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Manager, Cdm (Fsp)

Thermo Fisher Scientific
Thermo Fisher Scientific
10+ years
Not Disclosed
10 Dec. 30, 2025
Job Description
Job Type: Full Time 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

Job Title: Manager – Clinical Data Management (FSP)
Location: Bangalore, Karnataka, India (Remote / Fully Remote)
Job Type: Full-time
Category: Clinical Data Management / Clinical Research


About Thermo Fisher Scientific

Thermo Fisher Scientific is a global leader in serving science, enabling customers to make the world healthier, cleaner, and safer. With over 90,000 colleagues and annual revenue exceeding $44 billion, we deliver innovative technologies and pharmaceutical services through trusted brands such as Thermo Scientific, Applied Biosystems, Invitrogen, Fisher Scientific, Unity Lab Services, and Patheon.

Our PPD® clinical research portfolio supports leading pharmaceutical and biotech organizations across 2,700 clinical trials in over 100 countries, providing high-quality, end-to-end clinical data management solutions.


Role Overview

We are seeking an experienced Manager – Clinical Data Management (FSP) to join our global FSP team. This role involves leading a team of project staff, overseeing data management activities, and collaborating with senior management to ensure operational excellence. As a manager, you will drive quality, efficiency, and compliance in all CDM deliverables while mentoring and developing your team for high performance.


Key Responsibilities

  • Lead and manage FSP staff, including recruitment, performance management, mentoring, coaching, and professional development.

  • Oversee project deliverables to ensure accuracy, timeliness, and compliance with client expectations and regulatory requirements.

  • Manage global FSP resource allocation, strategize with senior management, and maintain resourcing reports.

  • Ensure staff compliance with SOPs, regulatory guidelines, and documented procedures.

  • Support operational activities of assigned studies or portfolios with a focus on quality and efficiency.

  • Contribute to the development and implementation of CDM processes, procedures, and training materials.

  • Act as a subject matter expert for DM processes, advising teams on best practices and study-specific strategies.


Education & Experience Requirements

  • Bachelor’s degree in Life Sciences, Pharmacy, Medicine, or a related field; advanced degrees preferred.

  • Experience: 10+ years in Clinical Data Management (CDM) domain.

  • Minimum 2 years of experience managing large, global teams in an FSP or similar business model.

  • Strong working knowledge of FSP operations, global CDM processes, and regulatory requirements.


Required Skills & Competencies

  • Strong organizational and analytical skills with high attention to detail.

  • Excellent written and verbal communication in English.

  • Proficiency in data management systems and clinical trial platforms.

  • Ability to mentor, motivate, and manage high-performing teams.

  • Ability to set and meet deadlines, manage project scope, and adapt to changes in a dynamic environment.

  • High degree of confidentiality with clinical data and proprietary client information.


Why Join Thermo Fisher Scientific

  • Global Exposure: Work on international clinical trials across multiple phases and therapeutic areas, partnering with global teams, CROs, vendors, and country operations.

  • End-to-End Ownership: Engage in all stages of study delivery, from set-up to close-out.

  • Professional Growth: Enhance project management, financial tracking, data analysis, and risk management skills. Gain experience with AI-enabled workflows and advanced clinical trial technologies.

  • Impact: Contribute to life-changing medicines, ensuring patient safety and high-quality data delivery worldwide.


Apply Now: Submit your resume/CV via Thermo Fisher Scientific’s careers portal or through our FSP application process.

Thermo Fisher Scientific is an Equal Opportunity Employer and values diversity, equity, and inclusion in the workplace.