About the role
- Responsible for performing activities in compliance with applicable Corporate and Clinical Operations Policies
- Assists Clinical Monitoring staff with site management activities
- Communicating with sites to ensure compliance with protocol requirements
- Creates and assists with the maintenance of Trial Master File (TMF) and project files
- Prepares and maintains site manuals, reference tools and other documents
- Maintains, updates, and inputs clinical tracking information into databases
- Tracks incoming and outgoing clinical and regulatory documents
- Manages shared mailbox, processes site requests and routes correspondence appropriately
- Assists with coordination of team meetings, attends meetings and prepares accurate meeting minutes and action items
- Maintains overall awareness in the field of clinical research by completing all necessary and assigned training
Requirements
- High School diploma or equivalent
- Good communication and interpersonal skills
- Ability to embrace new technologies
- Minimal travel up to 25% may be required
- supportive and engaged line management
- technical and therapeutic area training
- peer recognition and total rewards program
Applicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Soft skills
communication skillsinterpersonal skills
Certifications
High School diploma