About this role
About the Role Clinical Research Associate to serve as the primary point of contact between investigation sites and sponsor for early development multi-therapeutic trials across regional hubs. Responsible for site visits, regulatory compliance, documentation in CTMS/eTMF, safety monitoring, recruitment support, and data integrity to enable timely trial execution. What You'll Do
- Serve as primary point of contact between investigation sites and sponsor for early development multi-therapeutic trials.
- Conduct site visits including selection, initiation, routine monitoring, and close-out.
- Ensure site compliance with ICH-GCP, SOPs, and applicable 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 ensure timely AE/SAE/PQC reporting.
- Support subject recruitment and retention at the site level.
- Oversee drug accountability and proper storage, return, or destruction.
- Resolve data queries and drive timely, high-quality data entry.
- Document site progress and escalate risks or issues to the clinical team.
- Assist in tracking site budgets and ensure timely site payments; collaborate with cross-functional partners (CTAs, LTMs, CTMs). What We're Looking For
- Bachelor’s degree in Life Sciences or equivalent, or qualified RN.
- Eligible to work in the United States without visa sponsorship.
- 2+ years of on-site monitoring experience in the pharmaceutical or CRO industry.
- Experience monitoring early development Phase I/II trials across multiple therapeutic areas.
- Proficient in ICH-GCP, local regulatory requirements, and clinical systems like CTMS and eTMF.
- Clear communicator, problem-solver, and collaborative team player.
- Willing and able to travel up to 60% for on-site monitoring visits; preference for candidates residing near major HUB airports. Compensation & Benefits
- Competitive salary.
- Various annual leave entitlements.
- A range of health insurance offerings to suit you and your family’s needs.
- Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.
- Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family’s well-being.
- Life assurance.
- Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others.
- Visit our careers site to read more about the benefits ICON offers.