Pharmacovigilance Jobs
Regeneron Ireland DAC - Dublin
pharmacovigilance regulations, systems, and processes. Extensive knowledge of the adverse event lifecycle. Does this sound like you? Apply now to take your first step towards living the Regeneron Way 12000.0
from: irishjobs.ie (+1 source) - 5 days ago
Regeneron Ireland DAC - Dublin
Regeneron is seeking a Senior Manager for our QPPV operations department. The individual will play a key role in supporting the creation and maintenance of our Pharmacovigilance System Master File 12000.0
from: irishjobs.ie (+1 source) - 18 days ago
Regeneron Ireland DAC - Dublin
pharmacovigilance activities for both clinical trial and post-marketing environments Ability to work with a safety system database for purposes of medical case review and simple queries Able to be proactive and self 12000.0
from: jobs.ie (+1 source) - 9 days ago
CPL Recruitment - Dublin
contact for Medical Information Enquiries · Ensure compliance with all product safety, regulatory affairs and pharmacovigilance requirement · Ensure key Quality records are maintained in accordance Negotiable
from: cpljobs.com (+2 sources) - 11 days ago
Regeneron Ireland DAC - Dublin
pharmacovigilance regulations, systems, and processes. Extensive knowledge of the adverse event lifecycle. Does this sound like you? Apply now to take your first step towards living the Regeneron Way 12000.0
from: irishjobs.ie - 14 days ago
Regeneron Ireland DAC - Dublin
We are seeking an Associate Director in GPS Standards & Training to maintain the Pharmacovigilance (PV) Quality Management System. This role is important for ensuring compliance with regulatory PV 12000.0
from: jobs.ie (+1 source) - 15 days ago
Regeneron Ireland DAC - Dublin
role with expertise and/or transferable skills related to Good Clinical Practice (GCP), and/or Good Pharmacovigilance Practice (GVP). Does this sound like you? Apply now to take your first step towards 12000.0
from: irishjobs.ie (+1 source) - 15 days ago
Regeneron Ireland DAC - Dublin
governing pharmacovigilance activities for both clinical trial and post-marketing environments required. Function as a subject matter expert internal and external to GPS for assigned compounds with relevant 12000.0
from: jobs.ie (+1 source) - 15 days ago
CPL Recruitment - Dublin
, Regulatory, Project Management, Pharmacovigilance etc. Responsibilities: Establish appropriate system for clinical quality management and oversight a of investigational sites and vendors. Collaborate Negotiable
from: cpljobs.com - 17 days ago
TCP Group - Cork
. Administration of required IV/IM/SC injections and oral therapies to patients to the highest clinical and ethical standards Carry out all required activities including wound care and catheter care. Carry out
from: irishjobs.ie (+1 source) - 18 days ago