FREE ACCESS
5,000–10,000 jobs/day
See all jobs on Scoutfield
Search thousands of fresh jobs every day.
Discover
- Fresh listings
- Fast filters
- No subscription required
Create a free account and start exploring right away.

Senior Project Manager – FSP
Thermo Fisher Scientific. Serve as the client-embedded Project Lead and primary sponsor contact .
Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in project management within clinical trials, including risk management, budget oversight, and cross-functional team leadership. Possesses advanced knowledge of regulatory compliance and clinical development guidelines, ensuring successful project delivery across multiple therapeutic areas.
Highest-signal resume keywords
Project ManagementClinical Trial ManagementCross-Functional Team LeadershipRegulatory ComplianceRisk Management
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills
Project Management PrinciplesClinical Development GuidelinesBudget OversightRisk IdentificationIssue ResolutionInformed Consent Form DevelopmentProtocol Amendment ImplementationTherapeutic Area KnowledgeFinancial AcumenAnalytical Skills
Soft Skills
Effective CommunicationNegotiation SkillsDecision-MakingCritical ThinkingAbility to Delegate
Tools & Technologies
Microsoft OutlookMicrosoft WordMicrosoft ExcelMicrosoft PowerPointMS ProjectCTMSTMFIWRSECOAECRF
Industry Keywords
Biotech ExperienceRare DiseaseAuto-ImmuneOncology Clinical TrialsICH-GCP Standards
About the role
Key responsibilities & impact- Serve as the client-embedded Project Lead and primary sponsor contact
- Own overall project delivery, including quality, time, and cost
- Establish and communicate customer expectations to the project team
- Lead cross-functional project teams and manage projects of increasing complexity
- Coordinate study teams, stakeholders, and CRO/vendors
- Deliver clinical studies end-to-end while aligning with sponsor processes, tools, and performance measures
- Oversee study timelines, budgets, CRO/vendor deliverables, out-of-scope activities, and contract modifications
- Lead risk management, mitigation, issue identification, escalation, and resolution
- Lead a complex rescue/transition study through transition planning, financial oversight, reconciliation, risk identification, issue resolution, and cross-functional coordination
- Provide ICF Project Management within Medical Writing
- Oversee global informed consent form development and protocol amendment implementation across multiple countries
- Manage sponsor review, country customization, translation readiness, and accelerated delivery timelines
- Maintain communication across study teams, sponsors, and stakeholders in compliance with regulatory requirements and ICH-GCP standards
Requirements
What you’ll need- Bachelor's degree or equivalent and relevant formal academic / vocational qualification
- 8+ years of comparable experience providing the knowledge, skills, and abilities to perform the job
- Biotech experience is a plus
- Rare disease, auto-immune, and/or oncology clinical trial background is a plus
- Technical and systems competency, including Microsoft Outlook, Word, Excel, PowerPoint, MS Project, CTMS, TMF, IWRS, eCOA, and eCRF databases
- 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: 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
- Ability to work independently with minimal supervision
- Ability to work in office/laboratory and/or clinical environments
- Ability to handle potential exposure to biological fluids, infectious organisms, and electrical office equipment
- Ability to use required personal protective equipment, including protective eyewear, garments, and gloves
Benefits
Comp & perks- Global team environment at Thermo Fisher Scientific
- Collaboration and development opportunities
- Opportunity to contribute to scientific excellence and breakthroughs