FSP Project Manager (Clinical Trials)
Thermo Fisher Scientific Taipei, Taiwan
Biotechnology Research · 10,001+ employees
About the role
The Project Manager serves as the primary sponsor contact and is accountable for the overall delivery of clinical trial projects in terms of quality, time, and cost. They lead cross-functional teams, manage vendor relationships, and ensure compliance with regulatory requirements and internal policies.
What they look for
Requirements
Candidates must hold a bachelor's degree or equivalent and possess a minimum of 5 years of experience as a Clinical Trial Manager or Project Lead. Strong technical competency in clinical systems and advanced knowledge of clinical development guidelines are required.
Full description
Work Schedule
Standard (Mon-Fri)
Environmental Conditions
Office
Job Description
Join Us as a Project Manager - Make an Impact at the Forefront of Innovation The Project Manager serves as the Project Lead and primary sponsor contact and is accountable for the overall delivery of the project (quality, time, cost) on behalf of the organization. Additionally, the Project Manager establishes and communicates customer expectations to the project team and ensures that escalation pathways are adhered to internally and externally. The role involves leading the cross functional project team to meet or exceed deliverables.
What You'll Do:
- Serve as the primary contact between the sponsor and the organization at the project level, manage client communications. Manage / provide oversight to CROs, vendors, other stakeholders globally.
- Ensure escalation pathways adhered to internally and externally (Rules of Engagement – communication pathways).
- On projects where the scope requires, ensure clear delineation in responsibilities and communication pathways for secondary project leads (such as lead in a specific region, lead for a specific vendor(s) or subset of delivery).
- Accountable for the overall delivery of the cross-functional project (time, cost, quality).
- Ensure financial stewardship at a project level by demonstrating an intimate understanding of the contract, resource alignment to budget, management of Out of Scope activity, drive the Con Mod process/negotiations and team execution to timelines.
- Establish, communicate and manage customer expectations to achieve optimal delivery during the project
- Drive Risk Identification and Issue Resolution at project level (RBQM/RESOLVE).
- Ensure project team compliance with organization policies, SOPs, ICH- GCP, regulatory and project specific requirements.
Education & Experience Requirements:
- Bachelor's degree or equivalent and relevant formal academic / vocational qualification
- Minimum 5 years of experience as a Clinical Trial Manager or Project Lead.
- Prior experience in relevant therapeutic areas such as Internal Medicine, is preferred.
Knowledge, Skills, Abilities:
- Technical and systems competency, such as computer skills, to include effective use of systems and applications such as Microsoft Outlook, Word, Excel and PowerPoint, as well as organization systems (CTMS, Preclarus, Clarity)
- Ability to delegate and effectively prioritize own and workload of project team members in a frequently changing environment
- Effective oral and written communication and presentation skills
- Proactive, solutions oriented and adaptable to changing priorities and situations
- Advanced therapeutic area knowledge and clinical development guidelines and directives
- Strong understanding of the key principles of project management (time, quality, cost), including solid financial acumen
- Sound interpersonal and customer service skills, including the ability to lead, motivate and coordinate cross-functional project teams
- Good judgment and decision making skills and capable of applying critical and analytical strategic thinking skills to manage complex/ambiguous situations
- Ability to negotiate, persuade and influence others, including a cross cultural awareness.
Working Conditions and Environment:
- Work is performed in an office/ laboratory and/or a clinical environment.
- Exposure to biological fluids with potential exposure to infectious organisms.
- Exposure to electrical office equipment.
- Personal protective equipment required such as protective eyewear, garments and gloves.
Why Join Us?
When you join Thermo Fisher Scientific, you become part of a global team that values passion, innovation, and a commitment to scientific excellence. You’ll work in an environment where collaboration and development are part of the everyday experience—and where your contributions truly make a difference.
Apply today to help us deliver tomorrow’s breakthroughs.
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