Analytical Instruments • Laboratory Supply Chain Programs and eCommerce • Laboratory Equipment • Lab Services • Specialty Diagnostics
10,000+
October 8
Analytical Instruments • Laboratory Supply Chain Programs and eCommerce • Laboratory Equipment • Lab Services • Specialty Diagnostics
10,000+
• Join a global team in Regulatory Affairs at Thermo Fisher Scientific. • Lead discussions and coordinate regulatory strategies for clinical trials. • Provide regulatory intelligence and guidance to clients. • Act as a liaison with internal and external clients. • Arrange, lead, and report on regulatory meetings. • Prepare global regulatory submissions and assess clinical trial documents.
• Bachelor's degree or advanced degree preferred, or equivalent academic qualification. • Previous experience providing the knowledge, skills, and abilities for the job. • Knowledge of global clinical trials landscape. • Excellent command of English and local language (if applicable). • Exceptional interpersonal and communication skills. • Advanced computer skills including Microsoft Office Suite. • Strong organizational and time management skills. • Capability to work independently and exercise judgment. • Expert knowledge of ICH and other global regulatory guidelines.
• Award-winning learning and development programme ensuring professional growth. • Extensive benefits package centered on health and well-being. • Flexible working culture that values work-life balance.
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