Director Of Pharmacovigilance & Safety

ICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organisations.

With our patients at the centre of all that we do, we help to accelerate the development of drugs and devices that save lives and improve quality of life.

Our people are our greatest strength, are at the core of our culture, and the driving force behind our success. ICON people have a mission to succeed and a passion that ensures what we do, we do well.

We are seeking a strong and dynamic strategic leader to oversee our PV and Safety function. The primary objective of the Director of Pharmacovigilance & Safety is to support and drive strategic and operational functions of the Pharmacovigilance & Safety business unit to meet its goals and project objectives.

The successful applicant will be responsible for the following.

• Leadership role for FSP PVG & Safety linked global team
• Reporting directly to VP and part of VPs leadership team covering Biometrics, Medical Writing, Regulatory and PVG & Safety functions
• Responsible for line management of PVG & Safety Management team providing guidance and support
• Responsible for providing direction and strategy for the FSP based PVG & Safety teams
• Key PVG & Safety leadership contact for FSP clients
• Responsible for key sales support for PVG & Safety team include input into RFPs, pricing and bid defence meeting support
• Provide strategic vision and leadership to define and implement global harmonized PV processes and technologies to support business objectives
• Stays abreast of PV and industry changes that may impact global PV operations. Interprets PV guidance as related to systems and makes plans to adapt company systems and processes as appropriate

• Minimum of 7 years of experience within Pharmacovigilance and Patient Safety
• Strong leadership skills 
• Experience working within a large global Clinical Research organization is highly preferred.
• Substantial experience working with external teams to support business development efforts is highly preferred
• Proven ability in implementing processes and procedures in support of improving PV technologies

Benefits of Working in ICON:Our success depends on the knowledge, capabilities and quality of our people. That’s why we are committed to developing our employees in a continuous learning culture – one where we challenge you with engaging work and where every experience adds to your professional development.At ICON, our focus is to provide you with a comprehensive and competitive total reward package that comprises, not only an excellent level of base pay, but also a wide range of variable pay and recognition programs. In addition, our best in class employee benefits, supportive policies and wellbeing initiatives are tailored to support you and your family at all stages of your career - both now, and into the future.ICON, including subsidiaries, is an equal opportunity and inclusive employer and is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know.