Description
As a Clinical Research Associate at ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON's global expertise.
You will serve as the primary point of contact between investigational sites and the sponsor, conducting site visits, ensuring site compliance, and maintaining up-to-date documentation.
Responsibilities:
- Serve as primary point of contact between investigational sites and sponsor
- Conduct site visits, including selection, initiation, routine monitoring, and close-out
- Ensure site compliance with ICH-GCP, SOPs, and regulations
- Maintain up-to-date documentation in CTMS and eTMF systems
- Support and track site staff training and maintain compliance records
- Monitor patient safety and report adverse events
- Support subject recruitment and retention efforts
- Oversee drug accountability and ensure proper storage and destruction
- Resolve data queries and drive timely data entry
- Document site progress and escalate risks or issues
- Assist in tracking site budgets and ensuring timely site payments
- Collaborate with cross-functional partners
Requirements:
- Graduate with a Bachelor's degree in Life Sciences or equivalent, or a qualified RN
- Eligible to work in United States without visa sponsorship
- 2+ years of on-site monitoring experience in pharmaceutical or CRO industry
- Experienced across multiple therapeutic areas
- Proficient in ICH-GCP, local regulatory requirements, and clinical systems
- Clear communicator, problem-solver, and collaborative team player
- Willing and able to travel up to 50% for on-site monitoring visits
Rewards & 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