Sr. Manager – Clinical Data Management (FSP)
Company: Thermo Fisher Scientific
Job Type: Full-Time, Fully Remote
Location: Bangalore, Karnataka, India
Experience: 12+ years in CDM, 5+ years in leadership roles
Category: Clinical Research / Data Management
About Thermo Fisher Scientific
Thermo Fisher Scientific is a global leader in serving science, with a mission to enable customers to make the world healthier, cleaner, and safer. With over 90,000 employees worldwide and annual revenue exceeding $44 billion, we provide innovative technologies, life sciences research solutions, and clinical services that accelerate scientific discovery and improve patient outcomes.
Learn more: www.thermofisher.com
Role Overview
The Sr. Manager, Clinical Data Management (FSP) will oversee a global team of clinical data management professionals, ensuring high-quality, compliant, and timely delivery across multiple clinical trials. This role combines strategic leadership, team management, and operational oversight within the FSP model to drive efficiency, quality, and client satisfaction.
You will mentor and guide managers and team leads, manage global resourcing, and act as a subject-matter expert for CDM processes, contributing to the continuous improvement of operational workflows.
Key Responsibilities
Team Leadership & People Management:
Lead FSP staff, including recruitment, performance management, coaching, mentoring, professional development, and succession planning.
Approve HR-related activities such as leave, expenses, overtime, salary decisions, and corrective actions.
Provide guidance to ensure project tasks are completed accurately, on time, and within budget.
Operational & Strategic Oversight:
Manage resource allocations across global studies and ensure adherence to SOPs, GCP, and client expectations.
Assist in implementing operational activities for study portfolios with a focus on quality and efficiency.
Contribute to process development, standardization, and training initiatives within CDM.
Project & Client Management:
Act as the study expert for DM processes and workflows.
Collaborate with cross-functional and client teams to oversee study delivery, risk management, and data quality.
Ensure inspection-ready study data and adherence to global regulatory standards.
Qualifications & Skills
Education: Bachelor’s degree or equivalent; advanced degrees preferred.
Experience:
12+ years in Clinical Data Management domain.
5+ years in leadership roles managing global teams.
Strong experience in FSP business model operations.
Technical & Analytical Skills:
Expertise in CDM processes, EDC systems, and global clinical trial workflows.
Strong analytical, problem-solving, and project management skills.
Leadership & Communication Skills:
Excellent interpersonal, organizational, and leadership abilities.
Ability to supervise, delegate, and motivate multiple layers of team members effectively.
Excellent written and verbal communication in English.
Additional Competencies:
Detail-oriented, highly organized, and able to maintain confidentiality.
Ability to adapt to changing priorities and drive operational excellence.
Why Join Thermo Fisher Scientific?
Global Exposure: Work on international clinical trials across therapeutic areas and phases.
End-to-End Ownership: Contribute to study delivery from start to close-out.
Professional Growth: Strengthen leadership, project management, financial tracking, data analysis, and risk management skills.
Innovation: Gain hands-on experience with AI-enabled CDM workflows and cutting-edge clinical trial technologies.
Gujarat :
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Rangpo |India :
Siliguri |Illinois :
Abbott Park | Bloomingdale | Champaign | Chicago | Deerfield | Glenview | Lake Forest | Lombard | Naperville | Norridge | Park RIdge | Round Lake |Maryland :
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