Sr. Clinical Research Associate
About the role
ICON plc is a world-leading healthcare intelligence and clinical research organization. We foster an inclusive environment driving innovation and excellence, welcoming you to join our mission to shape the future of clinical development.
Responsibilities
- Serve as the primary point of contact between investigational sites and the sponsor
- Conduct all types of 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, ensuring timely and accurate AE/SAE/PQC reporting
- Support subject recruitment and retention efforts at the site level
- Oversee drug accountability and ensure 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
- Absorb site budgets and ensure timely site payments (as applicable)
- Collaborate with cross-functional partners including CTAs, LTMs, and CTMs
Requirements
- A graduate with a Bachelor’s degree in Life Sciences or equivalent, or a qualified RNE
- At least 3+ years of on-site monitoring experience in the pharmaceutical or CRO industry
- Experience monitoring Oncology specifically Myelofibrosis clinical trials
- Proficiency in ICH-GCP, local regulatory requirements, and clinical systems like CTMS and eTMF
- A clear communicator, problem-solver, and collaborative team player
- Willing and able to travel up to 50% for on-site monitoring visits across the West region; preference given to candidates residing near major HUB airport to support efficient regional travel
Qualifications
ICON is an equal opportunity employer and welcomes applications from all qualified individuals. We are committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.
Benefits
Our benefits are designed to be competitive within each country and are focused on well-being and work-life balance opportunities for you and your family. Benefits examples include various annual leave entitlements, a range of health insurance offerings, competitive retirement planning offerings, and a global Employee Assistance Programme (LifeWorks).
Pay
Salary range: $110,520.00-$138,150.00
Schedule
Not specified