Description
ICON is seeking a Medical Monitor to provide medical leadership and strategic direction to clinical development programs.
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.
Requirements:
- 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%).
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.