Preference will be given to candidates located in the Nashville TN area or those able to commute to our Nashville home office one day per week. Relocation and visa sponsorship are not available.

Interested candidates should submit their application through Applications will be accepted through July 31st 2026. Please ensure all required materials are included as outlined in the posting.