GSK Hiring for Clinical Compliance Associate: Apply Now

ByPharma Hiring Hub

Global biopharma innovator GSK is recruiting for the role of Clinical Compliance & Improvement Associate within its Development Operations division. The position is based in Bangalore, India, with additional opportunities available in Warsaw (Poland) and Stevenage (UK).

This role is ideal for professionals with 1 to 5 years of experience in areas such as clinical operations, GCP compliance, audit or inspection readiness, quality management systems, or clinical trial process improvement. It offers an excellent platform to strengthen your expertise in clinical compliance oversight, inspection preparedness, and continuous improvement initiatives across global clinical studies.

Joining GSK in this capacity provides exposure to international teams, cross‑functional collaboration, and a chance to contribute to high‑quality, globally compliant clinical trial delivery.

GSK hiring for clinical data associate

Job Overview

  • Position: Clinical Compliance Associate
  • Department: CDM
  • Location: Bangalore (Hybrid – 2–3 days/week office)
  • Experience: 1 to 5 Years
  • Qualification: B.Pharm, M.Pharm, Pharm.D, Msc, BSc, Lifesciences, Nursing , Clinical Research
  • Job Type: Full-Time
  • Application Deadline: 6 March 2026

Key Responsibilities

  • Support ongoing compliance monitoring activities to identify operational trends, potential risks, and emerging signals within assigned clinical teams.
  • Assist in the execution of compliance checks, routine monitoring, and follow‑up reviews to ensure that corrective and preventive actions are fully effective.
  • Collect, analyze, and interpret compliance‑related data, turning findings into meaningful insights that guide improvement plans and operational priorities.
  • Present compliance dashboards, summaries, or reports to key stakeholders as part of routine governance.
  • Participate in issue management activities, including logging new issues, tracking progress, escalating concerns when required, and supporting communication of actions and resolutions.
  • Assist in maintaining a state of continuous inspection and audit readiness by preparing essential documentation, compiling evidence packages, and supporting responses during regulatory or quality inspections.
  • Contribute to process improvement initiatives by supporting data collection, performing basic root‑cause analysis, facilitating small improvement projects, and coordinating with cross‑functional teams as needed.

Required Skills & Qualifications

  • A degree in Life Sciences, Pharmacy, Nursing, Clinical Research, or a closely related field. Candidates with equivalent relevant experience will also be considered.
  • 1–5 years of experience in clinical operations, quality assurance, compliance, clinical trial support, or other related functions within the life sciences or healthcare sector.
  • Solid understanding of Good Clinical Practice (GCP) guidelines and a working knowledge of end‑to‑end clinical trial conduct.
  • Hands‑on experience in evaluating operational or compliance data to identify trends, signals, gaps, or process improvement opportunities.
  • Strong spoken and written communication skills in English, with the ability to work effectively with global teams.
  • Willingness and ability to work in a hybrid setup, with regular attendance required at the local R&D office.

Preferred Skills & Experience (Good to Have)

  • Prior involvement in regulatory inspections or internal audits, supporting documentation, evidence gathering, or compliance activities.
  • Familiarity with clinical quality systems, issue management tools, deviation tracking, or general study oversight processes.
  • Experience conducting root cause analysis and helping implement Corrective and Preventive Actions (CAPA) to resolve issues effectively.
  • Ability to work comfortably across multiple teams, stakeholders, and functions within a matrix‑driven environment.
  • Proficiency in tools such as Microsoft Excel, Power BI, basic AI/automation tools, or other data visualization platforms—along with strong reporting and presentation skills.
  • Clinical Systems Familiarity:
    Exposure to clinical platforms such as Veeva, or other documentation and trial management systems.
  • Industry Background:
    Previous experience in a pharmaceutical company, biotech, or contract research organization (CRO) is a strong plus.

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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