Part-Time Senior Regulatory Affairs Cons
On behalf of my client, a regulatory affairs consultancy firm, I am recruiting for a Senior Regulatory Affairs Consultant. This is a permanent, part-time role. The successful candidate will manage key regulatory projects, provide regulatory advice to clients and prepare critical regulatory documentation. Applications are invited from candidates with the following background and experience: 1. Bachelors degree in pharmacy, a life science or a biomedical discipline. 2. In depth knowledge of the regulatory environment, guidelines and practice within EU. 3. Breadth of regulatory experience (4 years +) in drug development, MAA approval and post-licensing (e.g. experience in multiple products, multiple phases of development, multiple therapeutic areas. 4. Experience with EU regulatory procedures (Clinical Trial Submissions, CP, MRP, national. 5. Experience in the clinical development and/or biotech sectors are particularly desirable. 6. Excellent English, and written and oral communication skills. 7. Excellent project management, organisation and multi-tasking skills. 8. Superb attention to detail and accuracy. 9. Self-motivated, pro-active and capable of working independently, however can also work as part of a team. 10. Computer literacy. For a full Job Spec and to apply for this role please call Deirdre on +353 1 2784671 or e-mail email@example.com. Thornshaw Scientific Recruitment is a leading Irish provider of specialist Scientific Recruitment. Part of the CPL Group. www.thornshaw.com Tel: +353 1 2784671. This job originally appeared on RecruitIreland.com.
8 days ago