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Cdm Pm

Thermo Fisher Scientific
Thermo Fisher Scientific
6-8 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

Clinical Data Manager – Project Manager (CDM PM) – Remote, India

Job ID: R-01338265
Job Type: Full-Time
Category: Clinical Research / Clinical Data Management
Work Mode: Fully Remote
Location: India

About the Role

Thermo Fisher Scientific is seeking a Clinical Data Manager Project Manager (CDM PM) to lead a portfolio of studies within our Functional Service Provider (FSP) model. In this role, you will provide strategic oversight across data management activities, ensuring high-quality deliverables while managing timelines, budgets, and resources. You will serve as the primary liaison to clients and cross-functional teams, mentoring CDM staff and implementing process improvements that drive inspection-ready outcomes.

This position offers the opportunity to work with global data teams, supporting top pharmaceutical and biotechnology sponsors across multiple therapeutic areas, while shaping the end-to-end clinical data management process.

Key Responsibilities

  • Lead and oversee a portfolio of clinical trials, ensuring all data management deliverables are completed on time, within scope, quality standards, and budget

  • Coach, mentor, and direct CDM staff, providing guidance and training on best practices, SOPs, and regulatory requirements

  • Serve as the primary liaison to clients, cross-functional teams, and project leadership

  • Monitor project timelines, budgets, and resources; identify risks and implement mitigation strategies

  • Conduct independent reviews of DM deliverables to ensure compliance with global SOPs and study protocols

  • Support business development initiatives, including bid preparation, client meetings, and fostering repeat business relationships

  • Participate in process improvement, procedural updates, and departmental training initiatives

  • Delegate and manage tasks across multiple studies, ensuring effective coordination and timely delivery

Education & Experience Requirements

  • Bachelor’s degree in Life Sciences, Pharmacy, Biotechnology, or related field

  • 6–8 years of relevant experience in Clinical Data Management, with a minimum of hands-on experience in RAVE or Veeva EDC

  • Proven experience in managing cross-functional teams and complex study portfolios

Knowledge, Skills & Competencies

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

  • Excellent analytical, problem-solving, and organizational skills

  • Exceptional written and verbal communication skills, with a strong command of English

  • Ability to identify project risks and develop effective mitigation plans

  • Expertise in team leadership, mentoring, and performance management

  • High degree of confidentiality, integrity, and professionalism in handling clinical data

  • Ability to manage budgets, forecast resources, and oversee project timelines across multiple studies

  • Proficiency in interactive software and clinical data management systems

Career Growth Opportunities

As part of Thermo Fisher Scientific’s FSP Data Management team, CDM PMs have access to:

  • Global exposure: Work on international clinical trials, collaborating with CROs, sponsors, and country teams

  • End-to-end ownership: Contribute to all stages of study delivery, from start-up to database lock and close-out

  • Skill expansion: Learn modern clinical trial technologies, including AI-enabled CDM platforms

  • Career advancement: Progress along the CDM track (Senior CDM PM, CDM Director) or explore Data Standards/Programming roles

Why Join Thermo Fisher Scientific

Join a leading global contract research organization that has supported over 2,700 clinical trials across 100+ countries. Be part of a team that delivers life-changing medicines to patients worldwide while accelerating your professional growth in a collaborative, innovative environment.

About Thermo Fisher Scientific:
Thermo Fisher Scientific Inc. is a world leader in serving science, with annual revenue exceeding $44 billion. Our mission is to enable our customers to make the world healthier, cleaner, and safer. With over 90,000 colleagues worldwide, we provide innovative technologies, laboratory services, and global expertise through leading brands, including Thermo Scientific, Applied Biosystems, Invitrogen, Fisher Scientific, Unity Lab Services, and Patheon.

Learn more at www.thermofisher.com. Thermo Fisher Scientific is an Equal Opportunity Employer.