Welcome Back

Google icon Sign in with Google
OR
I agree to abide by Pharmadaily Terms of Service and its Privacy Policy

Create Account

Google icon Sign up with Google
OR
By signing up, you agree to our Terms of Service and Privacy Policy
Instagram
youtube
Facebook

Cdm Pm

Thermo Fisher Scientific
Thermo Fisher Scientific
6-8 years
Not Disclosed
10 Dec. 30, 2025
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

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

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


About the Role

Thermo Fisher Scientific’s Clinical Research Services (CRS) team leads innovation in global clinical trials, supporting over 2,700 studies across 100+ countries for top pharmaceutical and biotechnology companies. We are seeking an experienced Clinical Data Manager – Project Manager (CDM PM) to oversee a portfolio of clinical studies, ensuring end-to-end project delivery, data quality, compliance, and client satisfaction. This is a fully remote role within India, offering exposure to global clinical research operations.


Key Responsibilities

  • Lead and manage a portfolio of clinical studies or programs from start-up to close-out, overseeing functional, administrative, and financial aspects.

  • Serve as the primary liaison between clients and cross-functional teams, ensuring deliverables meet scope, quality, timeline, and budget.

  • Provide guidance, training, and mentorship to CDM staff, supporting professional development and inspection-ready outcomes.

  • Monitor project risks, develop mitigation strategies, and ensure adherence to SOPs, GCP, and regulatory guidelines.

  • Review and approve CDM deliverables, ensuring accuracy, consistency, and compliance with project-specific requirements.

  • Support business development by assisting with bid preparation and representing CDM in client meetings.

  • Perform project forecasting of hours and resources, manage budgets, and identify out-of-scope work requiring contract modifications.

  • Contribute to process improvement initiatives, SOP development, and training for the data management function.


Education & Experience Requirements

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

  • 6 to 8 years of relevant experience in Clinical Data Management, including project management responsibilities.

  • Hands-on experience with RAVE / Veeva EDC or similar electronic data capture systems.

  • Proven expertise in clinical trial data review, management, and quality assurance.


Skills & Competencies

  • Strong knowledge of clinical trial processes, data management standards, and regulatory compliance.

  • Excellent written and verbal communication skills with a strong command of English.

  • Analytical mindset with strong problem-solving, organizational, and project management skills.

  • Ability to mentor and direct study teams, providing leadership across multiple studies.

  • Proficient in forecasting resources, planning project timelines, and budget management.

  • Ability to maintain confidentiality of clinical data and client proprietary information.

  • Adaptable, collaborative, and able to work independently or in a team environment.


Career Growth & Opportunities

As part of a Functional Service Provider (FSP) model, you will support a globally recognized biopharmaceutical sponsor specializing in specialty medicines, vaccines, and scientific innovation. Benefits include:

  • Exposure to global clinical trials across therapeutic areas and phases.

  • End-to-end involvement in study delivery, from CRF design to database close-out.

  • Hands-on experience with modern CDM tools, AI-enabled workflows, and global data analytics.

  • Career progression opportunities to Senior CDM PM, CDTL, or Data Standards/Programming roles based on skill, performance, and business needs.

  • Collaborate with international teams, CROs, and vendors, enhancing global clinical research expertise.


Why Join Thermo Fisher Scientific

  • Global Impact: Contribute to life-changing medicines reaching patients worldwide.

  • Professional Development: Continuous learning, mentorship, and career growth opportunities.

  • Innovation & Technology: Work with cutting-edge CDM and clinical trial technologies.

  • Inclusive Work Culture: Thermo Fisher Scientific promotes diversity, inclusion, and equal opportunity for all employees.


About Thermo Fisher Scientific

Thermo Fisher Scientific is a global leader in serving science, with annual revenues exceeding $44 billion and over 90,000 employees worldwide. Our mission is to enable customers to make the world healthier, cleaner, and safer. We deliver innovative technologies, laboratory services, and pharmaceutical solutions through brands such as Thermo Scientific, Applied Biosystems, Invitrogen, Fisher Scientific, Unity Lab Services, and Patheon.

Equal Opportunity Employer – Thermo Fisher Scientific is committed to an inclusive and diverse workplace.