Senior Clinical Trial Manager

🔥 13 hours ago

🔔 Pennsylvania – Remote

🔔 Pennsylvania – Remote

⏰ Full Time

🟠 Senior

🧪 Clinical Research

👻 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

• Manage clinical trial operations activities, supporting the team and stakeholders to deliver high-quality outcomes across clinical programmes. • Coordinate clinical trial management delivery. • Resolve issues and develop team capability. • Oversee the clinical portion of the budget to ensure efficient resource allocation. • Develop monitoring plans and tools to ensure effective study oversight. • Train and mentor Clinical Research Associates (CRAs) to optimize performance. • Drive enrollment and lead study start-up activities while adhering to timelines. • Review trip reports and implement corrective and preventative action plans when necessary. • Foster productive relationships with Sponsors, vendors, and cross-functional teams.

🎯 Requirements

• A minimum of 5- 7 years of global Clinical Trial Management experience at a CRO or Pharmaceutical Organization. • Bachelor's degree in health, life sciences, or other relevant fields of study. • At least 10+ years of relevant experience in clinical trial management. • Preferred: 2+ years of monitoring experience. • Experience in managing complex or global trials is advantageous. • Preferred: Experience in managing all trial components from start-up to database lock. • Preferred: Experience in coaching/mentoring other CTMs, leading a team of CTMs, and participating in departmental initiatives. • Willingness to travel as required (approximately 25%). • Employment with ICON is contingent upon having the 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