Thermo Fisher Scientific

Project Manager

Thermo Fisher Scientific Singapore, Singapore

Biotechnology Research · 10,001+ employees

Yesterday
project-manager Junior (0-2 yrs) Full-time Singapore
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About the role

Manage a portfolio of clinical trial projects, coordinating cross-functional activities from study setup through completion. Serve as the primary point of contact for clients while ensuring timely delivery of services according to quality standards.

What they look for

Clinical trials Project management Budget management GMP GxP Quality management systems Risk management Stakeholder management Documentation Communication Planning Analytical skills MS Office Cross-functional collaboration Process compliance

Requirements

Requires an advanced degree with no experience or a bachelor's degree with at least 2 years of experience in clinical trials or the pharmaceutical industry. Candidates must possess a strong understanding of GMP/GxP requirements and excellent organizational skills.

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:

  • Ensuring successful delivery of clinical trial projects and exceptional customer service.
  • Working autonomously or supporting senior project managers
  • Manage a portfolio of clinical trial projects, coordinating cross-functional activities from study setup through completion while serving as the primary point of contact for clients.
  • Manage end-to-end project coordination, including study specifications, timeline development, budget management, and documentation
  • Foster proactive communication and collaboration between internal departments and external clients
  • Ensure timely delivery of services and products according to client requirements and quality standards
  • Monitor project activities, identify and address risks, and implement solutions to keep projects on track
  • Develop strong client relationships while representing their needs throughout internal processes
  • Support continuous improvement initiatives and provide guidance to team members
  • Provide input into the writing and review of departmental SOPs and investigation reports.
  • Participate in client meetings, investigator meetings, teleconferences where appropriate

REQUIREMENTS:

  • Advanced Degree with no prior experience, or Bachelor's Degree plus 2 years of experience, preferably in clinical trials or pharmaceutical industry
  • Preferred Fields of Study: Life sciences, healthcare, business or Supply chain related field
  • Strong understanding of GMP/GxP requirements and quality management systems
  • Excellent organizational and planning abilities with demonstrated experience managing multiple complex projects
  • Advanced communication and presentation skills; able to effectively engage with clients and internal stakeholders
  • Proficient in project management tools and MS Office applications (Excel, PowerPoint, etc.)
  • Demonstrated financial acumen and budget management capabilities
  • Analytical approach with ability to identify and address risks
  • Detail-oriented with excellent documentation and process compliance skills
  • Self-directed while collaborating effectively in a matrix environment
  • English fluency required; additional languages beneficial
  • Client-focused with demonstrated ability to build and maintain professional relationships

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