We have an incredible opportunity for a Home Health Study Manager to join ICON’s Accellacare In-Home Care team. The Study Manager’s primary responsibility is to coordinate and manage all contracted services in assigned studies, 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.

This role is with , part of ICON's clinical research network, where you’ll play a key role in transforming the clinical trial experience for patients and sponsors alike. Our global site network is designed with one goal in mind: to deliver better access, greater efficiency, and improved outcomes in clinical research.

Location: Eastern or Central Time Zone - United States (Remote)

What you will be doing:

• Coordinate, administer, and document all study management activities while maintaining and adhering to study project plans and timelines
• Train assigned staff (including subcontracted resources) and ensure staff is providing quality service
• Provide support and guidance for all resources, including routine teleconferences to review progress to timelines, issue management, and information sharing
• Contact necessary staff to ensure tasks are scheduled and have occurred per the required timelines
• Review study documentation to ensure completeness, accuracy and timeliness, and seek or correct documentation, as needed
• Ensure study information is updated and reports are reviewed and provided to the appropriate stakeholders 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
• Participate in and lead study team reviews
• Act as the liaison between the sponsor, CRO, investigative site staff, laboratory, pharmacy and other internal and external personnel as the study requires
• Represent department effectively and professionally in project calls, webinars, teleconferences, and meetings
• Comply with ICH/GCP, IATA, HIPAA, and other appropriate regulations, policies and procedures
• Ensure overall study deliverables and that contracted study visits are completed on schedule, documentation is timely, complete, and accurate, and lab samples are evaluable

Your profile:

• 2+ years of experience as a Clinical Research Coordinator, Clinical Research Associate, or similar clinical research role coordinating study startup, operational activities, and study closeout processes
• Exceptional attention to detail and organizational skills, with the ability to effectively manage multiple priorities and complex study activities concurrently
• Strong problem-solving skills with the ability to quickly assess situations, identify solutions, and resolve operational challenges
• Laboratory knowledge (preferred)
• Bachelor's degree, preferably in a life sciences, healthcare, or related field

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Employment with ICON is contingent upon having the legal right to work in the country where the role is based.

Rewards & Benefits

ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.

Benefits may include:

• Competitive base salary and performance related incentives
• Health and wellbeing programmes including medical, dental, and vision coverage where applicable
• Retirement and pension plans
• Life assurance and disability coverage
• Employee assistance programmes and wellbeing resources
• Learning and development opportunities through structured training and career pathways

Benefits may vary depending on role and location.

Visit our to read more about the benefits ICON offers.