Laboratory Study Manager

What ICON can offer you:
Our success depends on the quality of our people. That's why we've made it a priority to build a diverse culture that rewards high performance and nurtures talent.

In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.

Our benefits examples include:

• Various annual leave entitlements
• A range of health insurance offerings to suit you and your family's needs.
• Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.
• Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family's well-being.
• Life assurance
• Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others.

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.

Laboratory Study Manager sponsor dedicated - EMEA (various locations) - remote

As a Clinical Study Manager at ICON being assigned to a single sponsor as Biosamples Study Manager, you will design and analyze clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies.

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.