Clinical Data Team Lead (CDTL)
Location: Remote – India
Job ID: R-01338262
Employment Type: Full-time
Work Model: Fully Remote
Industry: Clinical Research | Contract Research Organization (CRO)
Functional Area: Clinical Data Management
About the Organization
Thermo Fisher Scientific, through its PPD® Clinical Research Services division, is a global leader in clinical research and development. Supporting the top 50 pharmaceutical companies and more than 750 biotechnology organizations, PPD® has delivered over 2,700 clinical trials across 100+ countries in the past five years. As part of Thermo Fisher Scientific, the organization plays a critical role in advancing innovative therapies that address complex global health challenges.
Job Overview
The Clinical Data Team Lead (CDTL) serves as the lead data manager for one or more clinical studies, providing end-to-end oversight of Clinical Data Management (CDM) activities from study start-up through database lock. This role ensures high-quality, compliant, and timely data delivery while acting as the primary data management contact for project leadership and sponsor teams. The position also includes team leadership, resource forecasting, and contribution to strategic and financial aspects of study execution within a Functional Service Provider (FSP) model.
Key Responsibilities
Clinical Data Management Leadership
Lead and oversee all CDM activities across assigned studies, ensuring adherence to protocol requirements, SOPs, and regulatory standards
Direct data management workflows from study setup, database development, and data cleaning through database lock
Project & Stakeholder Management
Serve as the primary liaison with Project Leads, sponsors, and internal stakeholders on all data management matters
Monitor study metrics, timelines, and risks; proactively escalate issues as needed
Produce and maintain project-specific status reports for management and sponsor review
Documentation, Quality & Compliance
Develop, maintain, and review data management documentation and deliverables in accordance with documented CDM guidelines
Ensure quality oversight through independent review of data management outputs
Team Leadership & Mentorship
Develop and deliver study-specific training for data management team members
Mentor and guide junior staff across all study-related CDM activities
Resource & Financial Support
Support project forecasting, effort estimation, and identification of resource requirements
Identify potential out-of-scope activities and support contract modification processes
Assist with administrative and financial management of assigned projects
Business Development Support
Participate in bid preparation and, where required, represent Data Management in bid defense meetings
Required Qualifications
Education
Bachelor’s degree or equivalent in life sciences, pharmacy, clinical research, or a related discipline
Experience
Minimum 4 to 5.6 years of professional experience in Clinical Data Management within a CRO or pharmaceutical organization
Demonstrated experience leading clinical data management activities for global clinical trials
Technical Skills
Hands-on experience with RAVE and/or Veeva EDC platforms
Strong understanding of the end-to-end clinical trial data lifecycle
Familiarity with regulatory requirements, SOPs, and global clinical research standards
Core Competencies
Excellent written and verbal communication skills in English
Strong organizational, analytical, and problem-solving abilities
Ability to work independently in a fully remote environment
Proven ability to train, mentor, and lead clinical data management teams
High level of data confidentiality and customer focus
Flexibility to adapt to changing project requirements and timelines
Career Growth & Development
This role supports a dedicated FSP client—a globally recognized biopharmaceutical organization with a strong track record in specialty medicines, vaccines, and scientific innovation. As part of a mature FSP delivery model, the CDTL will collaborate closely with global data science teams and contribute to high-visibility, complex clinical programs.
Thermo Fisher Scientific’s FSP model promotes continuous learning through structured career pathways, mentorship, and advanced training. Career progression opportunities include Senior Clinical Data Manager, Senior CDTL, Clinical Data Project Manager, or transitions into Data Standards and Programming roles.
Why Join Thermo Fisher Scientific
Work on international, multi-phase clinical trials across diverse therapeutic areas
Gain end-to-end ownership of clinical data delivery from setup to close-out
Build expertise in modern CDM, including EDC platforms and AI-enabled data workflows
Collaborate with global sponsors, CRO partners, and cross-functional teams
Be part of a science-driven organization committed to improving global health
Equal Opportunity Statement
Thermo Fisher Scientific is an equal opportunity employer. All qualified applicants will receive consideration without regard to race, color, religion, sex, age, nationality, disability, sexual orientation, gender identity, or any other status protected by applicable laws.
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