Medical Director

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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

• Serve as a medical responsible on clinical trial(s), overseeing execution of clinical trial activities in assigned projects • Engage and work with Key Opinion Leaders or Scientific Advisors in the relevant therapeutic area to help develop scientific rationale for clinical trials • Develop and/or oversee the preparation of clinical development plans, study concept sheets, study protocols or regulatory documentation in collaboration with clinical and project team members for assigned indication(s)/products or with external partners for collaborative studies • Actively contribute to or oversee medical writing of medical sections of study protocols, investigator brochure and other regulatory documents • Manage the clinical team supporting the clinical trial • Oversee all aspects related to the scientific and medical risk in collaboration with the safety representative and other relevant stakeholders • Support the review, analysis and interpretation of study data • Support communication of study results as assigned

🎯 Requirements

• Medical Degree (mandatory) • Neuroimmunology experience is a must • Myasthenia gravis experience would be a big plus • Able to communicate effectively in English • Experience leading protocol development • Requires substantial professional experience in related TA/indication including clinical trials • Professional experience in the execution of clinical trials as medical responsible (3+ years) • Previous experience in medical monitoring, medical data review, eligibility review during recruitment, presentations at investigator meetings and trainings, protocol writing, regulatory responses • Experience in design, set up, conduct and evaluation of clinical trials • Experience working in a cross-functional multi-site team environment • Working knowledge of GCP, ICH, US FDA and EMA regulations

🏖️ 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