Medical Director

ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.

About the role

As a Medical Director at ICON, you will drive medical initiatives within project teams, guiding strategic direction and decision-making processes, and offer expert medical and scientific guidance, leveraging therapeutic expertise to inform project development.

• Serve as the Global Clinical Lead and Medical Monitor for one or more studies, including participation on the clinical sub-teams of those programs.
• Contribute directly to the authoring of protocols, clinical study reports, study documents, regulatory documents, and external publications.
• Provide medical review of clinical trial data and medical monitoring of clinical trials.
• Interact with senior management regarding data presentations, trial updates, and discussions of executional and strategic development issues.
• Contribute to strategic discussions related to clinical development plans and indication prioritization.
• In collaboration with Clinical Operations, oversee and coordinate the operational aspects of ongoing projects to ensure time, cost, and quality objectives are met.
• Ensure Clinical Development Standard Operating Procedures (SOPs) facilitate effective clinical research programs and comply with clinical, medical, and industry standards.
• Review and contribute to regulatory documents and regulatory interactions as needed.

Requirements

• MD with residency training in Psychiatry and extensive drug development experience in psychiatry, including Phase I–III clinical development in schizophrenia, bipolar disorder, ADHD, and major depressive disorder.
• Five or more years of experience in the pharmaceutical industry in a Clinical Development role as a Medical Director.
• Outstanding written and verbal communication skills, with experience interacting with and presenting to senior management and external audiences.
• Ability to manage complexity and ambiguity in a highly matrixed work environment.
• Strong leadership and collaborative interpersonal skills.
• Ability to work independently, prioritize tasks effectively, and meet expected timelines.
• Ability to perform thorough reviews of medical and clinical trial-related documents in a timely manner.

Benefits

Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent. In addition to your competitive salary, ICON offers a range of additional benefits.

• Various annual leave entitlements
• A range of health insurance offerings to suit you and your family’s needs.
• Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.
• Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family’s well-being.
• Life assurance
• Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others.

Visit our careers site to read more about the benefits ICON offers.