Minimum of 5 years of experience in global clinical trial management
Proven expertise in designing and executing clinical trials
Strong understanding of regulatory requirements
Exceptional analytical and problem-solving skills
Effective communication and interpersonal skills
Detail-oriented and organized
Responsibilities
Collaborate with cross-functional teams to develop and implement clinical trial protocols
Oversee and manage day-to-day operations of clinical trials
Analyze and interpret clinical trial data to identify trends
Proactively address challenges and implement solutions for trial execution
Communicate effectively with internal and external stakeholders
Benefits
Competitive base salary and performance-related incentives
Health and wellbeing programmes including medical, dental, and vision coverage
Retirement and pension plans
Life assurance and disability coverage
Employee assistance programmes and wellbeing resources
Learning and development opportunities through structured training
Full Job Description
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:
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.
Are you a current ICON Employee? Please click here to apply
About ICON plc
ICON plc is a global provider of drug development and commercialisation services to the pharmaceutical, biotechnology and medical device industries. The company specialises in the strategic development, management and analysis of programs that support clinical development. ICON has approximately 15700 employees in 40 countries. The company was founded in Dublin, Ireland in 1990 and is headquartered in Leopardstown, Dublin. ICON has been publicly traded on the NASDAQ since 1998.
