Thermo Fisher Scientific
10,000+ employees
Founded 1956
🧬 Biotechnology
💊 Pharmaceuticals
🔬 Science
Biotechnology • Pharmaceuticals • Science
Thermo Fisher Scientific is the world leader in serving science, with annual revenue of more than $40 billion. Their mission is to enable customers to make the world healthier, cleaner, and safer by supporting life sciences research, solving complex analytical challenges, increasing laboratory productivity, and improving patient health through diagnostics and the development of life-changing therapies. With a global team, they offer innovative technologies and pharmaceutical services through brands such as Thermo Scientific, Applied Biosystems, Invitrogen, Fisher Scientific, Unity Lab Services, Patheon, and PPD.
Label Coordinator
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Thermo Fisher Scientific
10,000+ employees
Founded 1956
🧬 Biotechnology
💊 Pharmaceuticals
🔬 Science
Biotechnology • Pharmaceuticals • Science
Thermo Fisher Scientific is the world leader in serving science, with annual revenue of more than $40 billion. Their mission is to enable customers to make the world healthier, cleaner, and safer by supporting life sciences research, solving complex analytical challenges, increasing laboratory productivity, and improving patient health through diagnostics and the development of life-changing therapies. With a global team, they offer innovative technologies and pharmaceutical services through brands such as Thermo Scientific, Applied Biosystems, Invitrogen, Fisher Scientific, Unity Lab Services, Patheon, and PPD.
📋 Description
• 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
• 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
• Competitive salary • Flexible work hours • Professional development budget • Home office setup allowance • Global team events
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