Eli Lilly and Company Hiring Associate – Clinical Data Sciences (CDS)

Eli Lilly and Company

Bengaluru

Hybrid

INR 600,000 - 1,200,000

Full time

14 days+
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Benefits offered by this job

Healthcare
Performance bonuses
Global career development

Job summary

Eli Lilly and Company in Bangalore invites expressions of interest for an Associate – Clinical Data Sciences (CDS). You will manage clinical data across global trials, ensuring integrity and regulatory readiness, while collaborating with biostatistics, programming, and operations teams.

Ideal candidates hold a Life Sciences or IT background with strong knowledge of CDISC standards, EDC systems, and data visualization tools. Hybrid work option available in Bangalore, India.

Qualifications

  • Bachelor’s degree in Life Sciences, Pharmacy, Statistics/Informatics or IT.
  • Knowledge of CDISC/SDTM data models and GCP standards.

Responsibilities

  • Execute data management deliverables for global clinical trials.
  • Collaborate with cross-functional teams to ensure data quality and regulatory compliance.
  • Manage data flow across vendors and systems.

Skills

CDISC/SDTM
EDC systems
Data validation
Programming
Data visualization
Analytical mindset
Cross-functional collaboration

Education

Life Sciences (Biotechnology, Microbiology, Biochemistry)
Pharmacy (B.Pharm, M.Pharm)
Statistics / Informatics / Health Information Administration
Information Technology / Nursing / Biomedical Engineering

Tools

Medidata Rave
Inform
Oracle Clinical

Job description

Associate – CDS Vacancy for Life Sciences Graduates | Lilly Bangalore

Join one of the world’s most respected healthcare innovators — Eli Lilly and Company — as an Associate – Clinical Data Sciences (CDS) in Bangalore. This full-time opportunity in the Research & Development (R&D) division allows you to be part of a team dedicated to transforming lives through science, technology, and compassionate healthcare.

As a Clinical Data Management Associate, you will play a key role in ensuring the accuracy, reliability, and integrity of clinical data across global clinical trials. This position combines technical excellence, data analytics, and regulatory understanding — ideal for professionals passionate about clinical research, data integrity, and pharma innovation.

Company Overview

Eli Lilly and Company, headquartered in Indianapolis, Indiana (USA), is a global leader in healthcare innovation with a mission to make life better for people around the world. With over 145 years of scientific excellence, Lilly has transformed modern medicine through its pioneering work in oncology, diabetes, immunology, and neuroscience.

Lilly’s operations in Bangalore, India, focus on data sciences, clinical operations, and R&D support, driving innovation through advanced data management and technology solutions.

The company stands by its values of integrity, excellence, and respect for people, ensuring every medicine developed reflects a commitment to ethical research and global health improvement.

Job Role & Responsibilities

As an Associate – Clinical Data Sciences (CDS), your primary responsibility will be to execute data management deliverables for global clinical trials. You will collaborate with cross-functional teams to ensure database design, data collection, validation, and delivery meet the highest quality and compliance standards.

Key Responsibilities:
  • Manage end-to-end clinical trial data — from setup to final database lock.
  • Implement business requirements and ensure timely delivery of quality datasets.
  • Oversee data flow across multiple vendors, sources, and systems.
  • Contribute to the Data Management Plan, Project Plan, and dataset specifications.
  • Ensure data integrity, adherence to SOPs, and compliance with ICH-GCP, FDA, and MHRA standards.
  • Facilitate integration of niche and complex data sources (PK, biomarker, immunogenicity, etc.).
  • Support submission-ready dataset generation for regulatory purposes.
  • Conduct data validation, review, and query management activities.
  • Participate in regulatory audits and inspection readiness activities.
  • Collaborate with teams on data archiving, standardization, and decommissioning processes.
Project Management Responsibilities:
  • Track progress and report study build, data flow, and delivery metrics.
  • Apply therapeutic area knowledge to improve data review efficiency.
  • Drive operational excellence through continuous process improvement.
  • Ensure compliance with internal and external audit requirements.
Leadership & Collaboration:
  • Represent the Data & Analytics team in cross-functional initiatives.
  • Share learnings and best practices across global data management teams.
  • Promote process improvement to reduce cycle times and enhance quality.
Eligibility / Qualifications

Educational Requirements:

  • Bachelor’s degree in any of the following disciplines:
    • Life Sciences (Biotechnology, Microbiology, Biochemistry)
    • Pharmacy (B.Pharm, M.Pharm)
    • Statistics / Informatics / Health Information Administration
    • Information Technology / Nursing / Biomedical Engineering

Work Location: Bangalore, Karnataka, India
Experience Level: Entry to Mid-Level (Clinical Data Management / Clinical Research background preferred)

Preferred Skills and Competencies
  • Sound understanding of clinical data standards, CDISC, SDTM, and EDC systems (e.g., Medidata Rave, Inform, Oracle Clinical).
  • Knowledge of Good Clinical Practice (GCP) and global regulatory frameworks (FDA, ICH, EMA).
  • Proficiency in data validation, programming, and data visualization tools.
  • Strong analytical mindset and attention to detail.
  • Excellent communication and cross-functional collaboration skills.
  • Proactive problem-solving and critical thinking abilities.
Location & Salary
  • Location: Bangalore, Karnataka, India
  • Department: Research & Development – Clinical Data Sciences
  • Job Type: Full-Time, Regular
  • Compensation: Competitive salary with comprehensive benefits including healthcare, performance bonuses, and global career development opportunities.
Why Join Lilly?
  • Be part of a global pharma leader advancing medical innovation.
  • Collaborate with world-class scientists and data professionals.
  • Work in a diverse, inclusive, and growth-oriented culture.
  • Access to global learning programs, certifications, and mentorship.
  • Contribute to groundbreaking discoveries that improve patient outcomes.
FAQs

Q1: Who can apply for the Associate – CDS position at Lilly?
Graduates in Life Sciences, Pharmacy, Statistics, or Information Technology can apply.

Q2: Is prior experience mandatory?
Not mandatory. Freshers with relevant academic backgrounds or internships in data management are encouraged to apply.

Q3: What tools and systems are used in this role?
Lilly uses global EDC systems like Medidata Rave and Oracle Clinical along with CDISC/SDTM data models.

Q4: What kind of projects will I work on?
You will support global clinical trials in multiple therapeutic areas — Oncology, Immunology, and Endocrinology.

Q5: Is the role remote or on-site?
The position is based at Lilly’s Bangalore office with flexible hybrid working options.

Q6: What are the career growth opportunities?
Lilly offers structured career progression into data leadership, clinical programming, and analytics domains.

Summary
  • Company: Eli Lilly and Company
  • Vacancy: Associate – Clinical Data Sciences (CDS)
  • Required Education: Life Sciences, Pharmacy, IT, Statistics, Informatics
  • Experience: Entry to Mid-Level
  • Location: Bangalore, Karnataka, India
  • Department: Research & Development
  • Job Type: Full-Time, Regular
  • Apply Link: Apply Here
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