Clinical Trial Associate

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