Associate Clinical Trial Manager

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 will be part of the Clinical Affairs Team, which is responsible for planning, executing, managing, and closing projects associated with the company clinical study plans. The Associate Clinical Trial Manager manages, executes, and reports on clinical study operations; and provides support to members of the multidisciplinary project team, internally and externally. The Associate Clinical Trial Manager may work in conjunction with and/or with direction from a Clinical Trial Manager. Essential Duties include but are not limited to the following: Act as a customer advocate throughout the project lifecycle. Understand and support global project goals including site recruitment, patient recruitment, marketing, and PR, as appropriate. Implement approved clinical study protocols. Develops study-specific consent forms, and other trial related materials (e.g., Study Monitoring Plan, Patient Guide, Project Plan, etc.) as required. Coordinate with applicable cross-functional teams (e.g., R & D, Operations, Exact Sciences Laboratories) to identify goals and scope of clinical study projects; Manage and execute the overall project scope and timelines. Initiate and train sites to the study protocol; ensure proper site adherence to clinical research regulations. Manage resources and timelines associated with all study start-up and implementation activities, including CRO/investigator agreements, central IRBs, and contractual agreements. Support the management and oversight of CROs and other clinical study related vendors as applicable. Plans for and manages all materials to support the appropriate execution of the clinical projects, including but not limited to distribution of documents, forms, supplies, equipment, and investigational device. Ensure maintenance of document standardization through the use of model documents, templates and appropriate peer review. Ensure the appropriate development of all documents by CROs including but not limited to study documents, including informed consent forms, case report forms and instructions,... 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/E4E305333C4D4829