Support strategies and implement regulatory activities for assigned product and regulatory jurisdictions, with the intention of achieving successful registration and lifecycle management of unique and technologically complex products serving patients with rare diseases and unmet medical needs.
This individual will provide operational and strategic regulatory input to cross-functional teams responsible for driving programs in relevant regulatory jurisdictions.
The individual will also ensure effective communication and constructive working relationships with business partners and representatives of regulatory authorities.
Accountabilities Drive regulatory execution and implementation of regulatory strategies in the relevant regulatory jurisdiction, actively supporting relevant Regulatory Leads via the Regulatory Subteam (RSTs) to deliver on business objectives for assigned products/programs (e.g.
clinical trial applications, marketing authorization applications, orphan drug designation applications, paediatric submissions, etc.
).Contribute to the planning and conduct of regulatory authority meetings in relevant jurisdictions, providing input to submission strategy and other critical regulatory documents.
May represent Alexion as point contact with relevant Health Authorities and/or lead interactions with such authorities or other relevant external collaborators.Lead all aspects of operational activities and execution related to the Regulatory management in the relevant jurisdiction, in support of the Regulatory Lead, coordinating teams working on such deliverables.Support Regulatory Lead and contribute actively to internal Governance and advisory bodies, or other relevant internal activities, including on the development and management of select Regulatory processes and procedures, as well as inspection/audit support.Collaborate with Senior Management and Enterprise functions (e.g.
Clinical, Commercial, Medical Affairs, amongst others) to provide regional regulatory insight and broader drug development expertise.Keep up to date on the latest regulatory requirements and trends, and contribute to the shaping of the regulatory science environment!Essential Skills/Experience Bachelor's Degree, life science6+ years of Regulatory experience in the pharmaceutical industry.Strong knowledge of drug development and regulatory policy, excellent scientific and business judgment.Lead regulatory activities in at least one regulatory jurisdiction (e.g.
EU, US, China, Japan) for the global development of products through all stages of development including pre-approval and marketed assets.Manage complex issues and coordinate multiple projects simultaneously in a time-sensitive fashion.Build team relationships and collaborate in a global team environment at all levels of the organization, especially Senior Management.Strong written/verbal communication skills.Proven track record practicing sound judgment as it relates to risk assessmentKnowledge of new and emerging regulations and guidance'sUnderstanding of GxPs at relevant areas and solid understanding of where to seek and how to interpret regulatory information.Desirable Skills/Experience Postgraduate degrees relevant to the role (e.g.
MSc, PhD) a plusReady to make an impact?
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