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Manager, Cdm (Fsp)

Thermo Fisher Scientific
Thermo Fisher Scientific
8-12 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

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: 8–12 years clinical research experience, with 3–5 years in supervisory roles


Job Overview

Thermo Fisher Scientific’s PPD Clinical Research Services is seeking a Manager, Clinical Data Management (FSP) to oversee clinical data management activities for global studies. This role combines operational oversight, team leadership, and strategic contribution to ensure high-quality deliverables within a Functional Service Provider (FSP) model.

As a Manager CDM, you will lead and support project staff, collaborate with global teams, manage resource allocation, and ensure compliance with SOPs and client expectations across all assigned studies.


Key Responsibilities

Team & Project Management

  • Supervise FSP staff, including training, mentoring, performance tracking, and workload allocation

  • Approve time records, leave requests, and expenses for direct reports

  • Ensure staff adherence to SOPs, regulatory guidelines, and client-specific requirements

Operational Oversight

  • Manage clinical data management tasks, ensuring accuracy, completeness, and timely delivery

  • Support implementation of EDC systems, AI-based workflows, and quality control procedures

  • Participate in process improvement initiatives to optimize data quality and operational efficiency

Client & Global Collaboration

  • Act as point of contact for clients on data management queries and project deliverables

  • Collaborate with global teams, vendors, and stakeholders to ensure project milestones are met

  • Provide guidance on regulatory compliance, study timelines, and operational risks

Strategic Contribution

  • Support development and refinement of data management processes, procedures, and training programs

  • Ensure alignment of FSP activities with global clinical trial strategies

  • Contribute to quality metrics, audits, and continuous improvement initiatives


Educational & Experience Requirements

Education

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

Experience

  • 8–12 years of clinical research experience, including 3–5 years in supervisory roles

  • Proven experience in FSP or outsourced clinical data management models

  • Strong understanding of global CDM processes, EDC systems, and regulatory compliance

Skills & Competencies

  • Expertise in data management operations, SOPs, and regulatory standards

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

  • Ability to mentor and lead teams to deliver high-quality outputs

  • Proficiency in EDC tools, CTMS, and Microsoft Office

  • Excellent interpersonal, communication, and collaboration skills

  • Ability to manage multiple projects and meet tight deadlines


Why Join Thermo Fisher Scientific – PPD Clinical Research Services

  • Work on global clinical trials across multiple therapeutic areas

  • Lead FSP data management initiatives and implement advanced CDM solutions

  • Gain exposure to AI-enabled data workflows, end-to-end study delivery, and international teams

  • Competitive salary with a comprehensive benefits package

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

  • Contribute to delivering life-changing medicines to patients worldwide