Clinical Trial Specialist II
On-site · Remote, Oregon, United States
Job Summary
Responsible for investigative site recruitment/feasibility, site project training, remote clinical data monitoring and resolution, site progress tracking, in-house site management, documentation filing, and other duties in accordance with Sponsor and/or UBC requirements. Performs essential document collection and review for site start up and initiates in compliance with project specifications and applicable SOPs with adherence to FDA Regulations, ICH/GCP guidelines and good documentation practices. Demonstrates ability to successfully lead and mentor CTS staff, take on high level tasks as delegated by Project Manager/Functional Manager, and escalate and mitigate risk as appropriate.
Required Qualifications
- Bachelor's degree or relevant work experience required
- 2+ years of relevant clinical research experience required
- Excellent written and verbal communication skills required
- Strong Microsoft Office skills (Outlook, Word, Excel) required
- Aptitude in learning new computer systems required
Apply with one swipe on Sorce. We auto-fill applications and apply on your behalf — no cover letters, no 40-minute forms.
Hiring someone like this?
Get your role in front of qualified candidates on Sorce.