CDM PM

Roles & Responsibilities:

• Lead and manage a portfolio of clinical studies from start-up through close-out
• Act as primary liaison between clients, project teams, and cross-functional stakeholders
• Provide coaching and oversight to CDM teams to ensure quality, timelines, and budget adherence
• Review and approve data management deliverables per CDM guidelines and SOPs
• Identify project risks and implement mitigation strategies for deliverables and finances
• Forecast resources, timelines, and manage study budgets including out-of-scope activities
• Support bid preparation, bid defense meetings, and client development initiatives
• Drive process improvement, training, and best practices within data management
• Ensure compliance with regulatory requirements, GCP, and global SOPs
• Maintain inspection-ready status across assigned studies

Qualification:

• Bachelor’s degree or equivalent in a relevant discipline

Experience:

• 6–8 years of experience in Clinical Data Management
• Hands-on experience with RAVE / Veeva EDC
• Experience managing multiple global clinical trials

Skills:

• Strong understanding of CDM processes and regulatory requirements
• Excellent project management, budgeting, and forecasting skills
• Ability to lead, mentor, and train study teams
• Strong analytical, organizational, and problem-solving abilities
• Excellent written and verbal communication skills
• Ability to manage confidential clinical and proprietary data
• Experience working in global, matrix, client-facing environments

About The Organization:

Thermo Fisher Scientific is a global leader in life sciences and clinical research, with annual revenue exceeding $44 billion and a workforce of over 90,000 employees. The company supports 2,700+ clinical trials across 100+ countries, enabling customers to make the world healthier, cleaner, and safer.