Sarah Cannon Research Institute · 2 days ago
Study Activation Coordinator - Remote US
Sarah Cannon Research Institute (SCRI) is a leading oncology research organization focusing on community-based clinical trials. The Study Activation Coordinator will support the Study Activation team by managing meeting agendas, recording minutes, and assisting with site processes to facilitate trial activation.
Research
Responsibilities
Maintain and update a database of potential pharmaceutical and CRO partnerships
Track and report site metrics related to activation processes for each Strategic Site
Prepare, update, and distribute meeting agendas, reports, and other relevant documentation
Assist with system maintenance, including uploading study documents and creating study folders within applicable platforms
Maintain internal reference materials to ensure alignment with strategic site processes
Collaborate with Strategic Sites to document and request required study access and supplies necessary for trial activation
Other duties as assigned
Qualification
Required
High School Diploma required
1+ year work experience in a fast-paced environment with healthcare, research, or pharmaceutical industries preferred
Knowledge of the pharmaceutical industry, regulatory processes, clinical trials and/or medical terminology
Work experience with MS Office products including Excel as well as solid organizational skills, computer skills, and communication skills
Preferred
Associate's or Bachelor's Degree preferred
Benefits
Comprehensive benefits to support physical, mental, and financial well-being
Competitive compensation package
Annual bonus or long-term incentive opportunities
Company
Sarah Cannon Research Institute
Sarah Cannon Research Institute is one of the world’s leading oncology research organizations conducting community-based clinical trials.
Funding
Current Stage
Late StageRecent News
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