Study Manager Home Health
About the role
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Our 'Own It' culture is driven by four key values that bring us together as individuals and set us apart as an organisation: Accountability & Delivery, Collaboration, Partnership and Integrity. We want to be the Clinical Research Organisation 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.
Are you an experienced Study Manager with experience in home health? Are you passionate about playing a key role in driving innovative solutions within home health for clinical research studies?
As part of the ICON family now, Accellacare Home Health is the global leader in home health clinical trials making it convenient for patients to participate in clinical research by taking study visits to where they live, work, study or play!
Study Manager role within Accellacare Home Health at ICON plc
The Study Manager's primary responsibility is to coordinate and manage all
Accellacare Home Health-contracted services in assigned study(s), providing quality service, and exceeding the expectations of our customers. The Study Manager manages the key relationships and communication among all internal and external stakeholders involved in a study, keeping all stakeholders informed in a timely and professional manner about the progress and key events with the study. The Study Manager is expected to accurately identify issues and creatively resolve problems while correcting processes as needed.
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 routine teleconferences 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 appropriate
- stakeholders 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 and other internal and external personnel as the study requires
- Represent Symphony effectively and professionally in project calls, webinars, teleconferences and 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
- Provide support and oversight for project financials and forecasting
- Perform other duties as assigned
Role Requirements:
- Bachelors' Degree (preferably in the life sciences or healthcare field)
- 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
Benefits of Working in ICON:
Our success depends on the quality of our people. That's why we've made it a priority to build a culture that rewards high performance and nurtures talent.
We offer very competitive salary packages. And to keep them competitive, we regularly benchmark them against our competitors. Our annual bonuses reflect delivery of performance goals - both ours and yours.
We also provide a range of health-related benefits to employees and their families and offer competitive retirement plans - and related benefits such as life assurance - so you can save and plan with confidence for the years ahead.
But beyond the competitive salaries and comprehensive benefits, you'll benefit from an environment where you are encouraged to fulfil your sense of purpose and drive lasting change.
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.
A better career. A better world. A better you.
Our people are our greatest strength, are the core of our culture and the driving force behind our success. Throughout all levels of the company, our people have a drive to succeed and a passion that ensures what we do, we do well. We help you build exciting and rewarding careers, deliver results to help bring life-changing medicine and devices to market and maintain ICON’s success as an industry leader. See all locations Read more
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