Clinical Site Associate

Job Summary

Supporting clinical trial operations, the remote Clinical Site Associate will manage site communications, maintain documentation, and ensure site compliance while collaborating with cross-functional teams.

Key responsibilities

• Manage site-level communications and coordinate site trainings and access
• Support site readiness activities, including pre/post site visit tasks and follow-up on action items
• Maintain the Trial Master File (TMF) to ensure accurate documentation

Required qualifications

• Bachelor's degree in a relevant field such as Life Sciences or Healthcare
• Minimum of one year of experience as a Study Coordinator in clinical research
• Previous experience in clinical research or a related field preferred
• Strong organizational skills and ability to prioritize tasks effectively
• Ability to work independently and collaboratively in a fast-paced environment