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Manager, Senior Central Testing Analyst

10+ years
₹35–45 LPA
99 Aug. 13, 2025
Job Description
Job Type: Full Time Education: B.Sc./M.Sc./B.Pharm/M.Pharm/Life science 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 Title: Manager, Senior Central Testing Analyst
Location: Chennai, India
Employment Type: Full-time

About the Company:
Pfizer is a global leader in biopharmaceutical innovation, committed to breakthroughs that change patients’ lives. Pfizer Research & Development serves as the driving force behind the company’s groundbreaking product pipeline, delivering life-changing medicines worldwide.

Role Overview:
As part of the Clinical Data Sciences (CDS) group within Clinical Development & Operations (CD&O), the Manager, Senior Central Testing Analyst is responsible for leading and delivering User Acceptance Testing (UAT) activities. The role ensures that deliverables meet quality standards and timelines for assigned studies, while also supporting development, system upgrades, automation validation, and high-quality technical processes for the Pfizer portfolio.

Key Responsibilities:

  • Oversee UAT activities, including CRF design testing, database build validation, and eData acquisition (Lab, ECG, PK/PD).

  • Allocate study assignments and manage workloads within a matrixed environment.

  • Create and track resource allocation and forecasting for the portfolio.

  • Conduct peer reviews, QC checks, and monitor operational metrics.

  • Perform risk assessment, RCA, and CAPA for quality issues.

  • Mentor UAT analysts and Data Managers, ensuring knowledge sharing and process improvement.

  • Standardize scripts for forms, edit checks, and reports.

  • Collaborate with Clinical Data Scientists and Study Data Managers to align timelines.

  • Ensure adherence to SOPs and regulatory standards (FDA, Health Canada).

  • Lead innovation initiatives and continuous process improvement in UAT.

  • Manage direct reports’ performance evaluations.

Qualifications & Skills:

  • Bachelor’s degree required; Health Sciences or Technology preferred.

  • 10+ years of clinical data management experience in pharma or CRO settings.

  • Strong background in test case writing and UAT execution.

  • Knowledge of CRF design, database build, edit checks, and data transfers.

  • Familiarity with clinical development regulatory requirements.

  • Understanding of Software Development Life Cycle (SDLC) and testing methodologies.

  • Proficiency in Microsoft Office tools.

  • Project and people management experience preferred.

Work Location Assignment: Hybrid

Estimated Salary: ₹35–45 LPA (Based on industry benchmarks for senior clinical data leadership roles in Chennai)