As a Global Medical Safety Lead you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.
What you will be doing:
- Provide strategic medical safety leadership and practical contributions for assigned product(s) in a cross-functional setting
- Perform safety signal management and benefit risk assessment activities as well as other regular and/or ad-hoc aggregate safety data reviews as needed for assigned product(s)
- Lead cross-functional teams to perform regular and/or ad-hoc review of existing and emerging aggregate safety data for assigned product(s)
- Contribute to the development of the overall safety governance structure and activities
- Provide safety strategies and deliver accurate, timely and high quality safety contributions for the preparation of relevant sections of regulatory submission documents globally (e.g. ISS, SCS, narratives) for assigned product(s)
- Prepare and/or review safety sections of clinical/regulatory documents (including study protocols, IBs, Clinical Study Reports, or ICFs)
- Provide medical safety support for the preparation of responses to regulatory authority inquiries. Assure that safety information is timely, complete, and accurate
- Lead the overall preparation of periodic safety reports (e.g. PSUR, DSUR); provide medical safety content and ensure consistency and quality of these documents
- Oversee the medical assessment of individual case safety reports (ICSR)
- Confirm criteria and content for expedited reporting and unblinding (e.g. SUSAR or urgent safety issues)
- Lead or actively contribute to the preparations and presentation of safety information to the Data Safety Monitoring Board (DSMB)
- Provide medical safety contributions at internal audits and regulatory inspections
- Support the development of and updates to GPS Standard Operating Procedures (SOPs) and other controlled documents (e.g. work instructions, forms, templates)
- Support adverse event reporting training and pharmacovigilance awareness activities cross functionally
- Support the preparation of pharmacovigilance agreements with clinical development or commercial business partners
- Participate in cross-functional teams and initiatives
- All other responsibilities as required
You Are:
- MD degree or equivalent required
- At least 7 years of relevant experience in the pharmaceutical/biotech industry with at least 5 years in pharmacovigilance/drug safety (global experience is a plus)
- At least 1 year of experience in clinical practice or in academic medicine
- Working knowledge of relevant pharmacovigilance regulatory requirements and guidance documents
- Demonstrated ability to perform medical assessments of safety data from multiple sources
- Experience with authoring complex documents and contributing to regulatory submissions
- Knowledge of adverse event reporting systems
- Experience in epidemiology, biostatistics, clinical development, or medical affairs is a plus
- Strong scientific and analytic skills
- Ability to complete multiple tasks concurrently and deliver results in a fast-paced environment
- Strong ability to lead, motivate, influence, and collaborate with multidisciplinary teams
- Excellent presentation skills with the ability to communicate complex issues clearly
- Relevant computer skills, including proficiency with Microsoft Office
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.
Our benefits examples include:
- Various annual leave entitlements
- A range of health insurance offerings to suit you and your family’s needs
- Competitive retirement planning offerings to maximise savings and plan with confidence for the years ahead
- Global Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised professionals who are there to support you and your family’s well-being
- Life assurance
- Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others
Visit our careers website to read more about the benefits of working at ICON: https://careers.iconplc.com/benefits
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 organization. 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 this form.
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