CDM PM (Veeva)
Company: Thermo Fisher Scientific
Location: Bangalore, Karnataka, India (Fully Remote)
Job Type: Full-Time | Remote
Experience: 8+ Years (Clinical Data Management / Project Management)
Qualification: Bachelor’s Degree or equivalent
Salary Range: Not Specified
Job Overview
Thermo Fisher Scientific is seeking a Clinical Data Manager Project Manager (CDM PM) to oversee data management activities across multiple clinical studies.
The role involves managing project deliverables, timelines, and budgets while ensuring high-quality data management processes throughout the clinical trial lifecycle. The position also requires close collaboration with internal teams and clients to ensure efficient study execution and compliance with regulatory guidelines.
This role plays an important part in supporting global clinical research programs through effective data management leadership and operational oversight.
Key Responsibilities
Clinical Data Management Leadership
Manage data management activities across multiple clinical studies or programs.
Provide guidance and coaching to the data management team to ensure deliverables are completed accurately and within timelines.
Act as the primary liaison between project teams and clients.
Lead and delegate tasks to ensure timely completion of project activities.
Project Management & Oversight
Perform the Project Manager role for assigned studies or programs.
Provide functional, administrative, and financial oversight for assigned projects.
Forecast project hours and identify resource requirements.
Manage project budgets and monitor financial performance.
Identify and manage out-of-scope activities and support contract modification processes.
Risk Management & Quality Control
Monitor project progress and identify risks to deliverables and finances.
Develop and implement mitigation strategies to manage project risks.
Ensure deliverables follow Clinical Data Management (CDM) guidelines and quality standards.
Conduct independent reviews of data management deliverables.
Data Management Operations
Support clinical data management processes across studies.
Work with electronic data capture systems including Veeva EDC.
Ensure compliance with regulatory guidelines, global SOPs, and client expectations.
Maintain confidentiality of clinical and proprietary data.
Training & Team Development
Develop and implement study-specific training for data management staff.
Mentor junior staff members and peers across assigned projects.
Provide leadership and direction to study teams.
Support team development and operational excellence in data management processes.
Business Development Support
Participate in proposal and bid preparation activities.
Represent data management in sponsor bid defense meetings when required.
Develop and maintain strong relationships with new and existing clients.
Support initiatives that promote repeat business opportunities.
Required Skills
Clinical Data Management Expertise
Strong experience in clinical data management within clinical trials.
Experience managing multiple studies or programs.
Hands-on experience with Veeva EDC.
Project Management Skills
Experience managing timelines, budgets, and project resources.
Ability to identify and mitigate project risks.
Strong organizational and analytical problem-solving skills.
Communication & Leadership
Excellent written and verbal communication skills.
Strong stakeholder and client management abilities.
Ability to lead teams, delegate responsibilities, and mentor staff.
Technical & Operational Knowledge
Understanding of regulatory guidelines and global SOPs.
Ability to use interactive computer systems and data management platforms.
Strong ability to manage clinical data confidentiality and compliance requirements.
Preferred Qualifications
Advanced experience in Clinical Data Management Project Management.
Experience working in a Contract Research Organization (CRO) environment.
Experience supporting global clinical trials.
Knowledge of project forecasting and resource planning.
Key Competencies
Clinical Data Management and project oversight
Veeva EDC system expertise
Clinical trial operations and regulatory compliance
Project planning, budgeting and forecasting
Risk management and quality control
Team leadership and mentoring
Client relationship management
About the Company
Thermo Fisher Scientific is a global leader in scientific research services and life sciences solutions. Through its clinical research portfolio including PPD, the company supports pharmaceutical and biotechnology organizations in advancing drug development and clinical trials worldwide. Over the past five years, the organization has supported more than 2,700 clinical trials across over 100 countries, helping bring innovative therapies to patients around the world.
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