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Associate Director- Clinical Data Standards

0-2 years
Not Disclosed
10 Feb. 13, 2025
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

Job Title: Associate Director - Clinical Data Standards
Job ID: REQ-10022081
Location: Mumbai, India (Alternate Location: Hyderabad, India)
Division: Development
Business Unit: Innovative Medicines
Functional Area: Research & Development
Employment Type: Full-time, Regular
Company / Legal Entity: Novartis Healthcare Private Limited


Role Overview

The Associate Director - Clinical Data Standards will support the Director of Clinical Data Standards by advising and leading the development, planning, and implementation of clinical data standards and technologies that are compliant with industry (CDISC) and regulatory guidelines. This role is responsible for ensuring high-quality data standards in clinical trials, automation technologies, and maintaining global alignment. It involves supporting internal teams, providing expert advice, and overseeing the technical and strategic aspects of clinical data standards. You will also contribute to business infrastructure and guideline development.


Key Responsibilities

  • Data Standards & Automation Solutions:
    Oversee the planning, development, validation, and support of clinical data standards and automation solutions that align with CDS strategies and compliance needs.

  • Global Data Standards Leadership:
    Act as the primary point of contact for global/therapeutic area (TA) data standards. Ensure timely and quality deliverables in alignment with business requirements.

  • Governance & Compliance:
    Lead efficient governance and approval processes for global clinical data standards. Ensure regulatory and industry standards are met, and liaise with governance boards as necessary.

  • Standardization & Impact Analysis:
    Lead the review and assessment of industry and regulatory standards. Perform gap analysis and develop action plans for their implementation.

  • Subject Matter Expert (SME):
    Provide expert consultation, training, and technical support for the implementation of standards and tools across clinical development programs. Act as the SME for various systems, including EDC, edit check programming, TFLs, and metadata management.

  • Mentoring & Leadership:
    Mentor and provide technical guidance to Clinical Data Standards associates. Contribute to talent development and support the growth of the team.

  • Cross-Functional Collaboration:
    Work across departments (e.g., database programming, clinical trials, data analytics) to implement standards in clinical development and regulatory processes.


Key Performance Indicators

  • Timely Execution: Ensure the timely execution of projects and data requests.
  • Stakeholder Feedback: Regular feedback from project sponsors and key stakeholders regarding data standardization processes.
  • Adherence to Policies: Ensure adherence to Novartis policies, guidelines, and KPIs.

What You’ll Bring to the Role

  • Experience & Skills:

    • Strong background in Clinical Data Standards, clinical trials, and data analytics.
    • Proven experience in automation solutions, metadata management, and statistical analysis.
    • Ability to work with cross-functional teams and represent Novartis across boundaries.
    • Project management and decision-making skills to ensure effective planning and execution of clinical data standardization initiatives.
  • Technical Expertise:

    • Expertise in clinical trials, biostatistics, and data standards implementation.
    • Familiarity with relevant industry standards such as CDISC and regulatory requirements.
  • Communication:

    • Strong influencing and presentation skills with proficiency in English.

Why Novartis?

Novartis is a global leader in improving patient outcomes, driven by science, collaboration, and passion. The company offers an opportunity to be part of a community focused on breakthroughs that change patients’ lives.

For more details on Benefits & Rewards and People & Culture, visit their career site.


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