Clinical Data Management Project Manager (CDM PM) – Fully Remote
Location: Remote, India
Job Type: Full-Time
Category: Clinical Research / Clinical Data Management
Job ID: R-01338265
Work Mode: Fully Remote
Work Schedule: Standard (Monday to Friday)
About the Role
We are seeking an experienced Clinical Data Management Project Manager (CDM PM) to lead and oversee global clinical data management activities across a portfolio of clinical studies. This role is critical to ensuring high-quality, inspection-ready clinical data delivery while maintaining control over scope, timelines, resources, and budgets.
As a CDM PM, you will serve as the primary data management lead and client-facing liaison, providing strategic direction, operational oversight, and leadership to cross-functional teams within a global Functional Service Provider (FSP) model supporting a leading biopharmaceutical sponsor.
Key Responsibilities
Provide leadership, guidance, and coaching to clinical data management teams to ensure timely, accurate, and budget-compliant study delivery
Act as the primary point of contact for clients and internal project stakeholders on all data management-related activities
Independently lead multiple studies or programs, ensuring adherence to regulatory requirements, global SOPs, and client standards
Review, approve, and elevate clinical data management deliverables to ensure inspection readiness and data integrity
Identify, assess, and mitigate project risks related to timelines, quality, scope, and financial performance
Manage project forecasting, resource planning, and budget oversight, including identification and management of out-of-scope activities
Support business development efforts by contributing to bid preparation and participating in bid defense meetings as a data management subject matter expert
Develop, implement, and support process improvements, training initiatives, and best practices within the data management function
Mentor and develop junior and peer-level team members, fostering a high-performance and quality-driven culture
Education and Experience Requirements
Bachelor’s degree in Life Sciences, Pharmacy, Clinical Research, or a related scientific discipline
Minimum 6 to 8 years of progressive experience in Clinical Data Management, including project or program leadership responsibilities
Demonstrated hands-on experience with RAVE and/or Veeva EDC systems
Prior experience managing global, multi-center clinical trials across multiple therapeutic areas is strongly preferred
Required Knowledge, Skills, and Competencies
Strong understanding of global regulatory requirements, GCP, and clinical data management standards
Proven ability to lead and manage data management activities across a portfolio of studies
Excellent written and verbal communication skills with strong stakeholder and client management capabilities
Advanced organizational, analytical, and problem-solving skills with a strong attention to detail
Ability to forecast resources, manage budgets, and ensure adherence to project timelines
Demonstrated capability to identify and mitigate project risks proactively
Strong leadership skills with the ability to train, mentor, delegate, and supervise cross-functional teams
High level of professionalism and ability to maintain confidentiality of clinical and proprietary sponsor data
Career Growth and Development
This role supports a dedicated FSP engagement for a globally recognized biopharmaceutical organization known for its scientific innovation, patient focus, and long-term investment in research and development. As a client-dedicated FSP professional, you will collaborate closely with global data science and clinical operations teams on complex, high-visibility programs.
The FSP model promotes continuous professional development through structured learning pathways, mentorship, and stretch assignments. Career progression opportunities include advancement to Senior CDM Project Manager roles or transitions into Data Standards, Clinical Programming, or Data Strategy functions based on performance and business needs.
Why Join This Opportunity
Gain global exposure by working on international clinical trials across multiple phases and therapeutic areas
Take end-to-end ownership of clinical data management activities from study start-up through close-out
Strengthen project leadership, financial oversight, data quality, and risk management expertise
Build future-ready skills by working with modern EDC platforms, advanced analytics, and AI-enabled clinical trial technologies
About Thermo Fisher Scientific
Thermo Fisher Scientific Inc. is the world leader in serving science, with annual revenues exceeding USD 44 billion. The company’s mission is to enable customers to make the world healthier, cleaner, and safer. Thermo Fisher Scientific supports life sciences research, clinical development, diagnostics, and pharmaceutical manufacturing through its industry-leading portfolio, including Thermo Scientific, Applied Biosystems, Invitrogen, Patheon, Fisher Scientific, Unity Lab Services, and PPD clinical research services.
Thermo Fisher Scientific is an equal opportunity employer committed to diversity, inclusion, and a workplace where all individuals are valued.
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