Regulatory Affairs Manager US - innovative oncology treatments
- Employer
- NonStop Consulting
- Location
- Boston
- Salary
- Negotiable
- Closing date
- Feb 25, 2021
View more
- Sector
- Science, Life Sciences, Cell and Molecular Biology
- Contract Type
- Employee
- Hours
- Full Time
- Organization Type
- Corporate
Job Details
Are you looking for an opportunity that will allow you to make a difference in the development of lifesaving technologies? Look no further!
My client is an innovative biotech company leading in the development of novel radiotherapy techniques for oncology treatments. This exciting and fast growing company is currently looking for an experienced Senior US Regulatory professional who will play a key role in the development and execution of regulatory strategies
The position will be responsible for managing FDA submissions, leading interactions with regulatory bodies and representing the regulatory department in project development teams.
Requirements:
- 5+ Years of experience in regulatory affairs for the pharmaceutical/biotech industries
- Experience with FDA submissions and interactions
- Prior oncology experience is preferred
Company
Our Consultants are trained to deliver an exceptional standard of recruitment services to clients across the life sciences, chemical, care, educations, technical, digital and finance industries.
Our clients – and bottom line profits - tell us that we do a great many things very well. Complacency, however, is the last word you would associate with us. We work incredibly hard to deliver better and better results, based on stronger and stronger service delivery. Which is why we believe the best is yet to come – for us, our clients and for the people who have what it takes to join us on the journey.
The result? We’re expanding (in the UK and across Europe and even to Boston, US) and continue to post impressive performances in all our niche sectors.
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