Thermo Fisher Scientific

Project Assistant II

Thermo Fisher Scientific
Posted 10/21/2026full-timeRemote • Kentucky • United StatesJuniorMid-LevelWebsite
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Core Competencies

Role fit
Core Competencies

Use this summary to align your resume positioning with the role.

Demonstrates proficiency in document management, version control, and quality assurance for clinical trial documentation. Exhibits strong organizational skills and attention to detail while maintaining compliance with regulatory standards.

Highest-signal resume keywords
Document ManagementVersion ControlMicrosoft Office ProficiencyAttention to DetailOrganizational Skills

About the role

Key responsibilities & impact
  • Provide administrative and document-focused project support for central laboratory clinical trial services
  • Prepare, format, revise, track, and quality-review study-related documentation using approved templates and departmental standards
  • Draft and distribute meeting minutes, action logs, trackers, and routine project correspondence
  • Maintain and update milestone logs, document inventories, status reports, and other study tracking tools
  • Perform document quality checks for completeness, formatting accuracy, version control, and SOP consistency
  • Support document routing, approval workflows, and electronic filing in approved document management systems
  • Organize and maintain electronic project files according to internal standards and regulatory expectations
  • Compile study documentation for internal review, sponsor requests, and audits
  • Enter and maintain accurate data in project management and tracking systems
  • Flag documentation discrepancies, missing information, and inconsistencies to the supervising project manager
  • Support preparation of standard reports and presentation materials
  • Perform additional administrative duties as assigned
  • Work under supervision with clearly defined responsibilities; do not lead studies or independently manage clients

Requirements

What you’ll need
  • Must be legally authorized to work in the United States without sponsorship
  • Must be able to pass a comprehensive background check, including a drug screening
  • High / Secondary school diploma or equivalent and relevant formal academic / vocational qualification
  • Previous experience providing the knowledge, skills, and abilities to perform the job, comparable to at least 2 years
  • Basic understanding of document management and version control practices
  • Strong attention to detail and ability to identify formatting errors, missing information, and inconsistencies
  • Proficiency in Microsoft Office applications (Word, Excel, Outlook, PowerPoint), including advanced formatting and document editing
  • Ability to follow structured templates and checklists accurately
  • Strong organizational skills and ability to manage multiple document assignments
  • Clear written communication skills appropriate for internal documentation
  • Ability to maintain accurate records and organized electronic files
  • Ability to learn and apply internal systems and document control platforms
  • Ability to follow detailed instructions and established processes
  • Demonstrated discretion in handling confidential clinical and business information
  • Ability to work effectively in a structured, process-driven environment under supervision
  • Ability to perform occasional drives to site locations and potential occasional travel
  • Ability to use a variety of computer software developed in-house and off-the-shelf
  • Regular and consistent attendance
  • Ability to multi-task and perform under stress

Benefits

Comp & perks
  • Fully remote work arrangement
  • Potential occasional travel required
  • Accessibility service/accommodations for job seekers with disabilities
  • Opportunities to collaborate with industry-leading experts
  • Growth within an environment valuing innovation, accountability, and continuous development

ATS Keywords

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Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills
Document Quality ChecksData EntryDocument FormattingSOP ConsistencyProject TrackingMeeting Minutes DraftingAction Logs MaintenanceElectronic FilingReport PreparationTemplate Usage
Soft Skills
Clear Written CommunicationAbility to Multi-taskDiscretion in Handling Confidential InformationAbility to Follow Detailed InstructionsAbility to Work Under Supervision
Tools & Technologies
Document Management SystemsProject Management SystemsMicrosoft WordMicrosoft ExcelMicrosoft OutlookMicrosoft PowerPoint
Industry Keywords
Clinical Trial ServicesRegulatory ComplianceInternal ReviewAudit PreparationStructured Process