• Clinical Affairs Associate

    Job Locations US-WI-Madison
    Req No.
    2018-2271
    Category
    Clinical Operations
    Type
    Regular Full-Time
  • Summary of Major Responsibilities

    This position is responsible for assisting in the execution of clinical trials by providing quality administrative and project management support. 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.

    Essential Duties and Responsibilities

    • 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.
    • Interacts 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 Investigator Meetings, as requested.
    • Responsible for completing assigned tasks to support study timelines and metrics with minimal ongoing direction.
    • Identify and report problems, investigate alternatives, and make recommendations for resolution and process improvements.
    • Responsible for organizing cross-functional project meetings. Distribute agendas, take and distribute meeting minutes.
    • Provide follow-up support and data collection for Research and Development teams to advance project objectives.
    • Initiate purchase requests, liaise with Accounts Payable and vendors as needed.
    • Provide support to Clinical Study Manager for clinical study budget review, tracking, and maintenance.
    • Must be able to work both independently and collaboratively as part of the clinical study team to meet study objectives and timelines.
    • Author and provide input to Clinical Affairs business processes.
    • Maintain a working understanding of current SOPs, work instructions, applicable regulations and guidance documents, such as FDA Code of Federal Regulations (CFR) and International Council on Harmonisation (ICH), Guideline for Good Clinical Practices (GCP).
    • Maintain applicable clinical study data in Clinical Trial Management System.

    Qualifications

    Mandatory Skills

    • General knowledge of applicable clinical research principles and requirements, including GCP and ICH guidelines.
    • Ability to organize, present, and convey problems or
    • Experience in using basic software applications including Microsoft Office (Word - generate documents and tables, Excel - create and modify spreadsheets, create complex formulas, ); Email – preferably Outlook; and various search engines for conducting Internet searches.
    • Strong verbal and written communication
    • Effective presentation
    • Ability to interface and work effectively within team and department with changing
    • Ability to frequently and accurately communicate with co-workers, customers, and vendors, via the telephone or by email.
    • Ability to exercise judgment and determine appropriate action to a variety of problems of varying
    • Ability to manage multiple
    • Analytical, problem solving and decision-making
    • Excellent attention to detail and organizational

     Education and Experience

    • Bachelor’s degree in the health or life sciences. Experience in a healthcare, clinical, or science related field preferred.
    • At least 1 year of experience in a clinical research setting (Clinical Trials Assistant, Study Coordinator, or similar), preferred.

     Physical Requirements

    • Ability to use computers daily in an interactive manner for extended periods of time and up to 8 hours per
    • Ability to sit and/or stand for an extended
    • Ability to travel (by land and air) on
    • Ability to lift and move up to 40 pounds on an occasional vasis.

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    Exact Sciences is 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 is available to any applicant or employee for inspection upon request. 

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