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Thermo Fisher Scientific

Clinical Trials - Client Services Project Manager I

Thermo Fisher Scientific São Paulo, São Paulo, Brazil

Biotechnology Research · 10,001+ employees

Yesterday
project-manager Mid (2-5 yrs) Full-time Brazil
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About the role

Manage clinical trial project set-up, coordinate supply chain activities, and ensure consistent service delivery. Collaborate with internal teams to maintain quality standards and meet project timelines.

What they look for

Project management Clinical trials Supply chain management GMP GxP Quality management systems Microsoft Office Excel Microsoft Project Analytical skills Problem-solving Communication skills Documentation management Stakeholder management Data analysis Cross-functional coordination

Requirements

Requires a bachelor's degree in a relevant field such as healthcare, life sciences, or supply chain management. Candidates must have a strong understanding of GMP/GxP principles and demonstrated project management experience.

Full description

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Office

Job Description

As part of the Thermo Fisher Scientific team, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier, cleaner and safer. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the world’s toughest challenges, like protecting the environment, making sure our food is safe or helping find cures for cancer.

DESCRIPTION: Join our team at Thermo Fisher Scientific and contribute to advancing clinical research. As a Client Services Project Manager I, you'll support clinical trials by managing project set-up, coordinating supply chain activities, and ensuring consistent delivery of services. Work closely with internal teams to support study success while maintaining the highest quality standards. You'll handle project planning, documentation management, and cross-functional coordination to meet timelines and client expectations.

REQUIREMENTS:

  • Bachelor's degree required, preferably in clinical trials or pharmaceutical industry
  • Preferred Fields of Study: healthcare, supply chain management, life sciences, or related field
  • Strong understanding of GMP/GxP principles and quality management systems
  • Demonstrated project management skills with ability to handle multiple projects simultaneously
  • Advanced proficiency in Microsoft Office, especially Excel and Project
  • Strong analytical and problem-solving capabilities
  • Effective written and verbal communication skills
  • Detail-oriented with excellent organizational and documentation abilities
  • Demonstrated ability to work independently and as part of cross-functional teams
  • Intermediate / Fluent English required, additional languages beneficial
  • Experience coordinating with teams and managing stakeholder relationships
  • Ability to analyze data and generate clear, accurate reports
  • Focus on quality service and continuous improvement
  • Adaptable to changing priorities while maintaining attention to detail

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