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Senior Analyst Clinical Data -New Delhi

0-2 years
Not Disclosed
10 Nov. 11, 2025
Job Description
Job Type: Full Time Education: B.Sc/M.Sc/M.Pharma/B.Pharma/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

Senior Analyst – Clinical Data

Location: New Delhi, India
Category: Medical and Clinical Affairs


Role Summary

Acts as the clinical database and data management subject matter expert on Clinical Project Teams. Responsible for ensuring data integrity, regulatory compliance, and effective implementation of data management standards across clinical trials.


Key Responsibilities

1. Clinical Project Team Collaboration

  • Attend Clinical Project Team meetings to gather business requirements and translate them into technical specifications.

  • Collaborate with shared service functions (Safety, Core Lab, etc.) to gather requirements and propose solutions.

  • Identify, analyze, and resolve complex data issues, exercising sound judgment and teamwork.

  • Train database end-users (internal and external) and maintain automated database training systems.

  • Capture and maintain database and system training records.

  • Assist in FDA and Quality audits involving clinical databases and data management.

  • Lead development and quality control (QC) of data management documents, including:

    • Data Management Plans (DMPs)

    • Data Review Guidelines

    • Database Validation Protocols

  • Ensure adherence to Standard Operating Procedures (SOPs) and data management best practices.


2. Clinical Database System Development

  • Collaborate with DM Management, Database Developers/Analysts, and Programmers to deliver database and system solutions.

  • Translate business requirements into technical specifications for:

    • eCRFs

    • Edit checks

    • Study notifications

    • Database customizations

  • Perform and document functional and user acceptance testing (UAT).

  • Implement data validation and quality control checks per study needs.

  • Communicate effectively with the Clinical Project Team and other stakeholders regarding timelines, deliverables, and workarounds.

  • Partner with Data Management team members to prioritize deliverables.

  • Maintain database account integrity and security.

  • Recommend process improvements for Clinical Data Management practices, SOPs, and work instructions.


3. Data Cleaning & Database Lock

  • Lead data review meetings with Clinical Project Team and Biostatistics to identify and resolve data cleaning issues.

  • Plan and monitor interim and final database locks; ensure all timelines are met.

  • Coordinate all aspects of data review, including:

    • Running validation procedures

    • Issuing queries

    • Database QC

    • SAE reconciliation

    • Medical coding

    • Database closure activities

  • Design tools and reports to document data review and support cleaning activities.

  • Lead and document data freeze activities with Clinical Project Team, Biostatistics, and SAS programmers.

  • Utilize SQL, database UI, and existing tools to identify and resolve data issues efficiently.


Core Competencies

  • Clinical Data Management Expertise

  • Regulatory Compliance Knowledge (FDA, Quality Audits)

  • Database Systems Knowledge (EDC, eCRF, Edit Checks)

  • Problem-Solving & Issue Resolution

  • Collaboration & Communication Skills

  • Process Improvement & SOP Adherence