Global Study Manager, CVRM at ICON plc

Job Title:

Global Study Manager, CVRM

Employer:

ICON plc
Job Type: Remote

Location:

United Kingdom
Salary/Rate:
Not Specified
UK Skilled Worker Visa Sponsorship:
Not Available

• Support global clinical studies from protocol development through study completion and archiving.
• Coordinate with internal stakeholders, Contract Research Organisations (CROs), and external vendors worldwide.
• Ensure clinical trials are delivered on time, within budget, and in compliance with quality and regulatory standards.
• Support innovative clinical research programmes, including global cardiovascular trials.
• Collaborate with cross-functional international teams to deliver clinical research objectives.

• Degree in Life Sciences, Medical Sciences, Biological Sciences, or a related field.
• Must be based in the UK and have the legal right to work in the country where the role is based.
• At least 3 years of global trial management experience in clinical research, pharmaceuticals, biotechnology, or a CRO environment.
• Strong understanding of clinical development and the drug development process.
• Excellent knowledge of ICH-GCP guidelines and global clinical trial regulations.
• Proven project management, organisational, communication, and stakeholder management skills.
• Experience working effectively with global, cross-functional teams.
• Previous experience supporting cardiovascular clinical trials is highly desirable.
• Proactive, collaborative, and able to work independently in a fast-paced environment.

• 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 progression pathways.