Job Summary
A company is looking for a Clinical Trial Associate to coordinate activities on clinical research projects.
Key Responsibilities
- Draft project plans and create project documents for review
- Act as a central contact for project communications and meeting coordination
- Maintain and update clinical systems and Trial Master Files (TMF) in an audit-ready state
Required Qualifications
- Associate degree in a life science or health-related field required; Bachelor's degree preferred
- Minimum of 4 years of experience in an administrative role
- At least 3 years of experience in support of clinical research, preferably in oncology
- Experience managing Trial Master Files and/or Investigative Site Files
- Proficiency with Microsoft Office applications
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