A pharmaceutical company is actively seeking a new Clinical Trial Associate to provide essential support for clinical trial teams, ensuring compliance with regulations and standard procedures.

Responsibilities:
- Performing administrative tasks to support trial execution, including document management and meeting coordination
- Filing study documents, maintaining essential documents lists, and participating in TMF completeness reviews
- Tracking and maintaining study-specific information and dashboards
- Supporting communication and information tracking between study teams, sites, and vendors
- Assisting with vendor management
- Performing other duties, as needed
Qualifications:
- Bachelor's Degree
- Computer-savvy, including the ability to use databases and spreadsheets.
- Solid analytical and problem-solving skills
- Great interpersonal and communication skills
- Strong attention to detail
Desired Qualifications:
- 1+ year of experience in Clinical Trials
- Bachelor's Degree in a Health and/or Science-related field
- Previous experience in a Research role/environment
- Experience with electronic Trial Master File (eTMF) systems
