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Clinical Data Management

TCS
3-6 years
INR 7 LPA – 14 LPA
Mumbai, India
1 June 15, 2026
Job Description
Job Type: Full Time Education: M.Pharm/B.Pharm or M.Sc. Skills: Clinical SAS Programming, Clinical Trials, Detail-Oriented, Drug Development, Lifesciences, Negotiation Skills, Regulatory Compliance, Communication Skills, CPC Certified, Data Analysis, Document Management, Life Science, Regulatory Compliance, Waterfall Model, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing

Clinical Data Management Associate

Location: Mumbai, Pune, Bengaluru, India
Employment Type: Full-Time

Job Summary

The Clinical Data Management Associate is responsible for supporting clinical trial data management activities, ensuring the collection, review, reconciliation, validation, and maintenance of high-quality clinical data throughout the study lifecycle. The role involves collaboration with cross-functional study teams, management of clinical databases, query resolution, vendor reconciliation, and ensuring compliance with regulatory and quality standards.


Key Responsibilities

Clinical Data Review & Management

  • Review and understand study protocols, data management plans, and project timelines.

  • Perform ongoing clinical data review, validation, and quality checks throughout the study lifecycle.

  • Manage data discrepancies, queries, and reconciliation activities to ensure data accuracy and completeness.

  • Escalate significant data issues and discrepancies to appropriate stakeholders.

Query Management & Data Reconciliation

  • Conduct query generation, tracking, and resolution activities.

  • Perform SAE (Serious Adverse Event) reconciliation and vendor data reconciliation.

  • Execute external data reviews and manual discrepancy checks.

  • Ensure all queries are resolved within established timelines.

Database Development & Validation

  • Develop specifications for edit checks, listings, and Data Validation Specifications (DVS).

  • Support implementation and testing of edit checks within clinical databases.

  • Perform User Acceptance Testing (UAT) for study databases and system enhancements.

  • Verify database functionality and compliance with study requirements.

Study Setup & Documentation

  • Assist with study startup activities and database setup processes.

  • Develop and maintain study-specific procedures, documentation, and work instructions.

  • Maintain complete and audit-ready data management study files.

  • Ensure compliance with company SOPs, regulatory requirements, and industry standards.

Reporting & Metrics

  • Support the preparation of study status reports and data management metrics.

  • Ensure effective implementation of study tracking and reporting processes.

  • Provide study-related reports and updates to the Trial Data Manager (TDM) as requested.

  • Monitor study progress and identify potential risks impacting data quality or timelines.

Cross-Functional Collaboration

  • Participate in internal and sponsor-facing study team meetings.

  • Provide data management updates to cross-functional stakeholders.

  • Collaborate with clinical operations, biostatistics, pharmacovigilance, and vendor teams.

  • Identify out-of-scope activities and communicate concerns to project leadership.

Quality & Compliance

  • Ensure delivery of high-quality, error-free clinical data.

  • Support audit readiness and regulatory inspection activities.

  • Adhere to GCP, ICH guidelines, SOPs, and applicable regulatory requirements.

  • Contribute to continuous process improvement initiatives within clinical data management.


Required Qualifications

Education

  • Bachelor's or Master's degree in Pharmacy, Life Sciences, Clinical Research, Biotechnology, Nursing, or a related scientific discipline.

Experience

  • 3–6 years of experience in Clinical Data Management, Clinical Research, or Clinical Operations.

  • Experience working in pharmaceutical, biotechnology, CRO, or healthcare research environments.

  • Hands-on experience with clinical databases, query management, and data reconciliation.