We currently have an exciting opportunity for an experienced
Global Clinical Project Manager
to join a successful sponsor-dedicated program. This is a
business-critical role
within Study Management, BioPharmaceuticals Clinical Operations, focused on the
delivery of clinical studies .
Role OverviewThe
Global Clinical Project Manager
leads cross-functional study teams, providing direction and guidance to ensure successful study delivery. They act as the main liaison between the study team and the Clinical Program Team (CPT), from study handover through to close-out. The role is accountable for delivering studies on time, within budget, and to quality standards by fostering effective partnerships and teamwork, both internally and with external partners.
Key Responsibilities
Lead and oversee study activities, ensuring milestones are met within scope, time, and budget.
Facilitate communication across all functions and external partners.
Conduct investigator meetings and other study-related meetings.
Develop and maintain essential study documents, including protocols and reports.
Manage external service providers, ensuring performance aligns with contracted goals and timelines.
Create and update study plans, including quality and risk management strategies.
Ensure accuracy of information across all study systems.
Monitor study performance against plans and KPIs, reporting risks and issues with mitigation strategies.
Proactively communicate findings and CAPAs to stakeholders.
Oversee Trial Master File (TMF) completion and quality control activities.
Ensure compliance with governance controls and manage study budgets, including re-forecasting and financial risk mitigation.
Qualifications
University degree in medical, biological sciences, or related field.
At least 5 years of relevant clinical industry experience, including 2 years in project management.
Advanced degree (Masters or higher) preferred.
Project management certification.
Proven experience managing global clinical studies.
Extensive knowledge of ICH-GCP and clinical research regulations.
Strong leadership, communication, and organizational skills.
Experience working in Pharma or CRO settings within global study delivery.
Legal right to work in Spain, UK, Poland, or Bulgaria without sponsorship.
This is a
permanent, fully home-based
position with ICON, available in the specified countries.
#J-18808-Ljbffr