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Senior Analyst - Data Acquistion

0-2 years
Not Disclosed
10 Sept. 16, 2025
Job Description
Job Type: Full Time Education: B.Sc/ M.Sc/ M.Pharm/ B.Pharm/ Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Job Description

Site Name: Bengaluru Luxor North Tower
Posted Date: September 10, 2025


Role Overview

This role involves study set-up activities and the technical development of Electronic Data Capture (eDC) solutions and associated tools to support one or more clinical studies. The position requires technical oversight of data acquisition processes, vendor collaboration, and ensuring timely, high-quality delivery of study requirements in compliance with GxP and ICH standards.


Key Responsibilities

Study Set-up & Technical Development

  • Perform study set-up activities and develop eDC solutions and associated tools.

  • Assist in technical and vendor oversight of multiple data types for clinical studies.

  • Support delivery of clinical studies, depending on phase, complexity, and scope, with junior staff as required.

Study-Specific Responsibilities

  • Provide input to study design, clinical protocols, planning, and review of study documents.

  • Coordinate review, revision, and approval of study specification documents (e.g., operational requirements, specifications) and key vendor deliverables (including translations).

  • Identify, mediate, and resolve data acquisition issues.

  • Develop study eDC applications and related documents (e.g., forms, data validation checks, data extraction).

  • Ensure timely and quality delivery of all outputs.

  • Provide reports, updates, and risk assessments to the Study Data Manager.

  • Perform quality control checks on deliverables.

Process Improvement & Compliance

  • Contribute to process improvements, training, quality assessments, audits, and inspections.

  • Conduct after-action reviews to capture learnings and propose improvements.

  • Maintain extensive knowledge of GxP, ICH requirements, internal processes, and external regulations relevant to drug development.


Why Join GSK?

At GSK, we unite science, technology, and talent to get ahead of disease together. We aim to positively impact the health of 2.5 billion people by 2030, through innovation in specialty medicines and vaccines.

  • Therapeutic Focus Areas: Respiratory, Immunology & Inflammation, Oncology, HIV, and Infectious Diseases.

  • Our Culture: Ambitious for patients, accountable for impact, and guided by doing the right thing.

  • Commitment: Creating an environment where people thrive while making a real difference for patients worldwide.


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  • Any actions taken without authorization will be deemed unauthorized, and GSK will not be liable for associated fees.


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