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Regulatory Affairs and Pharmacovigilance Manager, Clinical Development

Posted on 8 months ago by Larry O'Leary

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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
 

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