Manager, Clinical Data Management (CDM) – Bengaluru, India (Hybrid)
Salary / Compensation: Not disclosed in the job description.
Job Summary
IQVIA is seeking a Manager, Clinical Data Management (CDM) to own end‑to‑end data management delivery across single and multi‑service clinical studies. You will act as Data Team Lead (DTL)—planning, executing and closing projects while ensuring high‑quality, audit‑ready databases are delivered on time, within budget, and to ICH‑GCP / GCDMP standards. Perfect for a CDM professional with 3–4+ years’ experience (≥1 year as CDM project lead) who’s ready to lead teams, drive process excellence, and partner closely with sponsors and cross‑functional stakeholders.
Key Responsibilities
Lead study start‑up, conduct & close‑out activities; gather setup requirements and translate them into robust CDM plans.
Own data cleaning strategy and delivery to ensure high‑quality, inspection‑ready datasets.
Perform/oversee validation of new device integrations and database revisions.
Drive project tracking, risk identification, mitigation and corrective actions.
Ensure all CDM deliverables meet contract/SOW timelines, KPIs & quality metrics.
Support, train and mentor new joiners and junior CDM staff.
Lead internal study meetings, sponsor meetings, audits & kick‑offs.
Collaborate with programming/automation teams to innovate and optimize CDM processes.
Contribute to and review SOPs, WIs, DMPs and other core process documents.
Maintain full compliance with eSOPs, trainings, ICH‑GCP, GCDMP and regulatory expectations.
Required Skills & Qualifications
Bachelor’s degree in health/clinical/biological/mathematical sciences (or related).
3–4 years of Clinical Data Management experience with ≥1 year as CDM project lead/DTL.
Advanced understanding of the drug development life cycle, ICH‑GCP, GCDMP.
Strong command of EDC platforms, data review, query management, data reconciliation (3rd‑party labs/eCOA), and database lock processes.
Excellent stakeholder management, project management, risk management, budgeting & timeline control.
Proficient with Microsoft Excel, Word, Outlook; familiarity with CDISC standards (SDTM/ADaM) is a plus.
Excellent written & verbal English communication skills.
(Common pharma/CDM keywords to boost SEO & discoverability: Clinical Data Management, EDC, CDISC, SDTM, ADaM, eCOA, MedDRA, ICH‑GCP, GCDMP, DMP, DTL, database lock, query management, risk-based data review.)
Perks & Benefits
Hybrid work model for flexibility and work–life balance.
Work with a global leader in clinical research and healthcare analytics.
Career development, training & mentorship opportunities.
Exposure to large, global, multi‑service clinical programs and cutting‑edge data technologies.
Company Description
IQVIA is a global leader in clinical research services, commercial insights, and healthcare intelligence, helping life sciences companies accelerate the development and commercialization of innovative therapies. With advanced analytics, technology, and domain expertise, IQVIA improves patient outcomes and population health worldwide.
Work Mode: Hybrid – Bengaluru, India
Apply Now
Lead high‑impact CDM programs with one of the world’s most respected clinical research organizations. Apply now to become IQVIA’s next Manager, Clinical Data Management.
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