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 Senior Clinical System Lead at ICON, you will be instrumental in overseeing the design, development, and implementation of clinical systems that drive the efficiency and effectiveness of clinical trials.

What You Will Do:

You will manage day-to-day scientific operations activities, supporting your team to deliver quality outcomes.

Key responsibilities include:

• Leading the design, development, and implementation of clinical systems, ensuring they meet all functional and regulatory requirements.

• Coordinating with cross-functional teams to define system needs, set specifications, and deliver solutions that enhance clinical trial management and data analysis.

• Overseeing the integration of clinical systems with other technologies and data sources to ensure seamless operation and data consistency.

• Providing strategic guidance on system enhancements, troubleshooting complex issues, and driving continuous improvements in system performance.

• Managing relationships with system vendors and stakeholders to ensure the timely delivery of system updates, support, and alignment with clinical research objectives.

Your Profile:

You will have solid scientific operations experience, with the ability to manage competing priorities and develop your team.

Required qualifications and experience:

• Degree in computer science, software engineering, or a related field.

• Minimum 5 years of relevant experience in Project Management and/or Designing
• Must have client-facing experience
• Strong stakeholder management skills
• Ability to interpret clinical protocols
• Exposure to Medidata Rave and Veeva is an added advantage
• Willingness to work in 2 PM – 11 PM shift
• Extensive experience in leading the development and implementation of clinical systems, with a deep understanding of clinical trial processes and regulatory requirements.
• Strong leadership skills, with proven ability to manage cross-functional teams and projects effectively.
• Proficiency in relevant programming languages and development tools, with experience in system integration and data management.
• Excellent communication and interpersonal skills, with a demonstrated ability to collaborate with diverse teams and external partners.
• Willingness to travel as required (approximately 15%)

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