Medical Monitor

ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.

As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.

As a Medical Director, Clinical Research & Development at ICON, you will provide medical leadership and strategic direction to clinical development programs.

You will be partnering with a global pharmaceutical company passionate about transforming patients’ lives and committed to scientific rigor, unassailable ethics, and access to medical innovations for all. Key therapeutic area experience in Obesity and GLP 1 treatments is essential.

What You Will Do:

You will lead medical affairs delivery across your portfolio, setting standards and developing your team.

Key responsibilities include:

• Providing medical and scientific oversight for clinical trials, ensuring that study protocols are scientifically sound and aligned with regulatory requirements.
• Collaborating with clinical operations, regulatory, and safety teams to drive the successful execution of clinical development programs.
• Developing and reviewing clinical study protocols, investigator brochures, and other key study documents.
• Interpreting clinical trial data and providing medical insights to inform decision-making and guide clinical development strategies.
• Building relationships with key opinion leaders, investigators, and external stakeholders to support clinical development initiatives.

Your Profile:

You will bring significant medical affairs experience, with a track record of building high-performing teams and delivering results.

Required qualifications and experience:

• 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.
• Willingness to travel as required (approximately 10%)

Employment with ICON is contingent upon having the legal right to work in the country where the role is based.

Rewards & Benefits

ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.

Benefits may include:

• 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

Benefits may vary depending on role and location.

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

Inclusion and Accessibility

ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.

If you require reasonable accommodations during the recruitment process, please let us know or submit a request here.

Are you a current ICON Employee? Please click here to apply