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Senior Clinical Data Manager I

4-7 years
Not Disclosed
10 July 24, 2025
Job Description
Job Type: Full Time Hybrid 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

 

Senior Clinical Data Manager I – AstraZeneca (Bangalore, India)

Application deadline: 27 July 2025 (3 days left to apply)
Date posted: 22 July 2025
Job ID: R-231774
Work type: Full-time
Work mode: Not specified (assume On-site/Hybrid – Bangalore)
Compensation / Salary: Not disclosed in the job description


Job Summary

AstraZeneca is seeking a Senior Clinical Data Manager I to lead, plan, and deliver end‑to‑end Clinical Data Management (CDM) activities across study start-up, conduct, and closeout. You will coordinate with Data Management Vendors, clinical teams, statisticians, and cross‑functional partners to ensure GCDMP- and regulatory-compliant data integrity. If you bring strong experience in EDC systems, query management, third-party data reconciliation, CDISC standards, and audit/inspection readiness, this role lets you make a measurable impact on global studies.


Key Responsibilities

  • Lead study-level CDM operations across start-up, conduct, and closeout (UAT, query management, data cleaning, reconciliation).

  • Coordinate CDM deliverables with Data Management Vendors; track timelines, risks, and quality.

  • Maintain clinical database integrity, ensuring business continuity of CDM processes and standards.

  • Provide study status updates to clinical teams and support data quality oversight.

  • Contribute to regulatory inspections/audits and documentation readiness.

  • Understand therapeutic area‑specific data capture standards and implement them consistently.

  • Mentor junior team members and support ad‑hoc CDM requests.

  • Identify risks proactively and partner with Study Data Managers to implement mitigation plans.


Required Skills & Qualifications

  • Graduate degree in Life Sciences / Pharmacy / Nursing or related discipline.

  • End‑to‑end Clinical Data Management experience in Biotech/Pharma/CRO.

  • Working knowledge of GCDMP, regulatory requirements, and EDC platforms.

  • Proven experience in query management, data reconciliation, CRF/database development, and data cleaning.

  • Strong communication, analytical, organizational, and time-management skills.

  • Ability to work flexibly on multiple simultaneous projects within global teams.

Desirable Skills

  • Understanding of drug development processes and clinical data system interoperability.

  • Knowledge of database structures, programming languages (SQL, 4GL, VBA, R), and CDISC data standards.

  • Experience working effectively with external partners/vendors.


Perks & Benefits (as typical of AstraZeneca; not explicitly listed)

  • Work with a data- and technology-driven global biopharma leader.

  • Learning, mentorship, and career growth in a high-impact CDM function.

  • Inclusive culture focused on innovation, curiosity, and patient impact.

  • Opportunity to contribute to global audits/inspections and high-profile studies.


Company Description

AstraZeneca is a science-led global biopharmaceutical company committed to transforming patient outcomes through innovation. By combining data, technology, and deep scientific expertise, AstraZeneca addresses complex diseases and advances access to care worldwide within an inclusive, diverse culture.


Work Mode

On-site / Hybrid (not explicitly specified) – Bangalore, India


Call-to-Action

Ready to lead global Clinical Data Management deliverables and ensure inspection-ready data quality? Apply now for the Senior Clinical Data Manager I role at AstraZeneca before 27 July 2025.