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Thermo Fisher Scientific

Label Coordinator

Thermo Fisher Scientific

Label Coordinator providing administrative support in clinical supplies lifecycle activities within a global team. Ensuring compliance and collaborating across various project teams.

Posted 7/15/2026full-timeRemote • 🇮🇪 IrelandJuniorMid-LevelWebsite

Core Competencies

Role fit
Core Competencies

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

Demonstrates proficiency in Clinical Supply processes and regulatory compliance while effectively coordinating clinical supplies operations and administrative activities. Strong planning, analytical, and customer service skills are essential for managing diverse tasks and ensuring attention to detail.

Highest-signal resume keywords
Clinical Supply Process UnderstandingPlanning And Time ManagementAnalytical SkillsMicrosoft Office ProficiencyInterpersonal Communication

ATS Keywords

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Applicant Tracking System Keywords

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

Soft Skills
Customer Service OrientationAttention To Detail
Tools & Technologies
Global Labelling Management Tool
Industry Keywords
Clinical TrialsRegulatory ApprovalGood PracticesSOP Requirements

About the role

Key responsibilities & impact
  • Provides support to clinical supplies operations and administrative activities in all areas of clinical supplies lifecycle of low to moderate complexity studies
  • Ensures all activities are driven in compliance with company good practices and client requirements
  • Participates in and supports department project teams
  • May coordinate or serve as a liaison cross-functionally
  • Plans and coordinates label, patient card, and dosing card activities
  • Ensures tasks are completed as needed according to PPD SOP requirements and/or client requirements
  • Coordinates the preparation and regulatory approval of information to be included on labels, patient cards, and dosing cards in clinical trials
  • Reviews source documents and requests for quotes
  • Assists with the development and maintenance of the Global Labelling Management tool

Requirements

What you’ll need
  • High / Secondary school diploma or equivalent
  • Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to at least 2 years)
  • Intermediate English and good interpersonal skills both written and verbal
  • Proven understanding of the Clinical Supply process
  • Strong planning and time management skills
  • Good analytical skills and ability to work on issues of a diverse and confidential nature
  • Proficient in Microsoft Office programs
  • Strong customer service orientation and attention to detail

Benefits

Comp & perks
  • Competitive salary
  • Flexible work hours
  • Professional development budget
  • Home office setup allowance
  • Global team events