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Clinical Data Team Lead - Veeva

Thermo Fisher Scientific
Thermo Fisher Scientific
4-6+ years
Not Disclosed
Bangalore, Remote
10 Feb. 14, 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

Lead, Clinical Data Team Lead 

Location: Remote (India)
Job Type: Full-Time
Experience Level: Mid to Senior – 4 to 6+ years clinical data management experience required
Category: Clinical Research / Clinical Data Management
Job ID: R-01341189

Role Overview
Thermo Fisher Scientific, a global leader in scientific services and clinical research solutions, is seeking an experienced Lead, Clinical Data Team Lead (CDTL) to manage and lead end-to-end clinical data management activities in support of global clinical trials. This fully remote position based in India offers responsibility for overseeing data quality, regulatory compliance, and workflow deliverables from study setup through database lock.

As a CDTL, you will serve as the primary data management lead for assigned studies, ensuring high-quality deliverables, stakeholder alignment, and operational excellence while mentoring junior staff and liaising with cross-functional teams.

Key Responsibilities

  • Lead and manage all clinical data management activities for assigned studies, ensuring compliance with protocols, SOPs, and global regulatory standards including ICH-GCP.

  • Serve as the primary liaison with project leads, clients, and internal stakeholders on all data management deliverables.

  • Oversee development, maintenance, and quality review of CDM documentation and study-specific deliverables.

  • Monitor study metrics, timelines, and risks; prepare and present regular status reports.

  • Provide mentorship and training to clinical data management staff, strengthening team capabilities.

  • Support project planning, resource forecasting, out-of-scope identification, and bid defense activities where required.

  • Maintain strict data integrity, confidentiality, and inspection readiness across all assigned studies.

Experience & Qualifications

  • Bachelor’s degree or equivalent in Life Sciences, Pharmacy, Biotechnology, Clinical Research, or related discipline.

  • 4 to 6+ years of hands-on experience in clinical data management within a CRO, pharmaceutical, or biotech environment, with leadership responsibility.

  • Demonstrated experience with Veeva EDC and/or RAVE EDC platforms is required.

  • Proven ability to lead clinical data management activities, mentor teams, and manage multiple deliverables in a remote, global setting.

  • Strong understanding of clinical trial processes, regulatory requirements, and data quality standards.

  • Excellent English communication skills, both written and verbal, with strong analytical and problem-solving capabilities.

Why Join Thermo Fisher Scientific
Thermo Fisher Scientific is a globally recognized leader in serving science, supporting clinical research and pharmaceutical development across more than 100 countries. In this role, you will:

  • Lead clinical data management for international clinical trials across multiple phases and therapeutic areas.

  • Collaborate with global project teams, sponsors, and cross-functional partners.

  • Work within a mature Functional Service Provider (FSP) delivery model that supports professional growth, structured learning, and career development.

  • Contribute to data quality excellence and delivery of life-changing therapies to patients worldwide.

How to Apply
Submit your application via thepharmadaily.com to join a global team advancing clinical research and data management excellence.