Study Manager - Home Health

Study Manager - Home Health

01 Oct 2024
Missouri, Springfield, 65801 Springfield USA

Study Manager - Home Health

Vacancy expired!

At ICON, it’s our people that set us apart. Our diverse teams enable us to become a better partner to our customers and help us to fulfil our mission to advance and improve patients’ lives.Our ‘Own It’ culture is driven by four key values that bring us together as individuals and set us apart as an organization: Accountability & Delivery, Collaboration, Partnership and Integrity. We want to be the Clinical Research Organization that delivers excellence to our clients and to patients at every touch-point. In short, to be the partner of choice in drug development.That’s our vision. We’re driven by it. And we need talented people who share it.If you’re as driven as we are, join us. You’ll be working in a dynamic and supportive environment, with some of the brightest and the friendliest people in the sector, and you’ll be helping shape an industry. Overview of the role: Title : Study Manager, Home Health Location: Remote- US Job Description: Coordinate, administer and document all study management activities to include: Maintain and adhere to study project plans and timelines Train subcontracted resources, country study managers, nurses or other clinicians Provide support and guidance for subcontracted resources, including routineteleconferences to review progress to timelines, issue management, and information sharing Contact country study managers and/or clinicians to ensure visits are scheduled and have occurred per the required timelines Review study documentation to ensure completeness, accuracy and timeliness Seek or correct documentation, as needed Ensure CRM is updated, reports are reviewed and provided to the appropriatestakeholders timely and according to expected timelines Solicit information to support inquiries from all stakeholders Support all internal and external team members in their efforts to support the study Assist in training new team members Ensure Symphony is providing quality service Act as the liaison between the sponsor, CRO, investigative site staff, laboratory, pharmacy andother internal and external personnel as the study requires Represent Symphony effectively and professionally in project calls, webinars, teleconferencesand meetings Recognize sensitive issues and manage them effectively; escalate up when need assistance Comply with ICH/GCP, IATA, HIPAA and other appropriate regulations, policies and procedures Ensure that contracted study visits are completed on schedule, documentation is timely,complete and accurate and lab samples are evaluable Perform other duties as assigned To be successful you will need: Bachelors Degree, preferably in the life sciences or healthcare field Minimum 4 years CRA/Study Coordinator or related experience required Homecare experience preferred Knowledge of clinical trial terminology and practices highly desirable Some leadership experience Training external and internal team members ICON is an equal opportunity and inclusive employer and is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know through the form below.

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Job Details

  • ID
    JC46142761
  • State
  • City
  • Full-time
  • Salary
    N/A
  • Hiring Company
    ICON Clinical Research
  • Date
    2022-10-01
  • Deadline
    2022-11-29
  • Category

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