[Remote] Clinical Program Scientist I

Note: The job is a remote job and is open to candidates in USA. Sarah Cannon Research Institute (SCRI) is a leading oncology research organization focused on advancing cancer treatments. The Clinical Program Scientist I will provide scientific, administrative, and operational support to the management of SCRI Research Programs, contributing to the advancement of oncology research and clinical trials.

Responsibilities

• Builds and maintains working relationships across the organization relevant to the role
• Leads disease program related meetings with oversight 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 track and identify study gaps
• Awareness of protocol amendments and changes which affect patient eligibility/IP/treatment schedule/etc
• Collaborates with clinical program associate on one-page study summary 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 summary emails
• Prepares all other applicable content to support meeting
• Completes Lead Template grid, and presents Leads during meeting
• 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 records and documents decisions from Leads Meetings (disease, sponsor, and site level)
• Participates in calls and meetings with sponsor/CRO as needed
• Provides support for Investigator-Initiated Trials (IITs) via 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 related use by Program Director
• Develops subject matter knowledge and expertise
• Conducts scientific literature search as requested
• Assists Marketing Team with program related requests
• 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 required in support of the program(s)

Skills

• 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

Benefits

• We care about the well-being of the patients and communities we serve, and that starts with caring for our people. That’s why we have a Total Rewards package that includes comprehensive benefits to support physical, mental, and financial well-being.
• Our Total Rewards offerings serve the different needs of our diverse colleague population and ensure they are the healthiest versions of themselves.
• For more information regarding benefits through our parent company, McKesson, please click here (https://www.mckesson.com/Careers/Employee-Benefits/).
• As part of Total Rewards, we are proud to offer a competitive compensation package.
• This is determined by several factors, including performance, experience and skills, equity, regular job market evaluations, and geographical markets.
• In addition to base pay, other compensation, such as an annual bonus or long-term incentive opportunities may be offered.

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