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Senior Associate-Clinical Operations

Elanco
2+ years
INR 8 LPA – 12 LPA
Bangalore, India
1 June 10, 2026
Job Description
Job Type: Full Time Education: M.Pharm/B.Pharm or M.Sc. Skills: Medical Coding, Medical Terminology, mRS and EQ-5D-5L., Narrative Writing

Senior Associate – Clinical Operations (R&D Quality Systems & Global Training)

Location: Bengaluru, India
Employment Type: Full-Time
Company: Elanco
Experience Required: 2+ Years
Travel Requirement: Up to 5%


About Elanco

At Elanco, innovation starts with animals. As a global leader in animal health, Elanco develops products and services that help prevent and treat diseases in farm animals and pets. The company is committed to improving animal welfare while supporting customers, communities, and employees worldwide.


Position Overview

The Specialist, R&D Quality Systems & Global Training is responsible for independently managing and supporting Elanco’s global R&D quality and training framework. The role focuses on Quality Management Systems (QMS), training compliance, document control, compliance reporting, and data-driven process improvement.

The ideal candidate should possess strong knowledge of regulated environments, quality systems, training management, and compliance processes while effectively collaborating with global stakeholders.


Key Responsibilities

1. Quality Management System (QMS) Operations

  • Manage R&D Quality Management System activities independently.

  • Monitor quality metrics, document tracking, and compliance reporting.

  • Support continuous improvement initiatives across quality processes.

  • Maintain accurate quality records and documentation.

2. Global Training Management

  • Execute global R&D training programs.

  • Ensure the right training is assigned to the right employee at the right time.

  • Monitor training completion and compliance status.

  • Support training audits and compliance reviews.

3. Data Analytics & Reporting

  • Utilize Power BI for compliance dashboards and reporting.

  • Analyze quality and training data to identify trends and compliance gaps.

  • Generate management reports and visualizations.

  • Leverage AI-based tools to improve productivity and reporting efficiency.

4. Documentation & Process Support

  • Create, update, and maintain SOPs, job aids, and procedural documents.

  • Ensure document accuracy and regulatory compliance.

  • Maintain document lifecycle management within electronic systems.

5. System Administration

  • Act as a key user for:

    • Veeva Quality Vault

    • SuccessFactors LMS

    • Microsoft Office Applications

    • Adobe Acrobat

  • Support system-related troubleshooting and user guidance.

6. Compliance & Audit Support

  • Assist during regulatory inspections and internal audits.

  • Provide complete and accurate documentation.

  • Support corrective and preventive actions where applicable.

  • Ensure inspection readiness across quality processes.

7. Metrics & Compliance Monitoring

  • Update compliance dashboards and reports.

  • Track training and quality performance indicators.

  • Communicate compliance status to stakeholders and management.


Leadership & Collaboration Responsibilities

Cross-Functional Coordination

  • Collaborate with R&D, Regulatory Affairs, and Quality teams globally.

  • Build effective relationships with internal and external stakeholders.

Independent Decision-Making

  • Prioritize tasks effectively with minimal supervision.

  • Resolve routine operational challenges independently.

  • Escalate critical issues when necessary.

Operational Excellence

  • Deliver high-quality work within established timelines.

  • Maintain accuracy in documentation and compliance activities.

  • Contribute to process improvement initiatives.

Adaptability

  • Support evolving business priorities and system implementations.

  • Demonstrate flexibility in a dynamic global environment.


Required Qualifications

Education

  • Bachelor's Degree in:

    • Life Sciences

    • Pharmacy

    • Biotechnology

    • Scientific Discipline

    • Business Administration

    • Related Field

Experience

  • Minimum 2 years of experience in:

    • Quality Systems

    • Document Management

    • Clinical Operations Support

    • Training Compliance

    • Regulated Environments