Regulatory Submissions Manager - CRO
- Employer
- NonStop Consulting
- Location
- Sweden
- Salary
- Negotiable
- Closing date
- Oct 21, 2020
View more
- Sector
- Pharmaceutical, Clinical Manager/ Director
- Contract Type
- Employee
- Hours
- Full Time
- Organization Type
- Clinical Practice
- Jobseeker Type
- Professional
Job Details
My client is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries.
Their clinical operations activities are growing rapidly, and they are currently seeking a full-time, office-based Regulatory Submissions Manager to join their Clinical Operations team!
Qualifications
- At least 4 years of experience in clinical research, preferably with a CRO. Experience may include CRA or project management experience;
- Knowledge and experience of Clinical Trial Applications within Europe;
- Strong oral and written communication skills;
- Team-oriented approach and strong leadership skills; and
- Fluency in English and Swedish
If you or someone you know is open to a new opportunity - please do not hesitate to contact me for more information via k.aleksandraviciute@nonstop-recruitment.com
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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