legendcareers
Senior Clinical Trial Associate (Contractor)
At a Glance
- Location
- United States
- Work Regime
- remote
- Experience
- 3–5 years
- Posted
- 2026-03-19T16:36:23-04:00
Key Requirements
Required Skills
Domain Knowledge
- Biotech
- Clinical
- Regulatory
Requirements
Minimum of 3–5 years of experience as a Clinical Trial Associate or in a similar clinical research role.
Demonstrated experience supporting trial coordination, regulatory documentation, and site management activities.
Proficiency with CTMS, eTMF, and EDC systems.
Responsibilities
CTA) to join our growing Clinical Operations team to support early-stage clinical development.
CTA will play a critical role in the execution of complex Phase I/II CAR-T oncology clinical trials by providing high-quality operational, administrative, and coordination support.
The ideal candidate will have substantial experience in clinical trial operations and administration, with a strong understanding of clinical trial processes, regulatory requirements, and GCP.
This role is critical to ensuring the efficient execution of clinical trials, maintaining regulatory compliance, and providing operational support to cross-functional study teams.
Clinical Trial Operations Support
Provide cross-functional administrative and operational support for study team meetings, advisory boards, investigator meetings, and other study-related forums.
About the Company
For information related to our privacy notice, please review:
Legend Biotech Privacy Notice
.