GSK Hiring for Clinical Data System Analyst Role: Pharma Jobs 2026

ByPharma Hiring Hub

GlaxoSmithKline (GSK), a global biopharma leader, is hiring Analysts for its Data Sciences & Management (DS&M) teams in Bengaluru. This role is perfect for candidates interested in clinical data management, EDC systems, ePRO solutions, vendor data integration, and regulatory‑compliant data workflows within the pharmaceutical industry.

As an Analyst, you will support the setup, testing, and maintenance of Electronic Data Capture (EDC) systems, assist with clinical data quality checks, ensure smooth vendor data integration, and contribute to digital health and regulatory‑focused data processes.

Candidates from clinical research, pharmacovigilance, CDM, life sciences analytics, or healthcare data backgrounds will find this opportunity highly aligned with their career goals.

Working at GSK provides exposure to global clinical trial platforms, advanced digital solutions, and industry‑leading compliance standards, all while contributing to innovations that improve patient health worldwide.

Gsk hiring fresher for analyst

Job Overview

  • Position: Analyst- CDS system
  • Department: CDM
  • Location: Bengaluru
  • Experience: 0 to 3 Years
  • Qualification: B.Pharm, M.Pharm, Lifescience Graduate
  • Job Type: Full-Time
  • Last date of application: 12-Mar-2026

Key Responsibilities – Clinical Data System Analyst

  • Develop & Maintain eDC/ePRO Systems: Support the technical setup, development, and maintenance of Electronic Data Capture (eDC) and Electronic Patient‑Reported Outcomes (ePRO) systems, along with vendor data acquisition activities.
  • Automation & Tool Enhancement: Contribute to process automation, assist in tool maintenance, and support development initiatives that improve operational efficiency.
  • Apply Technical Expertise: Use technical skills in areas such as programming, UAT, data cleaning, data analysis, validation, and regulatory submission support as needed.
  • Quality & Compliance Support: Assist with creating and maintaining study‑level quality plans and ensure all trial‑related documentation is accurately filed in the eTMF system.
  • Adhere to SOPs & Training: Follow departmental SOPs, corporate policies, and regulatory guidelines. Complete all training modules via Learning Hub or Instructor‑Led Training (ILT).
  • Reporting & Continuous Improvement: Provide status updates, generate reports, and share insights on operational trends. Participate in after‑action reviews to help improve future processes.
  • Cross‑Functional Collaboration: Work closely with IT, Clinical Systems teams, and external vendors involved in hosting or supporting clinical data applications.

Required Skills & Qualifications

  • Educational Background: A Bachelor’s degree in Pharmacy, Life Sciences, or a related discipline.
  • Attention to Detail & Organization: Strong focus on accuracy, with good organizational skills and the ability to manage multiple tasks while prioritizing effectively.
  • Communication & Teamwork: Excellent verbal and written communication skills, along with strong interpersonal abilities to work collaboratively within cross‑functional teams.
  • Technical Skills: Proficiency in Microsoft Office applications, combined with good analytical thinking and problem‑solving capability.

Why Join GSK?

  • Work for a Global Biopharma Leader
    Join a world‑renowned organization shaping the future of healthcare through innovation, digital transformation, and next‑generation clinical technologies.
  • Cutting‑Edge Data & Digital Environment
    As part of the DS&M team, you’ll work with advanced EDC systems, ePRO platforms, automation tools, and data validation technologies, gaining hands‑on experience with industry‑leading systems.
  • Strong Learning & Career Development
    GSK offers structured training through Learning Hub, continuous upskilling, and mentorship—helping you grow into roles in clinical data management, digital operations, analytics, and regulatory data sciences.
  • Global Project Exposure
    Work on international clinical trials and collaborate with IT, Clinical Systems, Vendors, and cross‑functional global teams, giving you real-world exposure to global R&D processes.
  • Innovation‑Driven Culture
    GSK encourages innovation, problem‑solving, and process improvement, enabling you to contribute meaningfully to digital health evolution and smarter clinical development.
  • Purpose‑Driven Work
    Every task you perform directly supports GSK’s mission to get ahead of disease together, delivering better health outcomes for millions of patients worldwide.

How to Apply

Interested candidates should apply only through the official company career website using the link provided below.

Apply Here

Important Disclaimer

This job post is shared for informational purposes only, based on publicly available job details. Candidates are advised to verify eligibility, job responsibilities, and application procedures from the official IQVIA website before applying.

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FAQ – Clinical Data System Analyst

1. Is this role suitable for freshers?

This role is best suited for candidates with some exposure to clinical research, clinical data management, pharmacovigilance, analytics, or digital health systems. However, GSK provides structured training for the right entry-level candidate.

2. What educational background is required?

Candidates typically come from:

  • Life Sciences
  • Pharmacy
  • Biotechnology
  • Data science/analytics or related technical fields

3. Will I work with EDC systems?

Yes. A key responsibility is working with Electronic Data Capture (eDC) and ePRO systems, including system development, testing, and configuration.

4. Will I interact with cross‑functional teams?

Yes. You will collaborate with IT teams, Clinical Systems groups, vendors, and global study teams.

5. What compliance responsibilities are included?

You must follow SOPs, regulatory guidelines, quality plans, and maintain accurate documentation within eTMF.

6. Does the role involve reporting or metrics?

Yes. Analysts provide status updates, operational reports, and contribute to continuous improvement discussions.

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