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Clin Data Team Lead

Thermo Fisher Scientific
Thermo Fisher Scientific
4-6 years
preferred by company
10 Jan. 20, 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

Job Title: Clinical Data Team Lead (CDTL)
Location: Remote, India
Job Type: Full-Time
Experience Required: 4–6 Years
Job ID: R-01338262


About the Company

Join Thermo Fisher Scientific, a global leader in serving science with a mission to make the world healthier, cleaner, and safer. Our Clinical Research Services team delivers innovative drug development solutions to the world’s leading pharmaceutical and biotech companies. With operations across 100+ countries and support for thousands of clinical trials, our team combines scientific expertise, technology, and global collaboration to accelerate the development of life-changing therapies.

As part of our FSP Data Management team, you will support a globally recognized biopharmaceutical client and work within a mature delivery model emphasizing quality, compliance, and innovation.


Role Overview

The Clinical Data Team Lead (CDTL) is responsible for leading end-to-end clinical data management for one or more studies, from study setup through database lock. This role involves directing CDM activities, ensuring adherence to protocol and regulatory requirements, maintaining high-quality deliverables, and liaising with clients and project leadership.

You will mentor and train team members, oversee project metrics, produce status reports, support resource forecasting, identify out-of-scope work, and contribute to business development and bid activities as needed. This role offers significant exposure to modern CDM practices, including RAVE and Veeva EDC, AI-enabled workflows, and global clinical trial operations.


Key Responsibilities

  • Lead and oversee data management activities across assigned studies, ensuring compliance with GCP, SOPs, and client expectations

  • Apply protocol requirements to team workflows and provide guidance to project staff

  • Serve as the primary liaison to project leads, clients, and internal stakeholders

  • Maintain and review study-specific CDM documentation, ensuring accuracy and completeness

  • Train and mentor junior staff, providing guidance on data review, query resolution, and CRF implementation

  • Generate project-specific status reports and monitor study metrics

  • Support resource forecasting, identify potential out-of-scope activities, and assist with contract modifications

  • Contribute to bid preparation and defense meetings when required

  • Manage administrative and financial aspects of assigned projects, ensuring efficient and high-quality delivery

  • Ensure data integrity and inspection readiness across all assigned studies


Education & Experience Requirements

  • Bachelor’s degree or equivalent in Life Sciences, Pharmacy, or related field

  • 4–6 years of experience in clinical data management, with proven expertise in RAVE or Veeva EDC

  • Strong knowledge of clinical trial processes, medical/clinical terminology, and regulatory requirements


Skills & Competencies

  • Strong leadership and team management skills; ability to mentor and guide CDM staff

  • Excellent written and verbal communication in English

  • Strong analytical, organizational, and problem-solving abilities

  • Ability to maintain confidentiality with clinical data and client information

  • Demonstrated flexibility, adaptability, and initiative in a dynamic environment

  • Proficient in interactive computer programs and CDM software

  • Ability to manage multiple projects and meet deadlines in a fast-paced global setting

  • Knowledge of project metrics, status reporting, and study forecasting


Career Growth

This role offers long-term career opportunities within Clinical Data Management (e.g., Senior CDM, CDTL, CDM Project Manager) or potential transition into Data Standards, Programming, or other global clinical data roles. The FSP delivery model supports continuous learning, mentorship, and stretch assignments to expand technical and leadership expertise.


Why Join Thermo Fisher Scientific

  • Global exposure: Work on international clinical trials across phases and therapeutic areas

  • End-to-end ownership: Manage clinical data delivery from study setup to database lock

  • Hands-on experience: Gain expertise in modern CDM, EDC, and AI-enabled clinical workflows

  • Professional growth: Strengthen project management, risk management, financial tracking, and analytical skills

  • Impactful work: Contribute to life-changing medicines that improve patient outcomes worldwide


About Thermo Fisher Scientific
Thermo Fisher Scientific Inc. is a global leader in science, with more than 90,000 employees delivering innovative technologies and pharmaceutical services through brands like Thermo Scientific, Applied Biosystems, Invitrogen, Fisher Scientific, Unity Lab Services, and Patheon. Our mission is to enable our customers to make the world healthier, cleaner, and safer. For more information, visit www.thermofisher.com.

Equal Employment Opportunity Statement:
Thermo Fisher Scientific is an Equal Opportunity Employer. All qualified applicants will receive consideration without regard to race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, gender identity, or other legally protected status.


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