CDM Project Manager (Veeva) – Clinical Data Management
Location: Bangalore, Karnataka, India
Job ID: R-01341187
Job Type: Full-Time
Category: Clinical Research
Work Mode: Fully Remote
Work Schedule: Standard (Monday–Friday)
Work Environment: Office-Based
Job Overview
A leading global clinical research organization under Thermo Fisher Scientific is hiring a Clinical Data Management (CDM) Project Manager with strong expertise in Veeva EDC. This role is responsible for managing clinical data management projects, overseeing multiple studies, and ensuring operational excellence across clinical research programs.
The CDM Project Manager will provide strategic, functional, and financial oversight of assigned projects, manage cross-functional teams, ensure regulatory compliance, and drive high-quality data management deliverables within defined timelines and budgets.
Key Responsibilities
Act as a study manager for individual or multiple clinical studies or program portfolios.
Provide leadership, support, and coaching to data management teams to ensure project deliverables are completed accurately, on time, and within budget.
Serve as the primary liaison between project teams and clients, ensuring effective communication and alignment.
Develop and implement study-specific training programs for data management project staff.
Conduct independent reviews of clinical data management deliverables in accordance with CDM guidelines.
Monitor project risks and implement mitigation strategies to ensure timely and successful project execution.
Support business development initiatives, including bid preparation and participation in bid defense meetings.
Build and maintain strong relationships with new and existing clients to promote long-term collaboration and repeat business.
Perform project forecasting, resource planning, and budget management, including identification of out-of-scope work and contract modification processes.
Contribute to the development and implementation of data management processes, procedures, and training programs.
Mentor junior team members and provide leadership across study activities.
Lead and delegate project tasks to ensure compliance with timelines, quality standards, and budget requirements.
Technical Skills and Competencies
Strong hands-on experience with Veeva EDC and clinical data management systems.
Proven expertise in data management project management activities within clinical research.
In-depth understanding of regulatory requirements, global standard operating procedures, and clinical data standards.
Strong project risk identification and mitigation capabilities.
Excellent written and verbal communication skills with strong command of professional documentation standards.
Strong analytical, organizational, and problem-solving abilities.
Ability to manage confidential clinical and proprietary data.
Expertise in project forecasting, resource planning, and timeline management.
Leadership skills with the ability to supervise, train, and guide cross-functional teams.
Customer-focused mindset with strong interpersonal and stakeholder management skills.
Educational Qualifications and Experience Required
Bachelor’s degree or equivalent academic or vocational qualification in life sciences, clinical research, or a related discipline.
Minimum 8+ years of experience in clinical data management roles.
Demonstrated hands-on experience in Veeva EDC and clinical data management project leadership.
Proven experience managing multiple clinical studies or data management programs.
Equivalent combinations of education, training, and relevant experience may be considered.
Working Conditions
Work performed in an office-based environment with standard office equipment.
Occasional travel to site locations, including domestic and international travel, may be required.
Uttar Pradesh :
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