Study Manager Home Health

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 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 timelinesTrain subcontracted resources, country study managers, nurses or other cliniciansProvide support and guidance for subcontracted resources, including routine teleconferences to review progress to timelines, issue management, and information sharingContact country study managers and/or clinicians to ensure visits are scheduled and have occurred per the required timelinesReview study documentation to ensure completeness, accuracy and timelinessSeek or correct documentation, as neededEnsure CRM is updated, reports are reviewed and provided to the appropriatestakeholders timely and according to expected timelinesSolicit information to support inquiries from all stakeholdersSupport all internal and external team members in their efforts to support the studyAssist in training new team membersEnsure Symphony is providing quality serviceAct as the liaison between the sponsor, CRO, investigative site staff, laboratory, pharmacy and other internal and external personnel as the study requiresRepresent Symphony effectively and professionally in project calls, webinars, teleconferences and meetingsRecognize sensitive issues and manage them effectively; escalate up when need assistanceComply with ICH/GCP, IATA, HIPAA and other appropriate regulations, policies and proceduresEnsure that contracted study visits are completed on schedule, documentation is timely, complete and accurate and lab samples are evaluableProvide support and oversight for project financials and forecastingPerform other duties as assigned

Role Requirements:Bachelors' Degree (preferably in the life sciences or healthcare field)4+ years CRA/ Study Coordinator or related experience requiredHomecare experience preferredKnowledge of clinical trial terminology and practices highly desirableSome leadership experienceTraining 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.