Clinical Study Manager

Clinical Study 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 Clinical Study Manager 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: Your focus will be on coordinating clinical trial management delivery, resolving issues, and developing team capability.
• Key responsibilities include: Oversee the planning, execution, and monitoring of clinical trials to ensure compliance with regulatory requirements and project timelines.
• Collaborate with cross-functional teams, including investigators, vendors, and internal stakeholders, to drive the successful implementation of clinical studies.
• Develop and manage study budgets, resources, and timelines, ensuring efficient use of resources and adherence to study plans.
• Lead the resolution of issues and challenges that may arise during clinical trials, employing effective problem-solving skills and communication strategies.
• Ensure data integrity and quality by implementing rigorous monitoring and validation processes throughout the study lifecycle.
• 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 scientific discipline or healthcare-related field
• Proven experience in clinical study management, with a strong understanding of the drug development process and regulatory requirements.
• Excellent project management skills, including the ability to handle multiple tasks simultaneously and prioritize effectively.
• Strong communication and interpersonal skills, with the ability to collaborate effectively with cross-functional teams and external partners.
• Detail-oriented with a focus on ensuring data accuracy and maintaining high-quality standards in clinical trials.
• 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