Medical Monitor

Job not on LinkedIn

🕒 August 4

🇺🇸 United States – Remote

⏰ Full Time

🟡 Mid-level

🟠 Senior

🧪 Clinical Research

👻 Ghost score 45%

What it means: the chance that no one is really hiring for this job.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

• Provide medical leadership and strategic direction to clinical development programs • Lead medical affairs delivery across the portfolio • Set standards and develop the team • Provide medical and scientific oversight for clinical trials • Ensure study protocols are scientifically sound and aligned with regulatory requirements • Collaborate with clinical operations, regulatory, and safety teams • Develop and review clinical study protocols, investigator brochures, and other key study documents • Interpret clinical trial data and provide medical insights for decision-making and clinical development strategies • Build relationships with key opinion leaders, investigators, and external stakeholders

🎯 Requirements

• Medical degree (MD) or equivalent qualification • Extensive experience in clinical research and development, preferably within the pharmaceutical or biotechnology industry • Strong understanding of clinical trial design, regulatory requirements, and GCP guidelines • Exceptional analytical and problem-solving skills, with a focus on interpreting clinical data and driving evidence-based decisions • Excellent leadership, communication, and collaboration skills, with the ability to work effectively in cross-functional, global teams • Experience in monitoring Obesity/GLP-1 studies • Board certified professional • Willingness to travel as required (approximately 10%) • 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

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