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Clinical Data Reviewer

Tcs
TCS
2-4 years
preferred by company
10 Jan. 13, 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

Job Title: Clinical Data Reviewer – Mumbai, India
Location: Mumbai, Maharashtra | Full-Time
Experience Required: 2–4 years in Clinical Data Management or related roles

About the Role
We are seeking a meticulous Clinical Data Reviewer to join our Mumbai team. This role is ideal for candidates with 2–4 years of experience in clinical data management or clinical research, who are eager to contribute to high-quality study deliverables and ensure data integrity across clinical trials. The position involves working closely with Clinical Data Managers, study teams, and external stakeholders to monitor, review, and validate clinical data, ensuring compliance with study protocols and regulatory standards.

Key Responsibilities

  • Prepare and review eCRF specifications, Edit Check Specifications, and other study-specific setup documents.

  • Review and finalize Protocol Deviation Documents and study protocol deviations.

  • Develop and approve eCRF completion guidelines and study specifications.

  • Create and review Test Scripts for Edit Checks and UAT (User Acceptance Testing) scripts.

  • Coordinate with study teams to manage timelines, resolve issues, and ensure adherence to project plans.

  • Monitor and review study deliverables, ensuring quality, completeness, and compliance.

  • Maintain DMP metrics and participate in weekly project status meetings.

  • Identify and communicate issues related to validation procedures, site data flow, or discrepancies with Operations Managers, Clinical Data Managers, monitors, and clients.

  • Support the execution of data listing programs and dataset reviews for patient data consistency, quality, and completeness.

  • Utilize data management tools to monitor data quality, completeness, and timeliness for assigned study sites.

  • Identify areas for process improvement and assist in implementing aligned enhancements.

  • Provide hands-on support in data management tasks alongside Clinical Data Managers as needed.

Qualifications & Skills

  • Bachelor’s or Master’s degree in Pharmacy, Life Sciences, or related field (B.Sc, M.Sc, B.Pharm).

  • 2–4 years of experience in clinical data management, clinical trials, or related areas.

  • Strong knowledge of eCRF, Edit Checks, UAT, DMP metrics, and clinical trial protocols.

  • Proficient in data management tools and software used for clinical data review.

  • Excellent attention to detail, organizational, and communication skills.

  • Ability to work independently, manage multiple tasks, and collaborate effectively with cross-functional teams.

Why Join Us

  • Work in a dynamic clinical research environment contributing to global trials.

  • Opportunities for career growth, skill enhancement, and professional development.

  • Collaborate with experienced teams across Clinical Data Management, Operations, and external stakeholders.

  • Gain exposure to end-to-end clinical trial data lifecycle and advanced data management practices.

Apply Now
Join our Mumbai team as a Clinical Data Reviewer and play a key role in ensuring accuracy, quality, and compliance in clinical trials. Submit your CV online to be considered for this exciting opportunity.


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