Clin Data Team Lead

Thermo Fisher Scientific

4-5.6 years

preferred by company

India Remote

10 Feb. 2, 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) – Fully Remote (India)

Job ID: R-01338262
Job Type: Full Time
Category: Clinical Research / Clinical Data Management
Work Mode: Fully Remote
Location: India
Work Schedule: Monday to Friday (Standard Business Hours)

About the Role

We are seeking an experienced Clinical Data Team Lead (CDTL) to join a high-performing global Clinical Research Services team supporting large-scale, international clinical trials. This role offers end-to-end ownership of clinical data management activities, from study setup through database lock, within a mature Functional Service Provider (FSP) delivery model.

As a CDTL, you will serve as the lead data manager for one or more clinical studies, ensuring data quality, regulatory compliance, timeline adherence, and operational excellence. You will collaborate closely with project leadership, clients, and cross-functional teams while mentoring and guiding clinical data professionals.

Key Responsibilities

Lead and manage end-to-end clinical data management activities from study initiation to database lock.
Apply protocol requirements to data management workflows and guide team members in execution.
Act as the primary data management liaison with Project Leads, clients, and internal stakeholders.
Develop, maintain, and independently review data management documentation and deliverables in accordance with SOPs and CDM standards.
Deliver study-specific training to clinical data management staff and mentor junior team members.
Monitor study metrics, timelines, and risks; produce regular status reports for management and clients.
Support project planning activities including resource forecasting, effort estimation, and identification of out-of-scope work.
Assist with administrative and financial management of assigned studies.
Participate in business development activities such as bid preparation and bid defense meetings, as required.
Ensure strict adherence to regulatory guidelines, data integrity standards, and client expectations.

Education and Experience Requirements

Bachelor’s degree in Life Sciences, Pharmacy, Biotechnology, or a related discipline (or equivalent qualification).
Minimum 4 to 5.6 years of hands-on experience in Clinical Data Management within a CRO or pharmaceutical environment.
Proven experience leading studies as a Clinical Data Team Lead or Senior Clinical Data Manager.
Mandatory hands-on experience with RAVE and/or Veeva EDC platforms.
Experience working on global, multi-country clinical trials is strongly preferred.

Required Skills and Competencies

Strong understanding of clinical trial processes, CDM standards, and regulatory requirements.
Excellent written and verbal communication skills with strong attention to detail.
Demonstrated ability to manage timelines, prioritize tasks, and work independently with minimal supervision.
Strong analytical, organizational, and problem-solving abilities.
High level of integrity and confidentiality when handling clinical and proprietary data.
Proven leadership skills with the ability to train, guide, and motivate study teams.
Flexibility and adaptability in a fast-paced, global project environment.
Proficiency in clinical data systems and interactive computer applications.

Career Growth and Development

This role supports a globally recognized biopharmaceutical sponsor known for innovation across specialty medicines, vaccines, and advanced scientific research. As part of the FSP model, you will collaborate with global data science teams and contribute to high-visibility clinical programs.

The organization offers structured career development through:

Tailored learning pathways and mentorship
Exposure to complex, global clinical trials
Opportunities to progress into roles such as Senior CDM, Senior CDTL, CDM Project Manager, or transition into Data Standards or Clinical Programming, based on performance and business needs

Why Join Us

Work on international clinical trials across multiple phases and therapeutic areas.
Gain end-to-end ownership of clinical data delivery, from study setup to close-out.
Strengthen global project management, risk management, and analytical capabilities.
Build expertise in modern Clinical Data Management, including EDC platforms, data quality frameworks, and emerging AI-enabled workflows.
Be part of a mission-driven organization focused on bringing life-changing therapies to patients worldwide.

About Thermo Fisher Scientific

Thermo Fisher Scientific Inc. is a global leader in serving science, with annual revenue exceeding USD 44 billion. Our mission is to enable customers to make the world healthier, cleaner, and safer. With more than 90,000 colleagues worldwide, we deliver innovative technologies, pharmaceutical services, and laboratory solutions through industry-leading brands including Thermo Scientific, Applied Biosystems, Invitrogen, Fisher Scientific, Unity Lab Services, and Patheon.

Thermo Fisher Scientific is an Equal Employment Opportunity Employer.

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Clin Data Team Lead

Job Description

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