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Regulatory Affairs Specialist. Imaging Endpoints (IE) is an Imaging Clinical Research Organization (iCRO) that also provides comprehensive CRO and Site Management Organization (SMO) services. We are based in Scottsdale, Arizona, with an office in Waltham, Massachusetts. We are an affiliate of HonorHealth, one of the largest healthcare systems.

Job Title. Senior Regulatory Affairs Specialist. Requisition. JR000012695 Senior Regulatory Affairs Specialist (Open) Location. St. Louis, MO (Pharma) - USA032.

Regulatory Affairs Specialist (Remote) BAXTER 3.8. Remote in Skaneateles Falls, NY 1 location. Estimated 64.6K - 81.8K a year. Full-time. 2 years of experience in regulatory preferred. Compile, edit, and proofread regulatory documents for submission under supervision and track status and progress.

The minimum requirement for aspiring regulatory affairs specialists is a bachelor&x27;s degree. Regulatory affairs workers come from a wide variety of fields. Many of them possess undergraduate degrees in engineering, clinical sciences, or public health. However, others come from business and economics degree programs or even a liberal arts background.

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An innovative start-up digital health company backed by grants are looking for a RA Specialist &183; Assist in the review of current global legislation for changes to legislation affecting technical file information and submissions andor status requirements. 183; Support the RA Manager to monitor and identify any changes to relevant medical device.

Entry requirements Individual employers will set their own selection criteria but entrants will typically already have a degree in science, engineering or law. English and Maths Apprentices without Level 2 English and Mathematics need to achieve this level prior to taking the end-point assessment.

Key Requirements - Minimum 3 years of experience or in Regulatory Affairs, public policy or Trade Associate Related field - Regulatory Affairs fundamentals - B.S or equivalent in a technical area, such as food science or veterinary medicine or food safety or chemistry, nutrition or other biological science. Whats on Offer - Regulatory Affairs.

As a Regulatory Specialist at Rimsys, you will collaborate with internal and external stakeholders by defining and clarifying regulatory requirementsworkflows and demonstrating coverage within.

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Regulatory Affairs Specialist. PREVOR. Other jobs like this. full time. Published on www.neuvoo.com 05 Nov 2022. Field medical device chemical risk management first aid solutions after industrial accidents. Main Office Mumbai. Skills Regulatory Affairs CMC, experience in regulatory submissions; medical devices. Education Master in Pharmacy.

The Regulatory Affairs Specialist role is a key contributor to the companys regulatory group focused on labeling support for AVITA Medicals regenerative products. This individual.

The RA Support Specialist will be responsible for supporting the management of the copy approval process for advertising and promotional collateral across the APAC region. This will be accomplished by partnering with our internal and external stakeholders and working within our internal digital asset management tool to traffic & monitor.

Ability to work independently and as a member of a team Capable of managing multiple projects simultaneously Experience 2-3 years of professional work experience in Regulatory Affairs Experience in medical device labeling, advertising, and promotional material review EducationTraining Degree in engineering or physicalbiological sciences.