Medical Affairs Lead, Solid Tumor

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ICON plc

WebsiteLinkedInAll Job Openings

10,000+ employees

Founded 1990

💊 Pharmaceuticals

🧬 Biotechnology

⚕️ Healthcare Insurance

Pharmaceuticals • Biotechnology • Healthcare Insurance

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

• Constantly builds and maintains expertise in assigned areas regarding available literature, treatment options, disease environment and product data • Gains in-depth knowledge in early development indications and analyzes different data sources resulting in meaningful reports and derived strategies • Identifies and engages with internal and external experts for participation in medical communications and content development • Provides oversight and contributes to the preparation and delivery of high-quality content and medical communication materials • Streamlines product communication and works on the development of multi-channel communication strategies and medical event planning • Acts as medical point of contact for clinical studies within solid tumor indications and provides continuous support to study centers and the ClinOps Team

🎯 Requirements

• MD, PharmD or PhD in life sciences • Long standing experience in the pharmaceutical industry, preferably in oncology • 5-7 years of relevant working experience in similar roles • Proven track record in preparing for product launches and successful life cycle management • Knowledge in development and implementation of clinical trials • Experienced in material review in the role of an Information Officer • Excellent communication skills and ability to present scientific data

🏖️ 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