Posted on over 5 years ago by Larry O'Leary
Regulatory Affairs and Pharmacovigilance Manager, Clinical Development
Our client, a Pharmaceutical company based in Munster, now require a Regulatory Affairs and Pharmacovigilance Manager as a technical subject matter expert for product / clinical development projects and also to lead, develop and motivate their team to achieve targets in a dynamic fast paced environment.
The successful candidate will manage the regulatory team and lead assigned regulatory projects in early stage development including management of budget, time-lines and submission planning.
The ideal candidate will have proven experience in mentoring staff (including new hires) on pharmacovigilance, clinical processes and interactions - both internally and externally. Additionally line management experience in; scheduling, delegating and monitoring processes & workflows is required.
Please contact Larry on +353 1-2302400 / larry@rftgroup.ie
The RFT Group, BioPharmaceutical Division specialise exclusively in the recruitment of scientists, engineers and executives for the biotechnology, pharmaceutical and medical device sectors. www.rftgroup.ie