Adecco India is hiring for a TMF Co-Ordinator job in Bangalore on a 12-month contract. This role is ideal for candidates with experience in clinical operations, eTMF (electronic Trial Master File), and clinical document management. The position sits under Quality Assurance and focuses on ensuring ICH GCP compliance, regulatory documentation accuracy, and clinical trial documentation control.
This TMF Co-Ordinator job in Bangalore offers an excellent opportunity to work in global clinical research environments and build expertise in eTMF systems and clinical quality documentation.
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Key Responsibilities โ TMF Co-Ordinator Job Bangalore
As part of this TMF Co-Ordinator job in Bangalore, you will:
- Manage and maintain clinical trial master files (TMF/eTMF)
- Ensure accurate filing, indexing, and tracking of clinical documents
- Support compliance with ICH GCP guidelines and regulatory requirements
- Coordinate with clinical operations teams for document completeness
- Perform quality checks for TMF completeness and audit readiness
- Maintain inspection-ready documentation at all times
- Support quality assurance activities within clinical trials
- Handle electronic and paper-based clinical documentation workflows
Eligibility & Qualifications
To apply for this TMF Co-Ordinator job in Bangalore, candidates should have:
- Bachelorโs degree in Life Sciences, Pharmacy, Healthcare, or related field
- 1โ4 years of experience in clinical operations or clinical document management
- Strong understanding of eTMF systems and clinical research documentation
- Knowledge of ICH GCP and regulatory compliance frameworks
- Proficiency in MS Office (Word, Excel, etc.)
- Good communication and documentation skills
Skills Required
- TMF / eTMF management
- Clinical document control
- ICH GCP compliance
- Clinical operations support
- Regulatory documentation handling
- Quality assurance processes
Salary Details
- โน7,00,000 โ โน8,00,000 per annum (approx.)
- Contract-based role (12 months)
Benefits of This TMF Co-Ordinator Job in Bangalore
- Exposure to global clinical trial documentation systems
- Hands-on experience with eTMF platforms and QA processes
- Opportunity to work with a leading staffing and consulting group
- Strong career growth in clinical research and quality assurance
- Industry-relevant experience in regulated environments
How to Apply
