Reference Number: JO-1911-441393
Associate Director, Pharmacovigilance Agreements
Rate: Negotiable
Job Type: Permanent
Location: Dublin City Centre

Associate Director, Pharmacovigilance Agreements
Dublin, Ireland
Highly competitive salary + benefits!

Clinical Professionals have partnered with a growing biotech based in Dublin who require an experienced PV professional to join their team, due to an expanding pipeline within Rare Diseases and Neurology.

You will be working closely with the Qualified Person to maintain and develop PV processes, whilst having global outreach and leading the PV Agreements and Operations.

Responsibilities include:

– Management and overseeing operation related to PVA/ Service Level Agreement (SLA) and Safety Data Exchange Agreement (SDEA) and operations
– Oversight of quality, standards and training of parts of the pharmacovigilance division
– Input into the Quality Management System (QMS) ensuring compliance
– Revising and editing of Standard Operating Procedures (SOPs)
– Input into the Pharmacovigilance System Master File (PSMF)
– Liaising with stakeholders/ third parties
– Business development
– Adhering to global regulations
– Working cross functionally

– Pre and post market experience
– Knowledge of GVP and PV Compliance
– Building and maintaining relationships with vendors/ third parties
– Excellent communication and interpersonal skills
– 6+ years experience working in Pharmacovigilance
– Bachelors or Masters Life Science Degree or equivalent

If this role is of interest or for more information, please send your CV to nadine.hopson@clinicalprofessionals.co.uk or call (Nadine) on 01189594990.

Upload your CV and any other relevant file.
I would like to be contacted via SMS
I have read and agree to the Clinical Professionals Group Privacy Policy

Find our privacy policy here