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.
🔥 2 minutes ago
Improve your chances of getting an interview by checking your resume score before you apply.
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.
• Lead medical affairs delivery across the portfolio, setting standards and developing the team • Provide strategic medical leadership and guidance on project teams • Offer expert medical and scientific consultation throughout project lifecycles • Ensure compliance with ethical, legal, and regulatory standards in medical and safety monitoring activities • Represent the Medical Affairs Department in business development initiatives • Provide operational oversight within the Medical Affairs Department as needed • Drive medical initiatives within project teams and guide strategic direction and decision-making • Leverage therapeutic expertise to inform project development
• Medical degree (MD) or equivalent qualification - Cardiology MD OR Endocrinology/Diabetes/Obesity or Internal Medicine MDs • Cardiovascular Outcomes trial experience or obesity/ GLP1 experience is a must for the role • Extensive experience in clinical research and development • 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 • Legal right to work in the country where the role is based
• 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
Apply Now🕒 September 25
Executive Director leading clinical pharmacology and pharmacometrics for Recursion’s rare disease and oncology drug programs. Guiding modeling, clinical studies, and regulatory submissions at a TechBio company.
🇬🇧 United Kingdom – Remote
💵 £136.5k - £167.2k / year
💰 $150M Post-IPO Equity on 2022-10
⏰ Full Time
🔴 Lead
👨⚕️ Medical Director
🕒 September 24
Associate Scientific Director leading scientific publications and medical affairs communications at Avalere Health, a healthcare consultancy. Guiding client accounts, strategic review, business development, and junior writer development.
🕒 July 1
Study Physician responsible for medical oversight and expertise in clinical trials at Parexel. Ensuring high quality protocol preparation and contributing to risk-based quality management with clinical insight.
🇬🇧 United Kingdom – Remote
💰 Venture Round on 1990-01
⏰ Full Time
🔴 Lead
👨⚕️ Medical Director
🇬🇧 UK Skilled Worker Visa Sponsor
🕒 June 23
Associate Medical Director at ApotheCom responsible for scientific content on oncology publications. Collaborating with clients and conducting literature searches to ensure accurate medical communications.
🕒 May 26
Medical Director providing strategic and operational input for pharmaceutical medical affairs. Leading cross-functional teams and collaborating on scientific initiatives in a global setting.