Sarah Cannon Research Institute
Study Activation Coordinator - Remote US
Sarah Cannon Research Institute, Nashville, Tennessee, United States
Study Activation Coordinator – Remote US
Sarah Cannon Research Institute
(SCRI), a subsidiary of McKesson, is seeking a mission‑driven candidate for this fully remote position based in the US. Relocation assistance and visa sponsorship are not available. 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 passionate caregivers, we are transforming care and personalizing treatment. Through clinical excellence and cutting‑edge research, SCRI is redefining cancer care around the world. Role Overview
Responsible for supporting the Study Activation team by preparing and distributing meeting agendas, recording minutes and action items, and assisting with site‑facing processes. Upload study‑related documents to designated systems and serve as primary point of contact for internal SC departments, Strategic Site physicians, CROs, and pharmaceutical partners. Duties
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. Qualifications
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. Experience with MS Office products including Excel; solid organizational, computer and communication skills. About Sarah Cannon Research Institute
SCRI is one of the world’s leading oncology research organizations, conducting community‑based clinical trials and advancing therapies for patients. Since 2022, SCRI has expanded clinical trial access across the country and has conducted more than 750 first‑in‑human clinical trials, contributing to pivotal research leading to new FDA‑approved cancer therapies. Benefits
We offer a competitive compensation package determined by performance, experience and skills, equity, regular market evaluations, and geographical markets. Base pay may include an annual bonus or long‑term incentive opportunities. The Total Rewards package includes comprehensive benefits to support physical, mental, and financial well‑being. Equal Opportunity Employer Statement
We are an equal opportunity employer and value diversity. We do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status.
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Sarah Cannon Research Institute
(SCRI), a subsidiary of McKesson, is seeking a mission‑driven candidate for this fully remote position based in the US. Relocation assistance and visa sponsorship are not available. 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 passionate caregivers, we are transforming care and personalizing treatment. Through clinical excellence and cutting‑edge research, SCRI is redefining cancer care around the world. Role Overview
Responsible for supporting the Study Activation team by preparing and distributing meeting agendas, recording minutes and action items, and assisting with site‑facing processes. Upload study‑related documents to designated systems and serve as primary point of contact for internal SC departments, Strategic Site physicians, CROs, and pharmaceutical partners. Duties
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. Qualifications
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. Experience with MS Office products including Excel; solid organizational, computer and communication skills. About Sarah Cannon Research Institute
SCRI is one of the world’s leading oncology research organizations, conducting community‑based clinical trials and advancing therapies for patients. Since 2022, SCRI has expanded clinical trial access across the country and has conducted more than 750 first‑in‑human clinical trials, contributing to pivotal research leading to new FDA‑approved cancer therapies. Benefits
We offer a competitive compensation package determined by performance, experience and skills, equity, regular market evaluations, and geographical markets. Base pay may include an annual bonus or long‑term incentive opportunities. The Total Rewards package includes comprehensive benefits to support physical, mental, and financial well‑being. Equal Opportunity Employer Statement
We are an equal opportunity employer and value diversity. We do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status.
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