Home Health Study Manager

Job not on LinkedIn

🔥 0 minutes ago

🔔 Pennsylvania – Remote

🔔 Pennsylvania – Remote

⏰ Full Time

🟢 Junior

🟡 Mid-level

👔 Manager

👻 Ghost score 10%

What it means: how likely this posting is sitting open without active hiring.How to read it: 60% or higher means we think this is a ghost. Lower scores are less of a worry.How we score it: age, reposts, open roles vs team size, how fast jobs close, and whether pay is listed.Fine print: an estimate from public data, not a judgment of the company. Real jobs can score high, so treat it as a hint, not a fact.

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ICON plc

WebsiteLinkedInAll Job Openings

10,000+ employees

Founded 1990

💼 Consulting

🏥 Healthcare

📦 Logistics

Consulting • Healthcare • Logistics

ICON plc is a global provider of clinical, consulting, and commercial services across various sectors in the healthcare and pharmaceutical industries. They offer a wide range of clinical solutions, including decentralised clinical trials, cardiac safety solutions, early clinical laboratories, and medical imaging. ICON also provides technology solutions that support drug development from early phases to post-marketing. Their therapeutic expertise spans cardiovascular, oncology, internal medicine, and more, with a strong focus on transformative therapies like cell and gene therapies and biosimilars. ICON is recognized as a leading Contract Research Organisation (CRO), regularly providing thought leadership and contributing to industry publications and events. Their services are tailored to optimize clinical trials, offer regulatory intelligence, and deliver real-world evidence through robust data analysis and patient-centric solutions.

📋 Description

• 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 provides quality service • Provide support and guidance for all resources, including routine teleconferences to review progress, timelines, issue management, and information sharing • Contact necessary staff to ensure tasks are scheduled and have occurred per required timelines • Review study documentation for completeness, accuracy, and timeliness, and seek or correct documentation as needed • Ensure study information is updated and reports are reviewed and provided to appropriate stakeholders according to expected timelines • Solicit information to support inquiries from all stakeholders • Support internal and external team members in their efforts to support the study • Participate in and lead study team reviews • Act as liaison between the sponsor, CRO, investigative site staff, laboratory, pharmacy, and other personnel • Represent the 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 contracted study visits are completed on schedule, documentation is timely, complete, and accurate, and lab samples are evaluable

🎯 Requirements

• 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 • Legal right to work in the country where the role is based

🏖️ Benefits

• 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