CDM Project Manager (Veeva) – Clinical Data Management
Company: Thermo Fisher Scientific
Location: Bangalore (Fully Remote)
Job Type: Full-Time
Category: Clinical Research / Clinical Data Management
Job Overview
Thermo Fisher Scientific is seeking an experienced Clinical Data Manager Project Manager (CDM PM – Veeva) to lead and manage clinical data management projects within its global clinical research services division. The role involves overseeing multiple clinical studies, ensuring data quality, maintaining regulatory compliance, and driving operational excellence across project deliverables.
This position offers the opportunity to work with global pharmaceutical and biotechnology clients, supporting clinical trials and contributing to the development of innovative therapies that address critical healthcare challenges worldwide.
Key Responsibilities
Operational and Project Management
Manage and oversee multiple clinical data management studies independently or as part of a program.
Provide functional, administrative, and financial oversight of assigned projects.
Ensure timely delivery of high-quality project outcomes within scope and budget.
Monitor project timelines, resource allocation, and deliverables to maintain operational efficiency.
Identify project risks and implement mitigation strategies to ensure successful study execution.
Stakeholder Management and Client Engagement
Act as the primary liaison between project teams and clients.
Build and maintain strong relationships with internal and external stakeholders.
Support business development activities including bid preparation and client presentations.
Promote repeat business through effective client engagement and service excellence.
Team Leadership and Development
Provide guidance, coaching, and mentoring to data management teams.
Deliver study-specific training to project staff.
Review data management deliverables to ensure compliance with established standards.
Lead, supervise, and delegate tasks to ensure efficient project execution.
Quality, Compliance, and Process Improvement
Ensure adherence to regulatory guidelines, global SOPs, and client requirements.
Support development and implementation of data management processes and procedures.
Identify opportunities for process improvement and operational efficiency.
Maintain confidentiality of clinical and proprietary client data.
Financial and Resource Management
Forecast project timelines and resource requirements.
Manage project budgets and identify out-of-scope activities.
Participate in contract modification processes and financial planning activities.
Education Requirements
Bachelor’s degree or equivalent in Life Sciences, Clinical Research, Pharmacy, Biotechnology, or related discipline.
Equivalent combinations of education, training, and relevant experience may be considered.
Experience Required
Minimum 8 years of experience in Clinical Data Management.
Proven experience in project management within clinical data management environments.
Hands-on experience working with Veeva EDC systems.
Experience managing multiple clinical studies or programs preferred.
Required Skills and Competencies
Strong understanding of clinical data management processes and regulatory standards.
Excellent project management and organizational skills.
Strong analytical and problem-solving capabilities.
Excellent written and verbal communication skills in English.
Ability to lead cross-functional teams and mentor junior staff.
Strong risk assessment and mitigation planning abilities.
Proficiency in project forecasting, resource planning, and budget management.
Ability to work independently and manage multiple priorities effectively.
Work Environment
Office-based work environment with standard working schedule (Monday to Friday).
Occasional domestic and international travel may be required.
Uttar Pradesh :
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