A pharmaceutical company in Massachusetts is currently seeking a new Clinical Trial Associate role to provide essential support to Clinical Trial teams.

About the Opportunity:
- Schedule: Full-time
- Hours: 40 hours/week
Responsibilities:
- Performing administrative tasks to support clinical trial execution, including document management and meeting coordination
- Filing and tracking study documents in electronic systems and coordinating document reviews
- Maintaining the accuracy of study-specific information using databases and spreadsheets
- Supporting communication and tracking between study teams, sites, and vendors
- Helping manage vendor relationships
- Performing other duties, as needed
Qualifications:
- 2+ years of relevant work experience
- Associate's and/or Bachelor's Degree
- Proficiency in Document Management and Database Systems
- Strong organizational skills
- Good interpersonal and communication skills
- Strong attention to detail
- Flexibility and adaptability
Desired Qualifications:
- Bachelor’s Degree in a Healthcare and/or Scientific-related role
- Proficiency in Project Management tools
- Experience in a Research role/setting
