About this role
Job Responsibilities: Assist Clinical Research Associates (CRAs) and Regulatory and Start-Up (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. Assist with periodic review of study files …
What they're looking for
Responsibilities
- •Assist CRAs and RSU team with updating clinical documents and systems
- •Maintain clinical documents and systems (e.g., TMF)
- •Track site compliance and performance within project timelines
- •Assist with preparation, handling, distribution, filing, and archiving of clinical documentation
- •Assist with periodic review of study files
Frequently asked questions
What does a Clinical Trial Assistant at IQVIA do?
Job Responsibilities: Assist Clinical Research Associates (CRAs) and Regulatory and Start-Up (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 tea…
How much does a Clinical Trial Assistant at IQVIA pay?
The employer did not list a salary for this role. Most similar Singapore roles publish their band on the job page.
Is this Clinical Trial Assistant role remote, hybrid, or on-site?
The listing is based in Singapore. Check the posting for remote or hybrid options.
How do I apply for this Clinical Trial Assistant role?
You can apply directly on IQVIA's careers page. ApplyLah can tailor your résumé and cover letter to this exact role in seconds first.