Sarah Cannon Research Institute-posted 3 days ago
Full-time • Entry Level
Remote
501-1,000 employees

It’s More Than a Career, It’s a Mission. Our people are the foundation of our success. By joining our growing team at Sarah Cannon Research Institute (SCRI), a subsidiary of McKesson, you will have the opportunity to become part of one of the largest community-based cancer programs to advance oncology treatments and improve outcomes for cancer patients across the globe. We look for mission-driven candidates who have a desire to advance the fight against cancer and make a difference in the lives of patients diagnosed with cancer every day. Our Mission People who live with cancer – those who work to prevent it, fight it, and survive it – are at the heart of every decision we make. Bringing the most innovative medical minds together with the most passionate caregivers in their communities, we are transforming care and personalizing treatment. Through clinical excellence and cutting-edge research, SCRI is redefining cancer care around the world. The Study Activation Coordinator is responsible for supporting the Study Activation team by preparing and distributing meeting agendas, recording minutes and action items, and assisting with site-facing processes. Additionally, this position is responsible for uploading study-related documents to designated systems utilized by SCRI and will serve as the primary point of contact for internal SC departments, Strategic Site physicians and staff, Contract Research Organizations (CROs) and pharmaceutical partners. This is a fully remote position based in the US; relocation assistance and visa sponsorship are not available for this role.

  • 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.
  • High School Diploma required, Associate's or Bachelor's Degree preferred
  • 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.
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