Clinical Research Associate II

ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.

- 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

- Assist in tracking site budgets and ensuring timely site payments (as applicable)

- Collaborate with cross-functional partners including CTAs, LTMs, and CTMs

- A graduate with a Bachelor's degree in Life Sciences or equivalent, or a qualified RN

- Eligible to work in United States without visa sponsorship

- A clinical research professional with 2+ years of on-site monitoring experience in the pharmaceutical or CRO industry

- Experienced monitoring Oncology (i.e. Prostate Cancer, and Lung Cancer) and/or Hematology oncology.

- Proficient 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 in Los Angeles, Phoenix, Seattle, Denver or Portland, n ear major HUB airports to support efficient regional travel