Assist CRAs and RSU team with accurately updating and maintaining clinical documents and systems (e.g., Trial Master File (TMF)) that track site compliance and performance within project timelines
Job Summary
Assist CRAs and RSU team with accurately updating and maintaining clinical documents and systems (e.g., Trial Master File (TMF)) that track site compliance and performance within project timelines.
Assist the clinical team with the preparation, handling, distribution, filing, and archiving of clinical documentation and reports according to the scope of work and standard operating procedures.
Act as a central contact for the clinical team for designated project communications, correspondence and associated documentation.
Matching Summary
Assist CRAs and RSU team with accurately updating and maintaining clinical documents and systems (e.g., Trial Master File (TMF)) that track site compliance and performance within project timelines.
Skills & Requirements
Must-have
Clinical document management
Trial Master File (TMF) maintenance
Regulatory and Start-Up (RSU) support
Clinical documentation handling
Clinical data flow tracking
Nice-to-have
Effective time management
Organizational skills
Establish working relationships
Key Requirements
Bachelors Degree in Pharmaceutical or related field