Valeant Pharmaceuticals

Specialist, Global Pharmacovigilance & Risk Mgmt

US-NJ-Bridgewater
Job ID
9270
Category
R&D
Pos. Type
Full Time

Overview

Valeant Pharmaceuticals International, Inc. is a diverse and decentralized pharmaceutical company that is committed to focusing on our key stakeholders while delivering consistently high performance.  Our values provide the overall direction for our company, and provide us with the tools necessary to rise to any challenge by leveraging our collective hard work and effort along with our unwavering competitive spirit.  These values help us set goals based on our organization’s potential and what we hope it will become.

 

This position will assume responsibility for the preparation and maintenance and tracking of Safety Data Exchange Agreements (SDEAs).

Responsibilities

Responsible for SDEAs in all regions globally

-Prepares, maintains and reviews SDEAs and other Third Party Agreements
-Maintains Global SDEA Tracker
-Supports internal and external partners in SDEA-related matters
-Acts as contact point for business partners, other departments, third party provider(s) and authorities regarding SDEAs
-Direct reporting to Global SDEA Director
-Dotted line reporting to EU QPPV

 

Key relationships:

-Third Party provider(s)
-Business partners
-Regulatory Affairs
-Other Third Parties
-Quality Department
-Local/Regional Responsible Persons for Pharmacovigilance
-Medical Affairs
-Clinical Operations
-Business Development

Qualifications

-Pharmacist of Health Science Degree preferred.
-Experience in Pharmacovigilance required.
-Experience in SDEAs preparation desired.
-Strong organizational skills, detail-oriented, ability to adapt to a fast-paced and changing environment
-Proven written and oral communication skills in English
-Ability to work under pressure to meet tight deadlines

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