Laboratory Study Manager

ICON Clinical Research; City of Rome (NY); Hybrid; USD 95,000 - 150,000; Full time

Benefits offered by this job

Annual leave entitlements

Health insurance offerings

Retirement planning

Employee Assistance Programme

Life assurance

Flexible country-specific benefits

Job summary

ICON Strategic Solutions is seeking a Laboratory Study Manager sponsor-dedicated role in a remote setting across the EMEA region. The role focuses on coordinating clinical trial delivery, resolving issues, and building team capability, while ensuring regulatory compliance and high data quality.

The candidate will design and analyze trials, manage budgets and timelines, and collaborate with external partners to advance treatments that benefit patients worldwide.

Qualifications

• Bachelor's degree in a relevant scientific discipline or healthcare-related field.
• Proven experience in clinical study management within drug development.
• Strong project management skills with ability to multitask.
• Excellent communication and stakeholder management abilities.
• Detail-oriented with focus on data accuracy and quality.

Responsibilities

• Oversee planning, execution, and monitoring of clinical trials to meet timelines and regulatory requirements.
• Collaborate with investigators, vendors, and internal teams to drive study success.
• Develop and manage study budgets, resources, and timelines for efficient operations.
• Lead issue resolution and risk management throughout the study lifecycle.
• Ensure data integrity and quality through rigorous monitoring and validation.

Skills

Project management

Communication

Cross-functional collaboration

Attention to detail

Education

Bachelor's degree in a scientific/healthcare field

Job description

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

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 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.

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.

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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.

Visit our careers site (https://careers.iconplc.com/benefits) to read more about the benefits ICON offers.

At ICON, inclusion & belonging are fundamental to our culture and values. We’re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.

If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here (https://careers.iconplc.com/reasonable-accommodations)