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.

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.

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

Global Study Manager

Key skills