Associate Clinical Data Team Lead (ACDTL)
Location: Remote – India
Job ID: R-01338261
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 business, is a global leader in advancing clinical research and accelerating the development of life-changing therapies. Over the past five years, the organization has supported the top 50 pharmaceutical companies and more than 750 biotechnology firms, delivering over 2,700 clinical trials across 100+ countries.
As part of Thermo Fisher Scientific, PPD® operates within one of the world’s most respected scientific organizations, dedicated to enabling customers to make the world healthier, cleaner, and safer.
Job Overview
The Associate Clinical Data Team Lead (ACDTL) serves as the assistant lead data manager on one or more clinical research projects. This role supports the Lead Data Manager across all phases of clinical data management, including study setup, data cleaning, database development, and close-out activities. The position is ideal for experienced Clinical Data Associates ready to step into a leadership and project coordination role within a global FSP (Functional Service Provider) model.
Key Responsibilities
Clinical Data Management & Study Support
Apply protocol requirements and data management standards to daily project activities
Support study setup, database build, edit check development, and user acceptance testing
Coordinate and oversee data cleaning activities to ensure data quality and timeline adherence
Team Leadership & Training
Deliver study-specific training to junior data management team members
Delegate data management tasks while maintaining quality and compliance standards
Project Coordination & Risk Management
Monitor study timelines, metrics, and risks; escalate issues proactively
Support the Lead Data Manager with risk management and project forecasting
Maintain and review clinical data management documentation in accordance with SOPs
Reporting & Stakeholder Interaction
Generate and maintain project-specific status reports for internal management, project managers, and clients
Participate in team and client meetings as required
Review data management deliverables following documented guidelines
Required Qualifications
Education
Bachelor’s degree or equivalent in life sciences, pharmacy, clinical research, or a related discipline
Experience
3 to 4.6 years of hands-on experience in Clinical Data Management within a CRO or pharmaceutical environment
Prior experience in supporting global clinical trials across multiple phases
Technical Skills
Strong working experience with RAVE and/or Veeva EDC systems
Solid understanding of clinical trial data lifecycle, from study start-up through database lock
Familiarity with regulatory guidelines, SOPs, and client expectations
Core Competencies
Excellent written and verbal communication skills in English
Strong organizational, analytical, and problem-solving abilities
Ability to work independently with minimal supervision in a remote environment
Proven ability to train, guide, and support junior team members
High attention to detail and strong data confidentiality practices
Flexibility to adapt to changing project requirements and timelines
Working Conditions
Fully remote, office-based work environment
Occasional travel to study sites or meetings may be required
Career Growth & Development
This role supports a dedicated FSP client—a globally recognized biopharmaceutical organization with a strong legacy in specialty medicines, vaccines, and scientific innovation. As part of a mature FSP delivery model, you will collaborate with global data science teams and contribute to high-visibility clinical programs.
Thermo Fisher Scientific’s FSP model emphasizes continuous learning through structured career paths, mentorship, and exposure to advanced clinical technologies. Career progression opportunities include Senior Clinical Data Manager, Clinical Data Team Lead, Clinical Data Project Manager, or transition into Data Standards or Programming roles.
Why Join Thermo Fisher Scientific
Work on global, multi-phase clinical trials across diverse therapeutic areas
Gain end-to-end exposure from study setup to database close-out
Build expertise in modern Clinical Data Management, including EDC platforms and AI-enabled workflows
Collaborate with international teams, sponsors, vendors, and CRO partners
Be part of an organization with a strong commitment to scientific excellence and patient impact
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 characteristic protected by law.
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