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Manager, Cdm (Fsp)

Thermo Fisher Scientific
Thermo Fisher Scientific
2+10 years
Not Disclosed
Bangalore, India
10 Feb. 16, 2026
Job Description
Job Type: Full Time 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)

Company: Thermo Fisher Scientific
Location: Bangalore (Fully Remote)
Job Type: Full-Time
Category: Clinical Research / Clinical Data Management
Work Schedule: Second Shift (Afternoon Hours)

Job Overview
Thermo Fisher Scientific is hiring an experienced Manager, Clinical Data Management (FSP) to lead global clinical data management operations within its Functional Service Provider (FSP) model. This leadership role involves managing project teams, overseeing clinical data management processes, ensuring regulatory compliance, and supporting global clinical trials.

The position offers an opportunity to work with leading pharmaceutical and biotechnology companies, contributing to clinical research initiatives that accelerate drug development and improve patient outcomes worldwide.

Key Responsibilities

Team Leadership and Staff Management

  • Manage and supervise FSP clinical data management staff, including hiring, onboarding, performance management, and professional development.

  • Provide coaching, mentoring, and guidance to project teams and direct reports.

  • Conduct performance evaluations, manage salary administration, and oversee employee engagement activities.

  • Review and approve time records, expense reports, and leave requests.

Operational Oversight and Project Execution

  • Provide strategic oversight and support to ensure timely, accurate, and high-quality project delivery.

  • Manage staff workload allocation and global resource planning for assigned projects.

  • Ensure team compliance with established procedures, regulatory guidelines, and organizational standards.

  • Support operational activities across study portfolios with a strong focus on quality and efficiency.

  • Collaborate with study managers and senior leadership to optimize project execution.

Process Improvement and Compliance

  • Participate in the development and implementation of clinical data management processes and standard operating procedures.

  • Ensure adherence to regulatory requirements, global SOPs, and client expectations.

  • Maintain confidentiality of clinical data and proprietary client information.

  • Identify opportunities to improve operational workflows and data management practices.

Strategic Collaboration

  • Partner with senior management to support training initiatives and workforce planning.

  • Contribute to global resourcing strategies and reporting.

  • Ensure alignment of team deliverables with organizational and client objectives.

Education Requirements

  • Bachelor’s degree or equivalent qualification in Life Sciences, Pharmacy, Biotechnology, Clinical Research, or a related discipline.

  • Equivalent combinations of education, training, and relevant experience may be considered.

Experience Required

  • Minimum 10 years of experience in the Clinical Data Management domain.

  • At least 2 years of experience managing large global teams.

  • Strong experience working within the Functional Service Provider (FSP) business model.

  • Proven experience in clinical trial data management operations and project oversight.

Required Skills and Competencies

  • Strong understanding of clinical data management processes and regulatory frameworks.

  • Excellent leadership and team management capabilities.

  • Strong organizational and project management skills.

  • High attention to detail and strong numerical aptitude.

  • Excellent written and verbal communication skills in English.

  • Strong analytical and problem-solving abilities.

  • Ability to manage multiple priorities and meet project timelines.

  • Strong interpersonal skills and ability to collaborate with cross-functional teams.

  • Ability to supervise, motivate, and delegate tasks effectively.

Work Environment

  • Office-based work environment with remote working flexibility.

  • Standard office conditions with exposure to electronic equipment.

Career Growth and Benefits

  • Opportunity to work on global clinical studies across multiple therapeutic areas.

  • Exposure to international clinical trial operations and cross-functional collaboration.

  • End-to-end involvement in clinical study delivery from initiation to close-out.

  • Professional development in clinical trial technologies, data analytics, and AI-enabled workflows.

  • Experience in global project management, financial tracking, and risk management.