eTMF Specialist – Clinical Trial Documentation & TMF Management
Location: India
Company: Novotech
Employment Type: Full-Time
Job Overview
Novotech is seeking an experienced eTMF Specialist to lead and manage Trial Master File (TMF) activities across clinical trials. This role serves as a subject matter expert (SME) responsible for ensuring that TMFs are compliant with Good Clinical Practice (GCP), regulatory requirements, and internal Standard Operating Procedures (SOPs). The successful candidate will oversee end-to-end TMF lifecycle management, support cross-functional teams, and drive process improvements and system optimization to maintain inspection-ready TMFs.
Key Responsibilities
TMF Strategy & Oversight
Lead TMF strategy, including development and maintenance of TMF SOPs and study-specific processes
Ensure TMF plans are established and implemented for all assigned clinical studies
Act as the primary SME for TMF management and documentation standards
eTMF Management & Compliance
Oversee end-to-end TMF lifecycle including study start-up, maintenance, and close-out
Ensure TMFs are complete, accurate, and continuously inspection-ready
Conduct quality control (QC) and completeness reviews in alignment with GCP and regulatory requirements
Maintain compliance with DIA TMF Reference Model and industry standards
System Management & Innovation
Optimize the use of eTMF systems by implementing automated workflows and best practices
Support system integrations, upgrades, and user access management
Collaborate with vendors for system-related activities and issue resolution
Cross-Functional Collaboration
Partner with Clinical Operations, Quality Assurance (QA), and other stakeholders to ensure TMF compliance
Provide training and guidance to study teams on TMF processes and document filing standards
Support internal teams in accurate and timely document management
Reporting & Continuous Improvement
Generate TMF metrics, compliance reports, and performance dashboards
Identify gaps and drive process improvements to enhance TMF quality and efficiency
Lead or contribute to departmental and organizational improvement initiatives
Governance & Administration
Participate in vendor management, contract oversight, and financial tracking activities
Ensure all TMF-related activities adhere to Novotech policies and regulatory expectations
Represent TMF function in clinical team meetings and audits
Required Qualifications
Bachelor’s degree in Life Sciences, Clinical Research, or a related field
Strong knowledge of clinical trial documentation, GCP guidelines, and TMF processes
In-depth understanding of DIA TMF Reference Model and clinical trial lifecycle
Proficiency in eTMF systems and document management platforms
Excellent organizational, analytical, and communication skills
Experience Required
Minimum 3+ years of experience in TMF management within a CRO, pharmaceutical, or biotech organization
Hands-on experience across study start-up, maintenance, and close-out phases
Proven experience in TMF quality review, compliance, and audit readiness
Key Skills
Trial Master File (TMF) Management
eTMF Systems & Process Optimization
GCP & Regulatory Compliance
Quality Control & Inspection Readiness
Clinical Documentation Standards
Stakeholder Collaboration & Training
Data Analysis & Reporting
Why Join Novotech?
Opportunity to work with a leading global Contract Research Organization (CRO)
Exposure to international clinical trials and advanced digital systems
Inclusive, collaborative, and innovation-driven work culture
Flexible work environment with strong focus on employee wellbeing
Continuous learning, mentorship, and career advancement opportunities
About Novotech
Novotech is a globally recognized full-service CRO delivering clinical development and scientific advisory services to pharmaceutical, biotechnology, and medical device companies. With a strong international presence, Novotech is committed to accelerating clinical innovation and improving patient outcomes worldwide.
How to Apply
Interested candidates can apply via Novotech’s official careers portal or submit their updated resume through ThePharmaDaily.com to explore global clinical research career opportunities.
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