Trial Strategy Specialist III

Thermo Fisher Scientific

. Provide expert guidance in formulating and executing clinical trial strategies .

Posted 10/30/2026full-timeRemote • Alaska • United StatesMid-LevelSeniorWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in clinical trial strategy formulation and execution, with strong project management, proposal development, and operational strategy skills. Proven ability to collaborate effectively with stakeholders and manage complex opportunities in a high-pressure environment.

Highest-signal resume keywords

Clinical Project ManagementProposal DevelopmentOperational StrategyCustomer Relationship ManagementAnalytical Skills

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Clinical Trial StrategyProject ManagementProposal Development SkillsOperational Strategy ModelBudget Input and RevisionsKnowledge of SOPsGCPsFDA/ICH GuidelinesAttention to DetailMultitasking

Soft Skills

CollaborationInfluence and NegotiationOrganizational AgilityCommunication SkillsTime Management

Tools & Technologies

In-House SoftwareOff-the-Shelf Software

Industry Keywords

Sponsor/CRO Business PracticesClinical TrialsOperational PracticesCommercial Win StrategiesGlobal and Cultural Awareness

About the role

Key responsibilities & impact

Provide expert guidance in formulating and executing clinical trial strategies
Optimize trial processes
Collaborate with key stakeholders to ensure strategic alignment
Drive initiatives that enhance the success and efficiency of clinical trials
Collaborate with internal stakeholders on operational strategy for moderately complex opportunities
Provide budget input and revisions reflecting proposed operational strategy
Participate in developing and delivering the operational strategy model within proposed timelines
Conduct proposal reviews for alignment with operational and commercial win strategies
Collaborate with commercial and functional teams on formal proposal revisions
Assist the OSC role in larger, complex opportunities
Work independently with little guidance and plan work schedules to meet goals
Perform variable tasks under changing conditions, including multitasking under stress

Requirements

What you’ll need

Bachelor's degree or equivalent and relevant formal academic/vocational qualification
5+ years of previous relevant experience or equivalent combination of education, training, and experience
Thorough understanding of clinical project management, business organization, and functional areas
Solid customer relationship management skills and commercial acumen
Ability to work in a high-pressure, time-sensitive environment
Ability to multitask with attention to detail
Strong proposal development knowledge and skills
Project management and planning skills
Strong organizational agility and drive for results
Influence and negotiation skills
Ability to build effective collaborative peer and cross-functional relationships
Ability to work effectively in teams with global and cultural awareness
Analytical skills
Excellence in oral and written communications
Prioritization and time management proficiency
Thorough understanding of sponsor/CRO business practices
Knowledge of operational and financial practices, SOPs, GCPs, and FDA/ICH guidelines
Ability to access and use in-house and off-the-shelf computer software
Ability to communicate and understand spoken and written information
Regular and consistent attendance

Benefits

Comp & perks

Global team environment
Collaboration and development opportunities
Scientific excellence-focused workplace
Occasional domestic and international travel