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Line Head, Tmf Central Upload And Quality Review

Bristol Myers Squibb
5-7 years
20-30 lakhs
Hyderabad
10 June 15, 2026
Job Description
Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills:

Role Overview

This is a supervisory role responsible for leading a team of eTMF Specialists who manage the upload, review, and quality control of clinical trial documents within the Electronic Trial Master File (eTMF). The position ensures inspection readiness, regulatory compliance, and high-quality document management across BMS clinical trials.


Key Responsibilities

Team Leadership & Resource Management

  • Manage and allocate work across eTMF Specialists.

  • Ensure adequate support for clinical trial priorities.

  • Conduct hiring, performance reviews, coaching, and employee development.

  • Monitor training compliance and team productivity.

eTMF Upload & Quality Review

  • Oversee document upload activities within the eTMF system.

  • Ensure documents meet quality standards and regulatory requirements.

  • Maintain inspection-ready Trial Master Files.

  • Verify correct application of metadata, attributes, and workflows.

Compliance & Regulatory Oversight

  • Ensure adherence to:

    • ICH-GCP Guidelines

    • ALCOA+ Principles

    • Health Authority Requirements

    • Company SOPs and Directives

  • Identify and resolve TMF compliance gaps.

Training & Stakeholder Management

  • Train and mentor team members on TMF processes.

  • Collaborate with Clinical Operations and other stakeholders.

  • Support issue resolution and continuous process improvement initiatives.

Reporting & Analytics

  • Review quality metrics, dashboards, and KPIs.

  • Analyze trends and implement corrective actions.

  • Generate reports using Power BI, Excel, and SharePoint.


Required Qualifications

Education

  • Bachelor's degree in Life Sciences, Pharmacy, Biotechnology, Clinical Research, or related field.

Experience

  • 5–7+ years of experience in:

    • Clinical Trial Documentation

    • eTMF Management

    • Clinical Operations

    • Regulatory Documentation

  • Prior experience managing or supervising teams.

Technical Skills

  • Strong knowledge of:

    • eTMF principles

    • Trial Master File management

    • Clinical document lifecycle

  • Preferred experience with:

    • Veeva Vault eTMF

    • Microsoft Excel

    • Power BI

    • SharePoint

    • PowerPoint

Regulatory Knowledge

  • ICH-GCP

  • ALCOA+

  • Clinical trial regulations

  • TMF Reference Model

  • Inspection readiness requirements


Key Competencies

  • Leadership & Team Management

  • Stakeholder Communication

  • Quality Management

  • Regulatory Compliance

  • Process Improvement

  • Problem Solving

  • Training & Coaching

  • Analytical Thinking

Additional benefits may include:

  • Annual bonus

  • Health insurance

  • Provident Fund

  • Learning & development programs

  • Hybrid work flexibility

  • Employee wellness benefits


Ideal Candidate Profile

A professional with strong TMF/eTMF management experience, expertise in Veeva Vault, regulatory knowledge, and proven people management skills who can lead document quality and compliance activities across global clinical trials while maintaining inspection readiness.