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

Advisor Gdm

Elanco
10+ years
₹25 – ₹45 LPA
Bangalore, India
15 July 20, 2026
Job Description
Job Type: Full Time, Hybrid, Remote Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Regulatory Affairs, Regulatory Writing, Regulatory Compliance, Global Submissions, eCTD, IND/NDA/BLA Submissions, ICH-GCP, Regulatory Strategy, Regulatory Intelligence, Labeling Strategy.

Advisor – Global Data Management (GDM) | Elanco

Job Details

  • Job Title: Advisor – Global Data Management (GDM)

  • Company: Elanco

  • Job ID (Req ID): R0024897

  • Location: Bangalore, Karnataka, India

  • Job Type: Full-time

  • Department: Global Data Management / R&D

  • Experience Required: 10+ years

  • Travel Requirement: 0%

  • Application Deadline: 21 July 2026

  • Estimated Salary Package (Market Standard): ₹25 – ₹45 LPA (depending on global data management expertise, leadership experience, and industry background)


About the Company

Elanco is a global leader in animal health, focused on developing innovative products and solutions for preventing and treating diseases in farm animals and pets. The company works across global R&D functions to deliver safe and effective animal health products while promoting innovation, collaboration, and scientific excellence.


Job Purpose

The Advisor – Global Data Management (GDM) will provide strategic leadership for global clinical data management activities, ensuring effective data capture, management, reporting, storage, and archival processes. The role involves collaborating with R&D teams, regulatory functions, biostatistics, quality assurance, internal sites, and external partners to ensure data integrity, compliance, and successful delivery of clinical databases.


Key Responsibilities

Global Data Management Leadership

  • Develop and implement global clinical data management strategies.

  • Lead Data Management (DM) activities for clinical projects and internal sites.

  • Ensure timely delivery of final clinical databases.

  • Drive standardization of data management processes across projects and teams.

  • Act as the primary point of contact for assigned DM activities.

Clinical Data Management & Systems

  • Provide expertise in:

    • Electronic Data Capture (EDC) systems.

    • Data management platforms.

    • System deployment, validation, testing, and implementation.

  • Ensure compliance with:

    • GxP regulations.

    • Global data management standards.

    • Clinical data collection and reporting requirements.

  • Support database validation, data quality, and integrity processes.

Study Data Management Activities

  • Prepare and implement Study Data Management Plans (DMPs).

  • Maintain project timelines and ensure milestone completion.

  • Review and contribute to data management documents, including:

    • Data Management Plans.

    • Project Plans.

    • User Acceptance Testing (UAT) logs.

    • Edit Check Specifications (EFPs).

    • Training documents.

  • Monitor workload forecasts and project-level resource requirements.

Stakeholder Management

  • Collaborate with:

    • Clinical Development teams.

    • Biostatistics.

    • Regulatory Affairs.

    • Quality Assurance.

    • Internal study sites.

    • External collaborators.

  • Represent Data Management needs across R&D functions.

  • Facilitate communication between global DM teams and project stakeholders.

Training & Mentoring

  • Educate R&D teams on:

    • Data collection processes.

    • DM systems.

    • Industry best practices.

  • Coach and mentor Data Management colleagues.

  • Promote innovation and continuous improvement.


Required Qualifications

  • Bachelor’s degree or equivalent experience in:

    • Information Technology.

    • Statistics.

    • Scientific field related to animal health.

    • Relevant animal drug development experience.

  • 10+ years of experience supporting global networks, preferably in animal health R&D.

  • Strong understanding of clinical data management processes.

  • Experience leading cross-functional teams and global projects.

  • Knowledge of electronic data systems and validation processes.


Preferred Qualifications

  • Clinical trial data management experience.

  • Advanced knowledge of Electronic Data Capture (EDC) systems.

  • Experience with regulatory submissions and regulatory authority interactions.

  • Project management experience.

  • Quality Management System (QMS) development experience.

  • Experience in animal health clinical development.


Preferred Skills

  • Global Clinical Data Management.

  • Electronic Data Capture (EDC).

  • Clinical trial database management.

  • Data validation and compliance.

  • GxP regulations.

  • Regulatory submission support.

  • Study Data Management Plans (DMP).

  • UAT and system validation.

  • Clinical research operations.

  • Project leadership.

  • Stakeholder management.

  • Team mentoring and coaching.


One-Line Experience

Candidates with 10+ years of experience in global clinical data management, EDC systems, clinical trials, and R&D data operations, preferably in animal health or pharmaceutical industries, are preferred.


Salary Package

  • Estimated CTC: ₹25 – ₹45 LPA

  • Experienced Global DM Leaders: ₹35 – ₹50 LPA+ may be possible depending on expertise.

  • Compensation depends on:

    • Global clinical data management experience.

    • Leadership responsibilities.

    • EDC/system expertise.

    • Animal health/pharma R&D background.


Why Join Elanco?

  • Opportunity to lead global clinical data management initiatives.

  • Work with international R&D teams and advanced data systems.

  • Exposure to animal health drug development programs.

  • Leadership role with strategic impact on clinical research operations.

  • Strong career growth opportunities in global data management and clinical development.