Senior Pharmacovigilance Associate

As a Pharmacovigilance Associate, you will be joining the world's largest & most comprehensive clinical research organisation, powered by healthcare intelligence.

You will be expected to perform case processing for serious adverse events, serious and non-serious adverse drug reactions, and other medically-related project information such as adverse events of special interest and clinical endpoints. Provide input and review relevant safety tracking systems for accuracy and quality, assist with maintaining project files, and serve as a resource for investigational sites and ICON personnel on safety-related issues.

You will be partnering with one of our global pharmaceutical clients; a science-based company with one of the most exciting product pipelines in the industry. This global pharmaceutical client develops breakthrough innovative medicines to improve and extend the opportunity to build your career in a rewarding customer-focused environment that supports creativity, collaboration, and performance.

What you will be doing:

• Review and process safety events (pre-marketing, post-marketing, device and drug) and/or other medically related information per assigned tasks and project specific procedures.
• Perform review of abstracts and full articles to identify safety information from literature sources for both pre and post-marketed products.
• Respond and process medical information inquiries including inquiries related to adverse events and product complaints for Clients' product(s), as per their agreement with ICON.
• Complete adverse event follow-up in writing and/or by phone based on requirements for each Client.
• Provide input and review relevant safety tracking systems for accuracy and quality and assist with maintaining project files.
• Perform safety review of clinical and diagnostic data as part of case processing.
• Assist with generation of project specific procedures.
• Act as lead Drug Safety Associate for local or regional projects.
• Liaise with investigational site, reporter, and/or Sponsor as necessary regarding safety issues.
• Liaise with ICON Medical Monitor, project manager, and other departments, as appropriate.
• Assist with identifying out of scope activities in conjunction with the PV Project lead (as applicable).
• Attend project team and Sponsor meetings (including Investigator meetings) and teleconferences as required.

You are:

• Bachelor's degree in the health field, preferably in Pharmacy.
• Experience with case processing in Pharmacovigilance with human health drugs.
• Advanced English level.

What ICON can offer you:

Our success depends on the quality of our people. That's why we've made it a priority to build a diverse culture that rewards high performance and nurtures talent. In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work-life balance opportunities for you and your family.

At ICON, diversity, inclusion & belonging are fundamental to our culture and values. Our rich diversity makes us more innovative which helps us better serve our people, patients, customers, and our communities. We're proud of our diverse workforce and the work we've done to become a more inclusive organisation. We're dedicated to providing an inclusive and accessible environment for all candidates. ICON 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 through the form below.

Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless - there's every chance you're exactly what we're looking for here at ICON whether it is for this or other roles.