About the role
Sr. Clinical Trial Manager
- At ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON’s global expertise.
- As the world’s largest FSP organisation, with over 90 sponsor partnerships, we offer stability, career development and a collaborative environment where your work contributes to the development of treatments that benefit patients worldwide.
- As a Senior Clinical Trial Manager at ICON, you will manage clinical trial operations activities, supporting your team and stakeholders to deliver high-quality outcomes across our clinical programmes.
- What You Will Do: 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.
- Your Profile: 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 in managing complex or global trials is advantageous.
- Preferred: Experience in managing all trial components from start-up to database lock.
- Preferred: Experience in coaching/mentoring other CTMs, leading a team of CTMs, and participating in departmental initiatives.
- Willingness to travel as required (approximately 25%)
- 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
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- Are you a current ICON Employee? Please click here to apply