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Manager, Cdm (Fsp)

Thermo Fisher Scientific
Thermo Fisher Scientific
2-10 years
Not Disclosed
10 Jan. 1, 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

Job Title: Manager, Clinical Data Management (FSP)
Category: Clinical Research / Data Management
Location: Bangalore, Karnataka, India (Fully Remote Option Available)
Job Type: Full-Time
Job ID: R-01338083


About the Role

Thermo Fisher Scientific is seeking an experienced Manager in Clinical Data Management (FSP) to join our global clinical research services team. As a leader in the contract research organization (CRO) sector, we support top pharmaceutical companies and over 750 biotech organizations across 2,700+ clinical trials in 100+ countries.

In this role, you will manage a team of project staff, oversee workload distribution, and ensure high-quality, timely clinical data management across multiple studies. You will also collaborate with senior management to mentor, guide, and develop your team, driving excellence in Clinical Data Management (CDM) operations.


Key Responsibilities

  • Manage and mentor FSP staff, including hiring, performance management, goal setting, professional development, and career growth.

  • Oversee staff allocations and global resourcing strategies, ensuring efficient utilization across projects.

  • Provide guidance and coaching to portfolio teams to ensure tasks are completed accurately, on time, and within budget.

  • Ensure compliance with internal SOPs, client requirements, and regulatory guidelines.

  • Support operational activities for studies and portfolios with a focus on quality and efficiency.

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

  • Act as a subject matter expert for data management processes, advising on best practices and process improvements.

  • Maintain confidentiality of clinical trial data and proprietary client information.


Required Qualifications & Experience

  • Education: Bachelor’s degree or equivalent; formal academic or vocational qualification in relevant field.

  • Experience:

    • Minimum 10 years in Clinical Data Management

    • At least 2 years managing large global teams

    • Hands-on experience with Functional Service Provider (FSP) model

  • Strong knowledge of CDM operations, regulatory compliance, and data quality standards.

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

  • Effective written and verbal communication skills in English.

  • Ability to motivate and supervise teams, delegate tasks, and manage timelines.


Preferred Skills

  • Expertise in EDC systems, AI-enabled workflows, and global clinical trial technologies.

  • Experience in multi-phase international clinical studies across therapeutic areas.

  • Strong financial tracking, risk management, and data analysis capabilities.