Lead clinical project activities with ICON plc as a Project Manager. Ensure timely and quality delivery of study operations while managing resources and stakeholder communication effectively. In this pivotal role, you will oversee and coordinate country and regional study operations from startup to closure.

As a Project Manager, you will manage country-level activities, ensuring compliance with protocols, and provide oversight on study execution. This includes working closely with internal teams, pCROs, and the local Study Team to meet quality standards and mitigate risks. Key Responsibilities:
Manage oversight of study startup through to completion
Coordinate with pCRO for country-level activities




Support site identification and feasibility assessments
Ensure compliance with global and local regulations
Facilitate effective communication between teams Requirements:
BS/BSc/MS/MSc with 5+ years clinical trial experience
Expertise in GCP and regulatory operations
Proven experience in project management and study oversight
Solid communication and analytical skills
Ability to identify and mitigate risks effectively Shape the future of clinical development through your leadership and operational expertise at ICON.

📌 Project Manager For Clinical Studies At Icon Burlington
🏢 Icon
📍 Burlington