Laboratory Study Manager

Job Description:

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

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 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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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