Project Assistant II

Posted 1ds ago

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Job Description

Project Assistant supporting document control and administrative tasks for Thermo Fisher Scientific’s global clinical laboratory trials. Maintaining audit-ready records, trackers, and study documentation.

Responsibilities:

  • 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:

  • 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:

  • 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