Job description

Role overview

This contract opportunity is for a Clinical Research Associate to support a transplant-focused study across the United States, with primary coverage on the West Coast. The assignment is set for 1 year with the possibility of renewal, and the expected start is ASAP. The position is a full-time equivalent role at 1.0 FTE.

What you'll do

Carry out site initiation, routine monitoring, and close-out activities in line with the study schedule; visits are expected about every 6 weeks on average, though the cadence may differ by site.
Verify that participating sites follow the protocol, Good Clinical Practice standards, and all relevant regulatory requirements.
Partner with site personnel to help drive enrollment, improve data quality, and strengthen overall site execution.
Prepare and keep accurate study records, including documentation and monitoring reports, in a timely manner.

Requirements

A bachelor’s degree in a scientific field or a health-related area.
3 to 5 years of experience working as a CRA, ideally in transplant or nephrology research.
Solid knowledge of GCP and ICH guidelines.
Strong communication, planning, and problem-solving abilities.
Readiness to travel to trial sites as needed, including Washington, California, Colorado, and other U.S. locations.

Additional details

This role is intended for a transplant study and requires relevant background in transplant or nephrology trials. Travel across the United States will be part of the job, with a West Coast emphasis. Candidates should be prepared for an immediate start.

Application note

Applications are requested as soon as possible because the submission window is limited.

Contract Clinical Research Associate