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JOB REQUIREMENTS: Help us change lives At Exact Sciences, we\'re helpingchange how the world prevents, detects and guides treatment for cancer. We give patients and clinicians the clarity needed to make confident decisions when they matter most. Join our team to find a purpose-driven career, an inclusive culture, and robust benefits to support your life while you\'re working to help others. Position Overview This position is responsible for assisting in the execution of clinical trials by providing quality administrative and project management support and contributing to documentation development. This position will coordinate with all members of the Clinical Affairs team and internal and external stakeholders to successfully execute the clinical study plans of the company. This position may be remote. Essential Duties Include, but are not limited to, the following: Contribute to clinical study protocol development by drafting/updating protocol synopsis and/or assisting with completion of protocol revisions, as requested. Assist with the development of or provide feedback on clinical study project plans, as requested. Contribute to development of regulatory documents (e.g., Annual Report). Provide project-specific systems administration support (e.g., SampleMinded). Collect essential documents and review for completeness and compliance with Standard Operating Procedures, the protocols and appropriate regulations; review Trial Master File (TMF) inventory for missing and expiring documents. Interact with clinical study sites to support study start-up, execution, and close-out activities. Create and maintain study related trackers, including but not limited to, enrollment, study supplies, receipt of samples, and site information. Coordinate the ordering, tracking, and accountability of clinical supplies, including investigational product materials, equipment, and special-order items as requested. Review for completeness and route legal documents for execution. File all versions in document management database. Draft study documents (study trackers, templates, presentations, etc.) as requested. Support case report form (CRF) development, participate in user acceptance testing (UAT) for electronic data systems and review related data management documents, as applicable. Represent Exact Sciences as a customer advocate/liaison both internally and externally. Coordinate study start-up, execution, and close-out activities, or... For full info follow application link. We are an equal employment opportunity employer. All qualified applicants will receive consideration for employment without regard to age, color, creed, disability, gender identity, national origin, protected veteran status, race, religion, sex, sexual orientation, and any other status protected by applicable local, state or federal law. Applicable portions of the Company\'s affirmative action program are available to any applicant or employee for inspection upon request. ***** APPLICATION INSTRUCTIONS: Apply Online: ipc.us/t/63C2D1B912894E73