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Etmf Specialist

Novotech
NovoTech
3+ years
Not Disclosed
India
10 March 19, 2026
Job Description
Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

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.