Senior Clinical Trial Manager

EXACT SCIENCES CORPORATION • Madison, WI • 8h ago

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 The Senior Clinical Trial Manager (CTM) is responsible for
supporting or leading the management, planning, execution, and closure
of clinical studies. The Sr. CTM works collaboratively and
cross-functionally in an exciting, fast paced environment to oversee the
day-to-day operations of assigned clinical studies and ensure the
successful execution of the company\'s clinical research plans. This
position may be remote. Essential Duties Include, but are not limited
to, the following: Coordinate and oversee the operational aspects of a
study including planning, start-up, enrollment and close out activities
ensuring that deliverables are completed on time, within budget, and in
compliance with department procedures, applicable regulations and
quality standards. Prepare, review and implement study related plans and
documents including project timelines, study protocols, informed consent
forms (ICFs), recruitment plans, monitoring plans, study budgets, site
contracts & budgets, vendor management plans and other essential
clinical study documents. Develop plans for systems and materials
required to support the efficient execution of clinical studies and is
responsible for effective management during the conduct of the study.
Develop, implement and maintain tools to manage, monitor and report on
study health & operations, project timelines, and study finances to
department management and other stakeholders. Participate in study
database development by reviewing and contributing to case report form
(CRF) design, CRF completion guideline development, edit check & manual
data review requirements, and participation in user acceptance testing
(UAT). Oversee sample management activities including planning, sample
handling, kit supply management, sample shipping, processing, and
resulting. Develop site recruitment plans and is responsible for the
identification, selection, start-up and performance monitoring of
clinical research sites. Develop study budgets and is responsible for
accurately forecasting and managing study expenses. Oversee site... 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/CCCE7C56592D4495

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