Role at a glance
- Job function
-
Product, Strategy & Operations Program & Project Management
- Salary
- Not Disclosed
- Location
- Singapore
- Work arrangement
- On-site
- Employment
- Full-time
- Experience
- Advanced Degree with no prior experience, or Bachelor's Degree plus 2 years of experience
- Education
- Bachelor's Degree
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Role Summary
This role manages clinical trial projects from study setup through completion and serves as the primary point of contact for clients. The position coordinates cross-functional delivery, maintains client relationships, and supports quality and continuous improvement activities.
What You'll Do
- Manage a portfolio of clinical trial projects and coordinate cross-functional activities
- Manage study specifications, timelines, budgets, and documentation
- Foster communication and collaboration between internal departments and external clients
- Monitor project activities, identify risks, and implement solutions
- Participate in client meetings, investigator meetings, and teleconferences
- Provide input into departmental SOPs and investigation reports
Generated from the employer's posting. Verify important details before applying.
View full postingQualifications
Strong understanding of GMP/GxP requirements and quality management systems; excellent organizational and planning abilities; advanced communication and presentation skills; proficiency in project management tools and MS Office applications; financial acumen and budget management capabilities; analytical approach to identify and address risks; documentation and process compliance skills; English fluency; ability to build and maintain professional relationships.
Required
- 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
- 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
Preferred
- Life sciences, healthcare, business or Supply chain related field
- preferably in clinical trials or pharmaceutical industry
- additional languages beneficial
Original job description
Content provided by the employer
Original job description
Content provided by the employer
Work Schedule
Standard (Mon-Fri)Environmental Conditions
OfficeJob 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
About the company
Thermo Fisher Scientific
Large Enterprise
Thermo Fisher Scientific is a global leader in serving science, providing a wide range of analytical instruments, reagents, and software solutions for healthcare, pharmaceuticals, and life sciences research. With a commitment to innovation and quality, the company enables customers to make significant advancements in scientific discovery and healthcare diagnostics. Thermo Fisher operates in more than 50 countries and employs over 80,000 people, fostering a collaborative environment aimed at enhancing global health and safety. Through its broad portfolio of brands and technologies, the company plays a vital role in accelerating life-changing research and improving patient outcomes worldwide.