Welcome Back

Google icon Sign in with Google
OR
I agree to abide by Pharmadaily Terms of Service and its Privacy Policy

Create Account

Google icon Sign up with Google
OR
By signing up, you agree to our Terms of Service and Privacy Policy
Instagram
youtube
Facebook

Senior Manager, Clinical Data Standards & Reporting Engineer

Bristol Myers Squibb
8-11 years
Not Disclosed
Hyderabad
1 June 2, 2026
Job Description
Job Type: Full Time Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences Skills: Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding

Senior Manager – Clinical Data Standards & Reporting Engineer

Location: Hyderabad, Telangana, India
Job Type: Full-Time
Company: Bristol Myers Squibb

Position Summary

The Senior Manager, Clinical Data Standards & Reporting Engineer plays a critical role in developing, maintaining, and governing global clinical data standards across the clinical development lifecycle. This position ensures compliance with regulatory requirements, industry standards, and internal frameworks to support successful clinical trial execution and regulatory submissions.

The role serves as a subject matter expert (SME) for clinical data standards, metadata management, CDISC implementation, submission readiness, and reporting standards while collaborating with cross-functional teams across Clinical Operations, Data Management, Biostatistics, Programming, and Regulatory Affairs.


Key Responsibilities

1. Clinical Study & Project Support

Standards Consultation & Guidance

  • Serve as the primary standards SME for study teams regarding the development and implementation of clinical data standards.

  • Provide expert guidance to:

    • Clinical Scientists for protocol standards.

    • Database Developers for data collection standards.

    • SDTM Programmers for SDTM implementation.

    • Statistical Programmers for ADaM datasets and TLF standards.

  • Support study teams in applying end-to-end standards throughout the clinical trial lifecycle.

Regulatory Compliance Support

  • Ensure compliance with:

    • CDISC standards

    • Regulatory submission requirements

    • Internal BMS standards and governance frameworks

  • Provide consultation on validation of CDISC-compliant submission packages and supporting documentation.

Cross-Functional Collaboration

  • Participate in study team and submission team meetings as a Standards SME.

  • Communicate standards interpretation, rationale, and implementation guidance across projects.

  • Promote consistency in standards adoption and execution across clinical programs.

Change Management & Governance

  • Evaluate and process requests for new or updated clinical metadata standards.

  • Develop recommendations and implementation strategies for standards updates.

  • Facilitate approval through established standards governance processes.


2. Global & Therapeutic Area (TA) Standards Development

Clinical Standards Development

  • Contribute to the creation, enhancement, and maintenance of:

    • Protocol standards

    • Data collection standards

    • SDTM standards

    • ADaM standards

    • Analysis and reporting standards

Metadata Management

  • Develop and maintain global and TA-specific metadata repositories including:

    • Protocol metadata

    • CRF standards

    • Non-CRF data standards

    • SDTM mappings

    • Controlled terminology

    • Analysis standards

Submission Standards

  • Create and maintain regulatory submission assets including:

    • Define.xml

    • Annotated CRF (aCRF)

    • Study Data Reviewer’s Guide (SDRG)

    • Analysis Data Reviewer’s Guide (ADRG)

Standards Harmonization

  • Support alignment across:

    • Clinical Development

    • Biometrics

    • Data Management

    • Biostatistics

    • Regulatory Affairs


Technical & Regulatory Expertise

Clinical Data Standards

  • CDISC CDASH

  • SDTM (Study Data Tabulation Model)

  • ADaM (Analysis Data Model)

  • Controlled Terminology

  • Metadata Standards

  • Clinical Trial Data Collection Standards

Regulatory Submission Standards

  • Define.xml

  • aCRF

  • SDRG

  • ADRG

  • FDA Submission Requirements

  • Global Regulatory Guidelines

Reporting & Analytics

  • TLF (Tables, Listings & Figures)

  • Clinical Reporting Standards

  • Submission Package Validation

  • Data Quality & Compliance Monitoring


Required Skills & Competencies

Technical Skills

  • Strong knowledge of CDISC standards (CDASH, SDTM, ADaM).

  • Expertise in clinical trial data standards and metadata management.

  • Understanding of regulatory submission requirements.

  • Experience with Define.xml and reviewer guides.

  • Knowledge of clinical data lifecycle and submission processes.

Soft Skills

  • Stakeholder management.

  • Cross-functional collaboration.

  • Problem-solving and analytical thinking.

  • Standards governance and change management.

  • Strong communication and presentation skills.