Similar posts
Senior Regulatory Executive
- Contract
- Senior/Director & VP, Officer /Associate
- United States
This vacancy has now expired. Please see similar roles below...
Proclinical is currently recruiting for a Senior Regulatory Executive for a pharmaceutical company located in Rockville, MD.
Job Responsibilities:
- Prepare high quality, detailed regulatory documents using varied information sources.
- Liaise closely with other personnel to ensure accuracy of such records.
- Work to agreed deadlines and maintain records reflecting project status.
- Highlight potential delaying factors promptly to line management and sharing knowledge of regulatory documentation and procedures with others to assist in problem solving.
Skills and Requirements:
- Bachelor's degree required; Advanced degree preferred
- 5+ years of experience working within pharmaceutical Regulatory Affairs
- Strong technical writing skills
To Apply:
Please click on the Apply button. Please include a short note outlining why you are interested in the role and why you think you are suitable.
In case you have difficulty in applying or if you have any questions, please call Sarah Beshara at (+1) 267-477-3355 or upload your resume on our website - www.proclinical.com.
A full job description is available on request.
Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.
Proclinical Staffing is an equal opportunity employer.
#LI-SB4
#RegulatoryAffairs
Related jobs
Highly Competitive Salary
Maidenhead, England
Proclinical is seeking a Global Regulatory Strategist who will play a key role in our regulatory affairs team. This is a remote contract position.
Highly Competitive
Hampshire, England
Proclinical are seeking a dedicated professional for a Regulatory Associate position
Highly Competitive Salary
Boston, USA
Proclinical is seeking a Senior Regulatory Affairs Associate or a Regulatory Affairs Consultant with a strong background in CMC post-approval.