Senior Clinical Trial Associate

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 Trial Associate at ICON, you will oversee and support the execution of clinical trials, ensuring the highest standards of quality, compliance, and efficiency. This is a sponsor dedicated position focused on Oncology trials.

What You Will Do:

You will lead on clinical coordination tasks requiring technical depth, with a focus on quality and continuous improvement.

Key responsibilities include:

• Managing and coordinating clinical trial activities to ensure adherence to protocols, regulatory requirements, and project timelines.
• Collaborating with cross-functional teams to address clinical trial issues, optimize processes, and ensure the effective execution of studies.
• Overseeing site management and monitoring to ensure data integrity and compliance with study protocols.
• Providing guidance and support to clinical staff and investigators, ensuring adherence to best practices and regulatory standards.
• Tracking and reporting on trial progress, identifying potential risks, and implementing strategies to mitigate challenges.

Your Profile:

You will have a strong foundation in clinical coordination, with the experience to work independently and guide others.

Required qualifications and experience:

• Bachelor's degree in a relevant scientific discipline or healthcare-related field
• Significant experience in clinical trial management, with a strong understanding of clinical trial processes and regulatory requirements.
• Proven ability to manage multiple projects effectively, with strong organizational and problem-solving skills.
• Excellent communication and interpersonal skills, with the ability to collaborate effectively with diverse teams and stakeholders.
• Detail-oriented with a proactive approach to ensuring trial success and addressing clinical challenges.
• Oncology experience required

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