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Manager, Cdm (Fsp)

Thermo Fisher Scientific
Thermo Fisher Scientific
2-10+ years
preferred by company
10 Jan. 9, 2026
Job Description
Job Type: Full Time Remote Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ 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)

Job ID: R-01338083
Job Type: Full-Time
Category: Clinical Research / Clinical Data Management
Work Mode: Fully Remote
Shift: Second Shift (Afternoons)
Location: Bangalore, Karnataka, India

Job Overview

A leading global Contract Research Organization (CRO) within the PPD® Clinical Research portfolio at Thermo Fisher Scientific is seeking an experienced Manager, Clinical Data Management (FSP) to lead and support global Functional Service Provider (FSP) data management teams.

This leadership role is ideal for a seasoned Clinical Data Management professional with deep expertise in the FSP operating model, strong people management capabilities, and a proven ability to deliver high-quality data management services across complex, global clinical trial portfolios.

Key Responsibilities

  • Lead, manage, and develop FSP Clinical Data Management teams, including recruitment, onboarding, performance management, coaching, mentoring, and professional development

  • Oversee workload planning, task allocation, and utilization for direct reports to ensure timely and high-quality project delivery

  • Partner with senior management to drive training initiatives, career development, and performance excellence across the FSP CDM organization

  • Manage global resource planning, allocation, and capacity reporting for assigned FSP staff and portfolios

  • Ensure compliance with SOPs, regulatory requirements, client standards, and quality expectations

  • Provide operational oversight and coaching to portfolio teams to ensure tasks are delivered accurately, on time, and within budget

  • Support study and portfolio-level operational activities with a strong focus on data quality, risk mitigation, and continuous improvement

  • Collaborate with study managers, sponsors, and cross-functional stakeholders to optimize data management execution

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

  • Act as a subject matter expert for Clinical Data Management processes, systems, and FSP delivery models

Required Education & Experience

  • Bachelor’s degree in Life Sciences, Pharmacy, Biostatistics, Computer Science, or a related discipline

  • Minimum 10+ years of experience in the Clinical Data Management domain (mandatory)

  • At least 2+ years of experience managing large, global teams within a CRO or sponsor environment

  • Proven hands-on experience working within a Functional Service Provider (FSP) business model

  • Equivalent combinations of education, formal training, and directly related experience may be considered

Required Skills & Competencies

  • Strong understanding of clinical trial data management processes, regulatory guidelines, and global SOPs

  • Ability to effectively apply CDM knowledge while meeting client, regulatory, and quality expectations

  • High attention to detail with strong numerical and analytical skills

  • Excellent written and verbal communication skills with a strong command of the English language

  • Strong problem-solving, risk management, and decision-making abilities

  • Demonstrated ability to manage confidential clinical and proprietary data with integrity

  • Strong interpersonal and stakeholder management skills across global teams

  • Proven leadership capability to motivate, coach, and supervise diverse teams

  • Ability to delegate effectively while maintaining accountability and quality oversight

  • Strong time management skills with the ability to set, monitor, and adjust timelines in response to project demands

Why Join the FSP Clinical Data Management Team

  • Work on global, high-impact clinical trials across multiple therapeutic areas and phases

  • Gain exposure to international sponsors, CRO partners, vendors, and country operations

  • Lead end-to-end data management delivery from study start-up through database lock and close-out

  • Strengthen global project management, financial oversight, and risk management expertise

  • Build experience with modern CDM technologies, including EDC platforms, data quality tools, and AI-enabled clinical trial workflows

  • Be part of a collaborative, innovation-driven environment focused on patient impact and scientific excellence

About Thermo Fisher Scientific

Thermo Fisher Scientific Inc. is a global leader in serving science, with annual revenues exceeding USD 44 billion. Through its PPD® Clinical Research Services, Thermo Fisher Scientific delivers comprehensive clinical development solutions that accelerate the delivery of life-changing therapies worldwide.

Thermo Fisher Scientific is an equal opportunity employer committed to diversity, equity, and inclusion.