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Manager, Cdm (Fsp)

Thermo Fisher Scientific
Thermo Fisher Scientific
10+ years
Not Disclosed
10 Jan. 1, 2026
Job Description
Job Type: Full Time Remote Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Manager – Clinical Data Management (FSP)

Company: Thermo Fisher Scientific
Job Type: Full-Time, Fully Remote
Location: Bangalore, Karnataka, India
Experience: 10+ years in CDM, 2+ years managing global teams
Category: Clinical Research / Data Management


About Thermo Fisher Scientific

Thermo Fisher Scientific is a world 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 advance scientific discovery and improve patient outcomes.

Learn more: www.thermofisher.com


Role Overview

The Manager, Clinical Data Management (FSP) will lead and oversee a global team of data management professionals within our Functional Service Provider (FSP) model. This role involves team management, operational oversight, project delivery, and strategic planning to ensure high-quality clinical data management and client satisfaction.

As a manager, you will mentor, coach, and guide direct reports while partnering with senior management to align resources and processes with business objectives.


Key Responsibilities

  • Team Leadership & Management:

    • Manage FSP staff, including recruitment, onboarding, performance management, goal-setting, professional development, coaching, and counseling.

    • Approve time records, expense reports, leave requests, and overtime.

    • Guide staff to ensure accuracy, timeliness, and quality in data management deliverables.

  • Operational Oversight:

    • Support study teams in CDM operations and ensure adherence to SOPs, GCP, and client expectations.

    • Oversee FSP resourcing, allocation, and global reporting.

    • Participate in the development and implementation of CDM processes, procedures, and training programs.

  • Project & Client Management:

    • Act as the study expert for DM processes and workflows.

    • Collaborate with cross-functional teams to manage study delivery, timelines, and quality standards.

    • Monitor budgets, performance metrics, and risk management strategies.


Qualifications & Skills

  • Education: Bachelor’s degree or equivalent; advanced degrees preferred.

  • Experience:

    • 10+ years in Clinical Data Management domain.

    • 2+ years managing large global teams.

    • Strong experience in FSP business model operations.

  • Technical & Analytical Skills:

    • Expertise in CDM processes, EDC systems, and 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 team members effectively.

    • Excellent written and verbal communication in English.

  • Additional Competencies:

    • Detail-oriented, highly organized, and able to maintain confidentiality.

    • Ability to manage timelines, prioritize tasks, and adapt to changing project demands.


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 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.