Overview
Skills
Job Details
Please note that this is a 12 to 18-month contract position.
Notes from the Manager:
It can be fully remote but must work in PST timezone.
For this position, it is more of a specialist role, so their day-to-day won t be typical.
The ideal candidate for this role would have at least 5 years of experience as a CRA and may already have some CTM experience.
It will also help if they have some QA experience.
Clinical coordinators would not work.
Job Posting Qualifications
Bachelor's or Master's Degree or equivalent.
Post-graduate, certification, and/or license may be required.
Typically, at least 3 - 5+ years relevant experience.
Job Posting Description
Responsible for overall clinical study management, including planning, communication, coordination and practical tasks for the studies.
Coordinates Ethical Committee and Institutional Review Board notifications.
Creates, maintains and oversees study files and archiving.
Manages testing laboratories including selection of laboratories for the studies.
Manages clinical research organizations and ensures monitoring of studies, data collection and handling.
Prepares, revises and maintains procedures for the conducting of clinical studies.
Applicants must provide their phone number. Reference job number A4993