- Location
- UK, Reading, United Kingdom · Spain, Madrid · Hungary, Budapest · Regional Great Britain (Northern Ireland) · Bulgaria, Sofia · Romania, Bucharest · Czech Republic, Prague · Poland, Warsaw · Italy, Milan
- Workplace
- Remote
- Type
- Full-time
- Seniority
- Manager
- Education
- Bachelor
- Source
- Workday
Description
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 Clinical Trial Manager II at ICON, you will design and analyse clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies.
What You Will Do:
You will oversee clinical trial management workstreams, ensuring deliverables meet quality and timeline expectations.
Key responsibilities include:
- Collaborate with cross-functional teams to design and implement effective clinical trial enrollment Collaborating with cross-functional teams to develop and implement comprehensive clinical trial protocols.
- Overseeing and managing the day-to-day operations of clinical trials, ensuring compliance with regulatory standards.
- Analyzing and interpreting clinical trial data, identifying trends, and providing insights to optimize study outcomes.
- Proactively addressing challenges and implementing effective solutions to ensure the successful execution of clinical trials.
- Communicating effectively with internal and external stakeholders to foster strong partnerships and facilitate smooth trial processes.
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:
- Bachelor's degree in a relevant field, with a minimum of [X] years of experience in clinical trial management.
- Proven expertise in designing and executing clinical trials, with a strong understanding of regulatory requirements.
- Exceptional analytical and problem-solving skills, with the ability to interpret complex medical data.
- Effective communication and interpersonal skills, with the ability to collaborate across diverse teams.
- Detail-oriented and organized, with a track record of successfully managing multiple tasks and priorities simultaneously.
- 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.
Are you a current ICON Employee? Please click here to apply