Clinical Trial Manager (TO)

ICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organisations.

With our patients at the centre of all that we do, we help to accelerate the development of drugs and devices that save lives and improve quality of life.

Our people are our greatest strength, are at the core of our culture, and the driving force behind our success. ICON people have a mission to succeed and a passion that ensures what we do, we do well.

That’s our vision. We’re driven by it. And we need talented people who share it.
If you’re as driven as we are, join us. You’ll be working in a dynamic and supportive environment, with some of the brightest and the friendliest people in the sector, and you’ll be helping shape an industry.

Overview of the role: ICON plc, a global leader in clinical research, is seeking a highly skilled and motivated Clinical Trial Manager to join our dynamic team in Poland or Spain. This role is crucial in overseeing and managing the execution of clinical trials, ensuring adherence to protocols, timelines, and quality standards.

Responsibilities:

• Lead the planning, implementation, and execution of clinical trials in compliance with regulatory requirements and company SOPs.
• Act as the primary point of contact for internal and external stakeholders, ensuring effective communication and collaboration throughout the trial lifecycle.
• Manage study timelines, budgets, and resources, providing proactive solutions to challenges that may arise.
• Oversee the selection and management of study sites, CROs, and vendors to ensure trial success.
• Monitor trial progress, identify potential risks, and implement mitigation strategies to maintain study quality and timelines.
• The CTM will also participate in Sponsor, Investigator and bid defense meetings.

Qualifications:

• Bachelor's degree in a relevant field (Life Sciences, Nursing, or equivalent).
• Extensive experience in clinical trial management, demonstrating a successful track record in the pharmaceutical or CRO industry.
• Strong leadership, organizational, and problem-solving skills.
• Thorough knowledge of ICH-GCP guidelines and local regulatory requirements.
• Excellent communication and interpersonal abilities, with a proven capacity to manage multiple stakeholders effectively.

Why Join ICON?

• Be part of a global leader in clinical research, contributing to groundbreaking advancements in healthcare.
• Collaborative work environment with ample opportunities for professional growth and development.
• Competitive compensation and benefits package.
• Contribute to innovative research and make a tangible impact on patient well-being.

Benefits of Working in ICON:

ICON is an equal opportunity and inclusive employer and 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 through the form below.

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