Clinical Trial Associate (CTA) & TMF Specialist
Easy apply
New
Job summary
Support Clinical Trial execution while ensuring regulatory compliance and maintaining an inspection-ready Trial Master File (TMF).
Min Qualification:
MBBS
Experience Level:
Entry level
Experience Length:
2 years
Working Hours:
Full Time
Job descriptions & requirements
Responsibilities:
- Support clinical trial execution while ensuring regulatory compliance and maintaining an inspection-ready Trial Master File (TMF).
- Clinical trial operations support.
- TMF management & document control.
- Regulatory documentation & compliance tracking.
- Study start-up and coordination support.
- Inspection readiness & audit support.
Requirements:
- 2–4 years of clinical research experience.
- TMF management experience (CRO or sponsor preferred).
- Strong understanding of ICH-GCP and clinical documentation standards.
- Experience supporting Phase I–IV trials preferred.
Important safety tips
- Do not make any payment without confirming with the Jobberman Customer Support Team.
- If you think this advert is not genuine, please report it via the Report Job link below.
