Regulatory Submissions Manager - Clinical Trials
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!
- 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
If you or someone you know is open to a new opportunity - please do not hesitate to contact me for more information via firstname.lastname@example.org