Jobs at Parexel
Are you ready to make your mark in the healthcare industry using your ingenuity and technical expertise? At Parexel, there's no limit to what you can accomplish. We work with the top 50 global pharmaceutical companies, the top global biotech companies, and hundreds of small and emerging companies. We've supported the development of some of the most important treatments of our time, including nearly all of the 50 top selling drugs currently on the market. Join us and you'll make a profound difference in millions of lives. With a role in our Information Technology group, you'll work with cutting-edge technology on internal and client-facing projects. Collaborating with people from all over the world and touching everything from enterprise systems and clinical applications to infrastructure and networking, you'll keep our data safe and confidential. You'll have the chance to develop your skills and pursue advancement opportunities that include managerial and technical tracks. If you have stellar coding and design experience and a passion to learn more about healthcare, Parexel invites you to discover our rewarding opportunities in Enterprise Architecture, Software Development, Project Management and Business Analysis, and more. In a global clinical trial environment, business-focused applications, connectivity, and data security are critical to a trial's outcome. Find out how you can be an invaluable part of our success story.
Local Qualified Person for Pharmacovigilance (QPPV) Freelancer - TALENT POOL
Job ID R0000020682 , RemoteParexel is in the business of improving the world’s health. We do this by providing a suite of biopharmaceutical services that help clients across the globe transform scientific discoveries into new treatments. From clinical trials to regulatory, consulting, and market access, our therapeutic, technical, and functional ability is underpinned by a deep conviction in what we do. We believe in our values; Patients First, Quality, Respect, Empowerment & Accountability.
The Pharmacovigilance team are looking to build a network of Local Qualified Person for Pharmacovigilance (QPPV) FREELANCERS for future projects.
The role can be based remotely in select EMEA locations and Australia.
Requirements
Expert knowledge of local PV legislation in territory(ies) where assigned as the Local QPPV
Minimum of at least 7 years' demonstrated experience in managing or implementing PV systems, including quality assurance experience
Documented experience in all aspects of PV in order to fulfill the responsibilities of the Local QPPV.
Extensive knowledge of global pharmacovigilance regulations and GVP and GCP guidelines
Experience in pharmacovigilance safety risk management including clinical trials, post-market pharmacovigilance, safety case processing, safety reporting, and safety systems
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