Start-up Manager

Thermo Fisher Scientific

. Collaborate with team members in a matrix environment to deliver site activation for assigned projects .

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

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in project management and site activation within clinical research, ensuring adherence to timelines, quality standards, and budget controls. Possesses strong cross-functional collaboration skills and the ability to identify and mitigate risks effectively.

Highest-signal resume keywords

Project ManagementSite ActivationClinical Research KnowledgeCross-Functional Team CoordinationRisk Identification and Mitigation

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Project Implementation PlanningFinancial ManagementContractual ManagementMetrics AnalysisFeasibility AssessmentQuality ControlClinical Development GuidelinesMedical TerminologyStudy Phases KnowledgeContingency Planning

Soft Skills

Organizational SkillsAttention to DetailMultitaskingCross-Cultural AwarenessCommunication Skills

Tools & Technologies

PPD ToolsComputer Software

Certifications & Qualifications

Bachelor's Degree or Equivalent

Industry Keywords

Clinical ResearchSite ContractsProject Resources ManagementCross-Functional CollaborationTherapeutic Areas

About the role

Key responsibilities & impact

Collaborate with team members in a matrix environment to deliver site activation for assigned projects
Oversee site activation according to timelines and quality standards
Coordinate information flow between PPD teams, clients, and functional departments
Develop project implementation plans and guidelines using PPD tools
Monitor and analyze project status and provide metrics to upper management
Identify risks and develop contingency plans
Manage financial and contractual aspects of studies related to site activation
Establish controls to align project resources and expenses with budgets
Administer technical and operational aspects of site activation, including feasibility, site contracts, and country-team coordination
Manage assigned scope of work against timelines, costs, and quality
Identify and evaluate issues affecting successful site activation and implement solutions
Develop customer relationships aligned with assigned projects
Travel to domestic and international site locations up to 20% of the time

Requirements

What you’ll need

Bachelor's degree or equivalent and relevant formal academic / vocational qualification
Previous experience comparable to 5+ years
Equivalency through a combination of appropriate education, training and/or directly related experience may be considered
Ability to work efficiently with cross-functional teams
Knowledge of cross-functional project management principles
Organizational and multitasking skills
Attention to detail
Ability to identify and remedy risks related to contractual deliverables
Cross-cultural awareness and adaptability
Comprehensive understanding of clinical research/development, medical and therapeutic areas, study phases, and medical terminology
Ability to lead, liaise, and coordinate cross-functional project teams
Comprehensive knowledge of clinical development guidelines and Directives
Ability to use in-house and off-the-shelf computer software
Ability to communicate and understand spoken and written information
Ability to perform under stress and multitask
Regular and consistent attendance

Benefits

Comp & perks

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