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Sr. Manager, Cdm (Fsp)

Thermo Fisher Scientific
Thermo Fisher Scientific
12+ years
Not Disclosed
10 Jan. 20, 2026
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

Senior Manager – Clinical Data Management (FSP)

Company: Thermo Fisher Scientific – PPD Clinical Research Services
Location: Bangalore, Karnataka, India
Job Type: Full-Time / Fully Remote
Category: Clinical Data Management / FSP
Experience Required: 12+ years clinical research experience, with 5+ years in leadership roles


Job Overview

Thermo Fisher Scientific’s PPD Clinical Research Services is seeking a Senior Manager, Clinical Data Management (FSP) to lead a high-performing team supporting global clinical trials. This role offers strategic oversight of clinical data management activities, team leadership, and operational excellence within a Functional Service Provider (FSP) model.

As a Senior Manager CDM, you will be responsible for managing FSP staff, overseeing resourcing, ensuring quality deliverables, and mentoring project teams. You will collaborate closely with global leadership and client teams to support complex, high-visibility clinical studies across multiple therapeutic areas.


Key Responsibilities

Team & Leadership Management

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

  • Approve staffing allocations, time records, expense reports, and leave requests

  • Set goals, monitor performance, and ensure staff compliance with SOPs, regulatory requirements, and client expectations

Operational Oversight

  • Provide guidance to ensure timely, accurate, and budget-compliant completion of study tasks

  • Oversee resourcing for assigned staff and provide global resourcing reports and strategic recommendations

  • Participate in implementing and refining CDM processes, procedures, and training for the data management function

  • Ensure high-quality clinical data management deliverables throughout the study lifecycle

Client & Project Collaboration

  • Act as study expert on data management processes for the portfolio

  • Provide oversight for global and local teams, CROs, and vendors within FSP delivery models

  • Support operational activities across study portfolios to optimize data quality, timelines, and regulatory compliance

Strategic Contributions

  • Contribute to process improvement initiatives, operational excellence, and training programs

  • Support adoption of modern CDM technologies, including AI-enabled platforms, EDC systems, and global study delivery tools


Educational & Experience Requirements

Education

  • Bachelor’s degree in Life Sciences, Computer Science, Statistics, or a related discipline (Master’s preferred)

Experience

  • 12+ years of clinical research experience, with 5+ years in a leadership role

  • Proven experience in FSP or outsourced clinical data management models

  • Expertise in managing global teams, budgets, and operational priorities

Skills & Competencies

  • Strong knowledge of clinical data management processes, SOPs, and regulatory requirements

  • Ability to manage, mentor, and motivate teams while maintaining accountability and quality

  • Excellent analytical, problem-solving, and project management skills

  • High proficiency in EDC systems, data quality tools, and Microsoft Office

  • Strong interpersonal, verbal, and written communication skills

  • Ability to manage multiple projects, timelines, and deliverables in a fast-paced environment

  • Maintain confidentiality of clinical and proprietary data


Why Join Thermo Fisher Scientific – PPD Clinical Research Services

  • Lead global FSP data management initiatives for top-tier biopharmaceutical clients

  • Gain hands-on experience in advanced CDM technologies, AI-enabled workflows, and end-to-end study delivery

  • Collaborate with international teams, vendors, and stakeholders across therapeutic areas

  • Competitive salary and comprehensive benefits package

  • Opportunities for career growth and leadership development in a global CRO environment

  • Contribute to delivering life-changing medicines to patients worldwide