Clinical Data Management Project Manager (CDM PM – FSP)
Company: Thermo Fisher Scientific – PPD Clinical Research Services
Location: Remote, India
Job Type: Full-Time / Fully Remote
Category: Clinical Research / Clinical Data Management
Experience Required: 6–8 years in Clinical Data Management or CDM Project Management
Job Overview
Thermo Fisher Scientific’s PPD Clinical Research Services is seeking a Clinical Data Management Project Manager (CDM PM) to join our global FSP team. In this role, you will lead a portfolio of clinical studies or programs, overseeing functional, administrative, and financial aspects from start-up to close-out.
You will act as the primary liaison between clients and cross-functional teams, coach and mentor CDM staff, manage budgets and resources, mitigate risks, and ensure the delivery of high-quality, inspection-ready clinical data. This role provides exposure to global study operations, EDC platforms, and data-driven study management.
Key Responsibilities
Project & Team Leadership
Lead and mentor CDM teams, providing coaching, guidance, and direction to ensure timely, accurate, and quality delivery
Serve as primary contact for clients and cross-functional teams, maintaining strong communication and stakeholder engagement
Develop and implement study-specific training for CDM staff
Operational & Functional Oversight
Monitor study deliverables, identify risks, and implement mitigation strategies to maintain timelines, budgets, and scope
Review, approve, and elevate CDM outputs, ensuring compliance with internal SOPs, client standards, and regulatory requirements
Forecast project resourcing needs and manage project budgets, including identification and management of out-of-scope activities
Process Improvement & Business Development Support
Drive continuous improvement initiatives within CDM processes and procedures
Support business development by contributing to bid preparation, client presentations, and proposal reviews
Promote repeat business through client relationship management and high-quality service delivery
Regulatory & Technical Oversight
Ensure all clinical data management deliverables meet inspection readiness and regulatory compliance standards
Utilize EDC systems (RAVE, Veeva, or equivalent) for data validation, tracking, and reporting
Qualifications & Experience
Education:
Bachelor’s degree in Life Sciences, Pharmacy, Nursing, or related field
Experience:
6–8 years of experience in Clinical Data Management or CDM Project Management
Experience with EDC platforms (RAVE, Veeva, or equivalent)
Demonstrated experience managing teams, study deliverables, budgets, and global stakeholders
Prior FSP or CRO experience preferred
Skills & Competencies:
Strong project management and organizational skills
Excellent written and verbal communication, with professional command of English
Proficiency in clinical trial systems, data management workflows, and regulatory guidelines
Ability to mentor and lead teams, delegate tasks effectively, and resolve operational challenges
Analytical mindset with strong risk identification and mitigation skills
Ability to work remotely and collaboratively with global teams
Career Growth & Global Exposure
Work across global clinical studies in multiple therapeutic areas and phases
Gain experience with AI-enabled clinical trial technologies and modern CDM workflows
Opportunities to advance into Senior CDM PM, Data Standards, or Clinical Data Leadership roles
Hands-on exposure to study delivery, operational strategy, and budget management
Why Join Thermo Fisher Scientific – PPD Clinical Research Services
Global Reach: Collaborate with international teams, CROs, vendors, and country operations
End-to-End Ownership: Contribute to every stage of study delivery, from setup to close-out
Innovation & Technology: Leverage modern CDM platforms and AI-driven solutions for trial data management
Career Development: Structured mentorship, stretch assignments, and FSP-focused career paths
Collaborative Environment: Join a team committed to quality, operational excellence, and patient impact
Gujarat :
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Siliguri |Illinois :
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