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Clin Data Team Lead

Thermo Fisher Scientific
Thermo Fisher Scientific
4-6 years
preferred by company
10 Jan. 7, 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: Remote, India
Employment Type: Full-Time
Work Mode: Fully Remote
Job ID: R-01338262
Category: Clinical Research | Clinical Data Management
Experience Required: 4–6 Years


Job Overview

Thermo Fisher Scientific, through its PPD® Clinical Research Services, is seeking an experienced Clinical Data Team Lead (CDTL) to join its global Functional Service Provider (FSP) data management team in India. This fully remote role offers the opportunity to lead end-to-end clinical data management activities for global clinical trials across multiple therapeutic areas.

As a CDTL, you will serve as the lead data manager for assigned studies, overseeing data management activities from study setup through database lock, ensuring quality, compliance, timelines, and stakeholder alignment.


Key Responsibilities

  • Act as the primary Clinical Data Management (CDM) lead for one or more clinical studies.

  • Apply protocol requirements to daily data management activities and guide team members accordingly.

  • Direct and oversee all CDM deliverables, ensuring compliance with ICH-GCP, SOPs, and regulatory standards.

  • Develop, maintain, and review data management documentation in line with established CDM guidelines.

  • Serve as a key liaison with Project Leads, clients, and internal stakeholders for all data management matters.

  • Monitor study progress using metrics and dashboards; prepare and deliver regular status reports.

  • Conduct study-specific training sessions and mentor junior CDM team members.

  • Support resource forecasting, effort estimation, and identification of out-of-scope activities.

  • Assist with contract modifications, administrative oversight, and financial tracking of assigned studies.

  • Participate in business development activities, including bid preparation and bid defense meetings, as required.

  • Ensure all data management tasks are completed independently with a strong focus on data quality and audit readiness.


Education & Experience Requirements

  • Education:

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

  • Experience:

    • Minimum 4 to 6 years of hands-on experience in Clinical Data Management

    • Prior experience as a Lead Data Manager or Senior Clinical Data Associate

    • Mandatory experience with RAVE EDC and/or Veeva EDC platforms


Required Skills & Competencies

  • Strong understanding of clinical trial data management processes across study phases

  • Ability to apply regulatory guidelines, SOPs, and client requirements in a structured manner

  • Excellent written and verbal communication skills with strong English proficiency

  • Strong analytical, organizational, and problem-solving abilities

  • Proven ability to work independently with minimal supervision

  • High level of integrity and confidentiality when handling clinical and proprietary data

  • Strong stakeholder management and customer-focused mindset

  • Demonstrated leadership skills, including training and mentoring study teams

  • Flexibility and adaptability in a dynamic global clinical research environment

  • Ability to manage timelines, assess risks, and respond proactively to project changes


Career Growth & Development

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

Career progression opportunities include:

  • Senior Clinical Data Manager

  • Clinical Data Team Lead (Senior CDTL)

  • Clinical Data Management Project Manager

  • Data Standards or Clinical Programming roles

Continuous learning is supported through structured learning pathways, mentorship, and stretch assignments.


Why Join Thermo Fisher Scientific

  • Fully remote role with global clinical trial exposure

  • End-to-end ownership of clinical data management activities

  • Opportunity to work on international, multi-phase clinical studies

  • Exposure to modern CDM technologies, including AI-enabled workflows

  • Strong emphasis on quality, partnership, and professional growth


About Thermo Fisher Scientific

Thermo Fisher Scientific is a global leader in serving science, with annual revenue exceeding USD 44 billion. With over 90,000 colleagues worldwide, the company supports life sciences research, clinical development, diagnostics, and pharmaceutical manufacturing. Its mission is to make the world healthier, cleaner, and safer through innovation and scientific excellence.

Thermo Fisher Scientific is an Equal Opportunity Employer and is committed to diversity, equity, and inclusion across its global workforce.


Apply Now

If you are an experienced Clinical Data Management professional seeking a fully remote leadership role with global exposure and long-term growth potential, this opportunity is ideal for you.