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Clin Data Team Lead

Thermo Fisher Scientific
Thermo Fisher Scientific
4-5.5 years
preferred by company
10 Jan. 26, 2026
Job Description
Job Type: Full Time Remote 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

Clinical Data Team Lead (CDTL)

Location: India (Remote)
Job Type: Full-Time
Work Mode: Fully Remote
Category: Clinical Research | Clinical Data Management
Job ID: R-01338262


Job Overview

A leading global Contract Research Organization (CRO) is seeking an experienced Clinical Data Team Lead (CDTL) to support international clinical research programs. This role offers end-to-end ownership of data management activities across one or more clinical studies, from study setup through database lock.

The Clinical Data Team Lead will act as the primary data management lead, ensuring high-quality, inspection-ready datasets while maintaining strict compliance with global regulatory standards, SOPs, and study protocols. This position is fully remote and aligned to a global Functional Service Provider (FSP) model supporting a major biopharmaceutical sponsor.


Key Responsibilities

  • Serve as the lead Clinical Data Manager for assigned studies, overseeing end-to-end data management activities

  • Apply protocol requirements to data management workflows and guide study teams on daily execution

  • Act as the primary liaison with Project Leads, sponsors, and internal stakeholders for all data management deliverables

  • Develop, maintain, and review study-specific data management documentation in line with CDM standards

  • Conduct independent quality reviews of data management outputs and ensure inspection readiness

  • Develop and deliver study-specific training to Clinical Data Management team members

  • Produce and present regular study status reports, including metrics, risks, and mitigation plans

  • Monitor timelines, quality indicators, and study performance metrics

  • Support project forecasting, resource planning, and identification of out-of-scope activities

  • Assist with contract modification processes and financial tracking where applicable

  • Mentor, train, and guide junior data management staff

  • Support bid defense meetings and proposal development as required

  • Independently perform assigned data management activities with a strong focus on quality and efficiency


Education and Experience Requirements

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

  • Minimum 4 to 5.5 years of experience in Clinical Data Management within a CRO, pharmaceutical, or biotech environment

  • Prior experience in a Lead Data Management role is preferred

  • Hands-on experience with RAVE and/or Veeva EDC systems is mandatory


Required Skills and Competencies

  • Strong understanding of clinical trial processes, protocols, and regulatory requirements (ICH-GCP)

  • Proven ability to lead and mentor clinical data management teams

  • Excellent written and verbal communication skills with strong English proficiency

  • Strong organizational, analytical, and problem-solving abilities

  • High attention to detail and commitment to data quality

  • Ability to work independently with minimal supervision in a remote environment

  • Strong stakeholder management and client-facing skills

  • Ability to manage timelines, identify risks, and adapt to changing project demands

  • High level of confidentiality when handling clinical and proprietary data


Career Growth and Development

This role supports a globally recognized biopharmaceutical sponsor known for innovation in specialty medicines, vaccines, and scientific research. As part of a mature FSP delivery model, you will collaborate with global data science and clinical operations teams on high-visibility clinical programs.

The FSP model emphasizes continuous learning through structured training, mentorship, and stretch assignments. Career progression opportunities include advancement to Senior Clinical Data Manager, CDM Project Manager, or Data Standards and Programming roles, based on performance and business needs.


Why Join This Opportunity

  • Fully remote clinical data leadership role based in India

  • Exposure to global, multi-phase clinical trials across therapeutic areas

  • End-to-end study ownership from setup through close-out

  • Opportunity to work with advanced EDC platforms and AI-enabled data workflows

  • Strong focus on quality, partnership, and long-term career development

  • Competitive environment supporting professional growth in global clinical research


About Thermo Fisher Scientific

Thermo Fisher Scientific Inc. is a global leader in scientific services, with annual revenue exceeding USD 44 billion. The organization supports customers across life sciences research, clinical development, diagnostics, and laboratory operations through industry-leading brands such as Thermo Scientific, Applied Biosystems, Invitrogen, Patheon, and PPD.

Thermo Fisher Scientific is an equal opportunity employer and is committed to fostering a diverse and inclusive workforce.


Apply now through thepharmadaily.com to advance your career as a Clinical Data Team Lead in a global, innovation-driven clinical research environment.a