Description
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.
We are currently seeking a Senior Clinical Trial Manager to join our diverse and dynamic team at ICON Plc. In this critical role, you will be responsible for overseeing the planning, execution, and successful completion of clinical trials, ensuring adherence to timelines, budgets, and regulatory guidelines. As a leader in our research department, you will collaborate with cross-functional teams, manage site relationships, and provide strategic guidance to drive the successful delivery of clinical trial outcomes.
Responsibilities
Your focus will be on coordinating clinical trial management delivery, resolving issues, and developing team capability. Key responsibilities include:
- Budget Oversight: Oversee the clinical portion of the budget to ensure efficient resource allocation.
- Ensuring Effective Study Oversight: Develop monitoring plans and tools, ensuring effective study oversight.
- Optimizing Performance: Train and mentor Clinical Research Associates (CRAs) to optimize their performance.
- Timely Study Start-Up & Enrollment: Drive enrollment and lead study start-up activities, adhering to timelines.
- Improving Study Integrity: Review trip reports and implement corrective and preventative action plans when necessary.
- Building Productive Relationships: Foster productive relationships with Sponsors, vendors, and cross-functional teams.
Requirements
You will have solid clinical trial management experience, with the ability to manage competing priorities and develop your team. Required qualifications and experience:
- A minimum of 4+ years of experience in a Clinical Trial Management position at a CRO or Pharmaceutical Organization.
- Bachelor's degree in health, life sciences, or other relevant fields of study.
- At least 10+ years of relevant experience in clinical trial management.
- Preferred: 2+ years of monitoring experience.
- Experience supporting complex protocols, including areas such as MASH/NASH, Radiopharmaceutical, or other specialized therapeutic programs, is highly valued.
- Experience in managing complex or global trials is advantageous.
- Preferred: Experience in managing all trial components from start-up to database lock.
- This role is intended for experienced CTM professionals; entry-level CTM experience alone will not meet the requirements.
- Willingness to travel as required (approximately 25%).
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.