- Location
- UK, Reading, United Kingdom · Italy, Rome · Spain, Madrid · Spain, Barcelona · Bulgaria, Sofia · Romania, Bucharest · Greece, Athens · Poland, Gdansk · Czech Republic, Prague · Poland, Warsaw · Italy, Milan · South Africa, Johannesburg
- Workplace
- Remote
- Type
- Full-time
- Seniority
- Manager
- Visa
- Not sponsored
- Source
- Workday
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.
As a Clinical Trial Manager at ICON, you will manage clinical trial operations activities on a global level, supporting your global team and stakeholders to deliver high-quality outcomes across our clinical programmes and feeding into the Global Project Manager.
What You Will Do:
You will manage day-to-day clinical trial management activities, supporting your team to deliver quality outcomes at a study management level
Key responsibilities include:
- Plan and manage all aspects of clinical trials, ensuring adherence to timelines, vendor budget, and quality standards.
- Collaborate with cross-functional teams to establish and implement clinical trial protocols and procedures.
- Build and manage strong relationships with global stakeholders
- Vendor management - setting up vendors, leading vendor calls for their performance and KPIs as well as managing vendor budgets
- Ensure all trials are conducted in compliance with local, national, and international regulations and ethical guidelines.
- Problem-solve and make critical decisions regarding trial design, vendor selection, and risk management.
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:
- University degree in medicine, science, or equivalent combination of education & experience
- Minimum of 5 years in Clinical Research industry working within a Pharma or CRO
- Must have vendor management experience including setting up, leading performance calls with vendors
- Global cross-functional experience in presenting for your studies
- Demonstrated ability to drive the clinical deliverables of a study
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
