Required Education: A Bachelor's degree in life sciences (pharmacy, biology, chemistry, pharmacology) or a related field.Preferred Education: An advanced degree in a relevant field is preferred, with certifications being an advantage.Required Experience: A minimum of 7 years in regulatory affairs, including significant pharmaceutical regulatory work. Proven drug development experience in the US and Canada, with at least 5 years in a strategic leadership capacity. Strong project management capabilities and experience in complex environments involving multiple stakeholders.Preferred Experience: Over 10 years of experience in the pharmaceutical industry, with a track record of developing and implementing successful global regulatory strategies.Skills: Exceptional communication and negotiation skills are essential to succeed in this role.
About the job
As the Director of Global Regulatory Strategy at AbbVie, you will play a pivotal role in shaping and executing comprehensive global regulatory strategies to secure and uphold market approvals for our innovative products within your designated therapeutic area. You will lead the Global Regulatory Product Team (GRPT) and continuously enhance your therapeutic area knowledge, ensuring that the strategic messaging and contents of global regulatory submissions are robust and aligned with industry standards. Additionally, you may lead the Labeling Regulatory Strategy Team (LRST) and act as the main regulatory liaison with the Asset Strategy Team (AST) and other supporting groups. Your proactive approach will be essential in identifying and mitigating regulatory risks while ensuring adherence to global regulations throughout all development phases and product lifecycles. Your expertise in drug development will be instrumental in driving acceleration strategies and managing essential regulatory projects and documentation.
About AbbVie Inc.
AbbVie is dedicated to discovering and providing innovative medicines that address significant health challenges today and prepare for the medical needs of tomorrow. Our mission is to create a profound impact on patients' lives across key therapeutic areas, including immunology, oncology, neuroscience, and eye care, alongside offerings in our Allergan Aesthetics portfolio. To learn more about AbbVie, please visit www.abbvie.com.
This job posting is no longer active and is not accepting applications.
Required Education: A Bachelor's degree in life sciences (pharmacy, biology, chemistry, pharmacology) or a related field.Preferred Education: An advanced degree in a relevant field is preferred, with certifications being an advantage.Required Experience: A minimum of 7 years in regulatory affairs, including significant pharmaceutical regulatory work. Proven drug development experience in the US and Canada, with at least 5 years in a strategic leadership capacity. Strong project management capabilities and experience in complex environments involving multiple stakeholders.Preferred Experience: Over 10 years of experience in the pharmaceutical industry, with a track record of developing and implementing successful global regulatory strategies.Skills: Exceptional communication and negotiation skills are essential to succeed in this role.
About the job
As the Director of Global Regulatory Strategy at AbbVie, you will play a pivotal role in shaping and executing comprehensive global regulatory strategies to secure and uphold market approvals for our innovative products within your designated therapeutic area. You will lead the Global Regulatory Product Team (GRPT) and continuously enhance your therapeutic area knowledge, ensuring that the strategic messaging and contents of global regulatory submissions are robust and aligned with industry standards. Additionally, you may lead the Labeling Regulatory Strategy Team (LRST) and act as the main regulatory liaison with the Asset Strategy Team (AST) and other supporting groups. Your proactive approach will be essential in identifying and mitigating regulatory risks while ensuring adherence to global regulations throughout all development phases and product lifecycles. Your expertise in drug development will be instrumental in driving acceleration strategies and managing essential regulatory projects and documentation.
About AbbVie Inc.
AbbVie is dedicated to discovering and providing innovative medicines that address significant health challenges today and prepare for the medical needs of tomorrow. Our mission is to create a profound impact on patients' lives across key therapeutic areas, including immunology, oncology, neuroscience, and eye care, alongside offerings in our Allergan Aesthetics portfolio. To learn more about AbbVie, please visit www.abbvie.com.