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The Global Study Manager will oversee the day-to-day operations of clinical trials while ensuring compliance with regulatory standards. They will also collaborate with cross-functional teams to design protocols and analyze clinical trial data to optimize study outcomes.
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.
Job title - Global Study Manager/Project Manager
Location - EMEA, remote
Fully sponsor dedicated
We are currently seeking a Global Study Manager to join our diverse and dynamic team. As a Global Study Manager at ICON, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of innovative treatments and therapies.
What you will be doing
Collaborate with cross-functional teams to design and implement effective clinical trial enrollment Collaborating with cross-functional teams to develop and implement comprehensive clinical trial protocols.
Overseeing and managing the day-to-day operations of clinical trials, ensuring compliance with regulatory standards.
Analyzing and interpreting clinical trial data, identifying trends, and providing insights to optimize study outcomes.
Proactively addressing challenges and implementing effective solutions to ensure the successful execution of clinical trials.
Communicating effectively with internal and external stakeholders to foster strong partnerships and facilitate smooth trial processes.
Your profile
Bachelor's degree in a relevant field, with a minimum of 5 years of experience in global clinical trial management.
Proven expertise in designing and executing clinical trials, with a strong understanding of regulatory requirements.
Exceptional analytical and problem-solving skills, with the ability to interpret complex medical data.
Effective communication and interpersonal skills, with the ability to collaborate across diverse teams.
Detail-oriented and organized, with a track record of successfully managing multiple tasks and priorities simultaneously.
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:
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
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