Country Approval Associate coordinating ethical and regulatory submissions for Thermo Fisher Scientific’s clinical - trial operations. Supporting site activation, study files, compliance packages, and country - level approvals.
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Thermo Fisher Scientific
Currently Hiring
About the company
About Thermo Fisher Scientific
Thermo Fisher Scientific Inc.
is the world leader in serving science, with annual revenue of approximately $40 billion.
Our Mission is to enable our customers to make the world healthier, cleaner and safer.
Whether our customers are accelerating life sciences research, solving complex analytical challenges, increasing productivity in their laboratories, improving patient health through diagnostics or the development and manufacture of life-changing therapies, we are here to support them.
Our global team delivers an unrivaled combination of innovative technologies, purchasing convenience and pharmaceutical services through our industry-leading brands, including Thermo Scientific, Applied Biosystems, Invitrogen, Fisher Scientific, Unity Lab Services, Patheon and PPD.
For more information, please visit www.thermofisher.com.
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7 jobs found
CMC regulatory leader guiding biologics submissions and lifecycle compliance for Thermo Fisher Scientific. Managing FDA and Health Canada dossiers, changes, and post - approval reporting.
Field Service Engineer maintaining Thermo Fisher laboratory instruments at customer laboratories across Canada. Installing, repairing and servicing scientific equipment while supporting customers and managing field - service documentation.
Medical Scientific Liaison advancing Thermo Fisher Scientific biomarker assays for maternal fetal medicine and prenatal screening. Building scientific partnerships and informing clinical strategy through customer education and medical insights.
Country Approval Specialist managing local regulatory submissions for pharmaceutical firms. Collaborating with global teams to support clinical trials across various countries.
Site Contract Specialist preparing, negotiating agreements for clinical trials with pharmaceutical companies. Ensuring compliance and efficient delivery of contracts within established processes.
Assistant CRA supporting clinical trials management for top pharmaceutical companies. Performing remote tasks for site management, ensuring compliance with protocols and regulations.