Senior Project Manager, FSP

• Serve as the primary contact between the sponsor and Thermo Fisher Scientific at the project level
• Act as Project Lead and primary sponsor contact, accountable for overall project quality, time, and cost delivery
• Establish and communicate customer expectations to the project team
• Ensure internal and external escalation pathways are followed
• Define responsibilities and communication pathways for secondary project leads when required
• Lead cross-functional projects of increasing complexity, including multi-service, multi-region/country, therapeutic, and financial complexity
• Manage project financial stewardship, including contract understanding, resource alignment, out-of-scope activity, change management negotiations, budgets, forecasts, and timelines
• Identify project risks and resolve issues at project level using RBQM/RESOLVE
• Ensure project team compliance with policies, SOPs, ICH-GCP, regulatory, and project-specific requirements
• Mentor team members
• Develop or contribute to process improvement initiatives

• Bachelor’s degree or equivalent, supported by relevant academic or vocational qualifications
• 8+ years of comparable experience
• Master’s degree and background in biomedical or life sciences preferred
• Technical and systems competency, including Microsoft Outlook, Word, Excel, PowerPoint, CTMS, Preclarus, and Clarity
• Ability to delegate and prioritize workload and resources in a changing environment
• Effective oral, written communication, and presentation skills
• In-depth therapeutic area knowledge and clinical development guidelines and directives
• Advanced knowledge of cross-functional project management principles covering time, quality, and cost
• Ability to lead, motivate, and coordinate cross-functional project teams
• Strong customer service, negotiation, financial acumen, judgment, decision-making, critical thinking, and analytical skills
• Cross-cultural awareness
• Ability to work independently with minimal supervision
• Compliance with organization policies, SOPs, ICH-GCP, regulatory, and project-specific requirements

• Fully remote work mode
• Standard Monday–Friday work schedule
• Collaboration and development opportunities
• Opportunity to contribute to scientific innovation and breakthroughs