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Benefits offered by this job
Medical insurance
Vision insurance
401(k) benefits
Job summary
A biotechnology organization is seeking a skilled Clinical Trial Associate to join their innovative team remotely. The ideal candidate will have over 3 years of experience in clinical trial coordination and documentation management. This full-time contract position involves managing study start-up tasks, Trial Master Files, and maintaining communication with study teams. Strong organizational and communication skills are required, with preferred proficiency in Veeva Vault and Microsoft Office.
Qualifications
3+ years of experience as a Clinical Trial Associate.
Proven experience with study start-up and TMF management.
Coordinate study start-up tasks and documentation.
Manage Trial Master Files and Investigator Site Files.
Prepare study materials and maintain contact lists.
Skills
Clinical trial coordination
Documentation management
Budget tracking
Communication
Detail-oriented
Tools
Veeva Vault eTMF
Microsoft Word
Microsoft Excel
Microsoft PowerPoint
Job description
A biotechnology organization is seeking a skilled Clinical Trial Associate to join their innovative team remotely. The ideal candidate will have over 3 years of experience in clinical trial coordination and documentation management. This full-time contract position involves managing study start-up tasks, Trial Master Files, and maintaining communication with study teams. Strong organizational and communication skills are required, with preferred proficiency in Veeva Vault and Microsoft Office.