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Senior Associate-Clinical Operations

Elanco
2+ years
INR 6 LPA – 10 LPA
Bangalore, India
1 June 12, 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

Company: Elanco
Location: Bangalore, India
Job Type: Full-Time
Department: R&D Quality Systems & Global Training
Experience: 2+ Years

About the Role

Elanco is seeking a Senior Associate – Clinical Operations to support its R&D Quality Systems and Global Training function. The role involves managing quality management system activities, training compliance, document control, compliance reporting, and supporting global regulatory requirements across R&D operations.

The ideal candidate will have experience in quality systems, document management, training administration, and regulated environments, with the ability to work independently while collaborating with global stakeholders.

Key Responsibilities

Quality Management System (QMS) Operations

  • Manage R&D Quality Management System activities including:

    • Metrics collection

    • Document tracking

    • Compliance monitoring

    • Status reporting

  • Support global quality and compliance initiatives.

  • Ensure adherence to internal procedures and regulatory requirements.

Training & Compliance Management

  • Execute Global Quality System training programs.

  • Ensure appropriate training assignment, completion, and compliance tracking.

  • Maintain training records and support training effectiveness initiatives.

Data Analytics & Reporting

  • Utilize Power BI to generate compliance dashboards and reports.

  • Analyze compliance trends and identify process improvement opportunities.

  • Support data visualization and reporting activities for R&D leadership.

Documentation & Process Support

  • Author and maintain:

    • Job Aids

    • Standard Operating Documents

    • Process Documentation

    • Working Instructions

  • Ensure documentation accuracy, consistency, and compliance.

System Administration

  • Support and maintain R&D systems including:

    • Veeva Quality Vault

    • SuccessFactors

    • MS Office Applications

    • Adobe Acrobat

  • Act as a key user for quality and training-related systems.

Compliance & Audit Support

  • Support regulatory inspections and internal audits.

  • Provide required documentation and compliance reports.

  • Assist with audit readiness and corrective action activities.

Leadership & Collaboration Responsibilities

  • Collaborate with stakeholders across R&D, Regulatory Affairs, and Quality functions.

  • Proactively identify process issues and recommend solutions.

  • Support cross-functional initiatives and continuous improvement projects.

  • Deliver objectives in a timely, high-quality, and cost-effective manner.

  • Demonstrate adaptability in a dynamic and evolving work environment.

Required Qualifications

Education

  • Bachelor's Degree in:

    • Life Sciences

    • Pharmacy

    • Biotechnology

    • Business Administration

    • Related Scientific Discipline

Experience

  • Minimum 2+ years of experience in:

    • Quality Systems

    • Document Management

    • Clinical Operations Support

    • Regulatory Compliance

    • Regulated Environments

  • High-potential candidates with 1–2 years of relevant experience may also be considered.

Required Skills

  • Quality Management Systems (QMS)

  • Document Management

  • Regulatory Compliance

  • Clinical Operations Support

  • Training Administration

  • Veeva Vault

  • SuccessFactors LMS

  • Power BI

  • Compliance Reporting

  • Audit & Inspection Readiness

  • Data Analysis & Visualization

  • SOP Management

  • Stakeholder Management

  • Cross-Functional Collaboration

  • Problem Solving

  • Communication Skills