Label Coordinator - Client Dedicated
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Thermo Fisher ScientificClinical supplies
This role can be based in Ireland, France, Croatia, UK or Bulgaria.Full-TimeJunior
Salary not disclosed
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Job Details
- Languages
- Intermediate English
- Experience
- Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to at least 2 years).
- Required Skills
- Microsoft OfficeAnalytical SkillsCustomer serviceAttention to detailTime Management
Requirements
- Have a high/secondary school diploma or equivalent and a relevant formal academic or vocational qualification.
- Have previous experience providing the knowledge, skills, and abilities to perform the job, comparable to at least 2 years.
- Understand clinical supply processes, including manufacturing, handling, importing, shipping, exporting, auditing, labeling, and packaging.
- Have intermediate English and good written and verbal interpersonal skills.
- Be proficient in Microsoft Office programs.
- Have strong planning and time-management skills and good analytical skills.
- Be able to work on issues of a diverse and confidential nature.
- Demonstrate customer service orientation and attention to detail aligned with high quality standards.
- Adapt to change and handle fast-paced situations.
- Be able to work independently with moderate direct supervision and as part of a team.
Responsibilities
- Support clinical supplies operations and administrative activities across the lifecycle of low- to moderate-complexity studies.
- Ensure activities comply with company good practices and client requirements.
- Participate in and support department project teams.
- Coordinate or serve as a liaison across functions when needed.
- Plan and coordinate label, patient card, and dosing card activities.
- Complete tasks according to PPD SOP requirements and client requirements.
- Coordinate the preparation and regulatory approval of information for clinical-trial labels, patient cards, and dosing cards.
- Review source documents and requests for quotes.
- Assist with developing and maintaining the Global Labelling Management tool.
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