Average salary: €39,500 /yearly
More stats ...the Executive Director of Global Patient Safety (GPS) within our Quality and Compliance Centers of Excellence (CoE). As the GPS Pharmacovigilance Intelligence Leader, you'll become a central figure in ensuring patient safety by navigating the evolving landscape of international...
...information, please visit www.jazzpharmaceuticals.com and follow @JazzPharma on Twitter.
Brief Description:
~To lead Jazz’s Pharmacovigilance QA (GvP) function to assure regulatory compliance and data integrity in all Jazz activities related to Pharmacovigilance.
Essential...
£42.8k - £47.1k per annum
...landscape and review of medical device reports and product recalls.
* Collaborate with Device Development colleagues, Clinicians and Pharmacovigilance teams to analyse, evaluate, mitigate and control risks at the user interface in line with international standards and our...
...culture.
The Role
To provide administrative assistance & support on all matters associated with the operation of the Quality & Pharmacovigilance Departments, to include continuous updating & maintenance of the Company's Quality Management & Pharmacovigilance System....
...weekly/monthly documentation for departmental reviews
Report all adverse events and product complaints promptly in line with Pharmacovigilance procedures and current legislation.
Maintain customer confidentiality at all times.
Assist in ensuring that continuing quality...
...On behalf of my client, a global pharmaceutical company, we are working with them on a new role for a Pharmacovigilance and Clinical Quality Specialist. This is a full-time permanent role based in Dublin.
The Role & Responsibilities:
The main purpose of this cross...
...governance for GPS Safety Sciences deliverables including, but not limited to, Risk Management Plans, Signal Management, and the Pharmacovigilance System Master File.
Establish and refine key performance indicators to ensure overall quality and compliance with associated...
...well as product information and artwork management. Furthermore, you will collaborate with various internal stakeholders such as Pharmacovigilance, Quality Assurance, and Supply Chain, while also beginning to develop external relationships and networks across other companies...
...or in a Clinical Development role. Strong Expertise with 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 living the Regeneron Way! We have an...
...drug development and the ability to critically evaluate clinical study protocols, reports and publications.
•Good knowledge of pharmacovigilance and regulatory legislation and how it impacts the product portfolio.
•Strong presentation, negotiation and networking skills....
...Overview:
This position is to support the Global Patient Safety (GPS) department in business support of safety systems utilized for pharmacovigilance. This includes overseeing daily activities such as generating searches and output in support of departmental data requests,...
...Ability to apply and provide critical analysis of relevant FDA, EU and ICH guidelines, initiatives and regulations governing pharmacovigilance activities for both clinical trial and post-marketing environments required.
Function as a subject matter expert internal and...
...comprehensive global services that cover the entire product life cycle, including Clinical, post-submission Regulatory Affairs, Pharmacovigilance, Quality Assurance, Auditing, and cutting-edge automation solutions.
Responsibilities:
Responsible for the development and...