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Clinical Data Reviewer

Tcs
TCS
2-4 years
preferred by company
10 Jan. 19, 2026
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

Clinical Data Reviewer

Experience Required: 2–4 Years
Location: Mumbai, India
Employment Type: Full-time
Function: Business Process Services | Clinical Research
Role Level: Executive
Job ID: 389826
Apply By: 07 April 2026


Job Overview

We are seeking a detail-oriented Clinical Data Reviewer to support clinical data management activities for global clinical studies. This role is ideal for professionals with hands-on experience in eCRF review, edit checks, UAT activities, and data quality oversight within a clinical research or CRO environment.

The Clinical Data Reviewer will work closely with Clinical Data Managers, study teams, sites, and clients to ensure high-quality, compliant, and timely clinical data delivery.


Key Responsibilities

Clinical Data Review & Study Setup

  • Prepare and review eCRF specifications, edit check specifications, and study-specific setup documentation

  • Review and finalize eCRF completion guidelines and study specifications

  • Perform eCRF review and approval activities in alignment with protocol requirements

Protocol & Deviation Management

  • Review protocol deviation documentation and assess study protocol deviations

  • Identify data inconsistencies and validation issues during study conduct

UAT & Validation Activities

  • Create and review test scripts for edit checks and User Acceptance Testing (UAT)

  • Review UAT plans, execution results, and UAT reports prepared by Clinical Data Managers

  • Complete deployment checklists to support study go-live

Data Quality & Reporting

  • Ensure quality, consistency, and completeness of study deliverables

  • Support data listings execution and dataset reviews for patient-level data validation

  • Maintain and review Data Management Plan (DMP) metrics

  • Participate in weekly status meetings and ongoing study tracking

Stakeholder Communication & Process Improvement

  • Communicate site-level data issues including discrepancies, data flow challenges, and quality concerns with sites, CRAs, internal teams, and clients

  • Coordinate with cross-functional study teams to manage timelines and resolve issues

  • Identify and drive process improvement initiatives aligned with project objectives

Operational Support

  • Utilize clinical data management tools to monitor data quality and timeliness

  • Provide hands-on production support alongside Clinical Data Managers as required


Required Qualifications

  • Bachelor’s degree in Pharmacy, Life Sciences, or a related discipline

  • Master’s degree (MSc or equivalent) preferred


Required Experience

  • 2 to 4 years of experience in clinical data management or clinical research

  • Proven experience with eCRF review, edit checks, UAT, and clinical data validation

  • Prior exposure to global clinical trials and regulatory-driven environments is preferred


Key Skills & Competencies

  • Clinical Data Management and Data Review

  • eCRF design and validation

  • Protocol deviation and discrepancy management

  • Strong analytical and problem-solving skills

  • Excellent communication and coordination abilities

  • Proficiency with clinical data management systems and tools


Why Apply Through The Pharma Daily

This role is well-suited for professionals seeking Clinical Data Reviewer jobs in Mumbai, clinical data management careers, and global clinical research opportunities. The listing is optimized for global visibility across search engines and AI-powered job platforms.