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Thermo Fisher Scientific

Safety Reporting Coordinator

Thermo Fisher Scientific

. Provide administrative safety support to the Pharmacovigilance department .

Posted 10/8/2026full-timeRemote • MexicoJuniorMid-LevelWebsite

Core Competencies

Role fit
Core Competencies

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

Demonstrates proficiency in administrative support within Pharmacovigilance, including safety reporting processes, document management, and effective communication. Capable of training staff and maintaining organizational systems while ensuring compliance with SOPs and WPDs.

Highest-signal resume keywords
Pharmacovigilance SupportSafety Reporting ProcessesMicrosoft Office ProficiencyAttention to DetailOrganizational Skills

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
Safety ReportingDocument ManagementQuality ChecksClinical Trial Management SystemFiling and ArchivingReport ReconciliationMetrics TrackingBarcode Safety ReportsAudit ReadinessProblem-Solving
Soft Skills
Excellent Communication SkillsTime ManagementTeam CollaborationStress ManagementOrganizational Skills
Tools & Technologies
Microsoft WordMicrosoft ExcelMicrosoft PowerPointMicrosoft Access
Certifications & Qualifications
High School DiplomaVocational Qualification
Industry Keywords
PharmacovigilanceSOPsWPDsClinical TrialsSafety Reports

About the role

Key responsibilities & impact
  • Provide administrative safety support to the Pharmacovigilance department
  • Submit safety reports to applicable parties and complete scanning, indexing, filing, tracking, quality checks, and archiving in accordance with SOPs and WPDs
  • Resolve simple problems with submission packs
  • Liaise with relevant teams on administrative safety reporting tasks, audit readiness, meeting organization, minute taking, filing, photocopying, work distribution, report reconciliation, metrics, and system updates
  • Extract and collate reporting information via the Clinical Trial Management System
  • Maintain and update contact lists in organizational systems
  • Support department and Pharmacovigilance initiatives
  • Train Pharmacovigilance staff on safety reporting processes and associated systems
  • Provide filing support, barcode safety reports, identify inaccuracies, and maintain file-room cleanliness and organization
  • Assist with completed safety report file reviews, audit notifications, file return notifications, and on-site audits
  • Coordinate study files and inventories for clients, including distribution through external postal services

Requirements

What you’ll need
  • High / Secondary school diploma or equivalent and relevant formal academic / vocational qualification
  • Technical positions may require a certificate
  • Previous experience comparable to at least 2 years
  • Equivalency through a combination of appropriate education, training and/or directly related experience may be considered
  • Proficiency in Microsoft Office Programs (Word, Excel, PowerPoint, Access)
  • Solid knowledge of procedural documents
  • Excellent written and verbal communication skills
  • Excellent organization and time management skills
  • Proven ability to handle multiple tasks simultaneously and deal effectively with stress
  • Strong attention to detail and accuracy
  • Strong problem-solving skills
  • Ability to work effectively in a team and support assigned lead and line manager
  • Occasional travel or drives to site locations may be required

Benefits

Comp & perks
  • Meaningful work with a positive global impact
  • Resources to achieve individual career goals
  • Collaboration and professional development opportunities
  • Fully remote work arrangement
  • Standard Monday–Friday work schedule