As a Senior Regulatory Affairs Director you’ll play a pivotal role in channeling our scientific capabilities to make a positive impact on changing patients’ lives. R&D Oncology drives late-stage development of our innovative pipeline, transforming exciting science into valued new medicines and ensuring patients around the world can access them. 

What you'll do: 

As the Senior Regulatory Affairs Director you will be accountable for leading the development and implementation of the global regulatory strategy for a product/group of products of increasing complexity. You will ensure that the strategy is designed to deliver rapid approval with advantageous labeling in keeping with the properties of the product(s) and the needs identified by the business, markets and patients. You will show strategic leadership skills, and a deep understanding of global regulatory science and overall drug/biologic development processes and strategies for high profile, complex or novel development programs. 

You will lead the planning and construction of the global dossier and core prescribing information.  You will conduct regulatory risk planning and mitigation. You will leads the Global Regulatory Sub-team (GRST) with key contributing members from a regional perspective, emerging markets, RA CMC as well as delivery & enablement.  You will be accountable for the delivery of all regulatory milestones including assessment of the probability of regulatory success together with risk mitigation measures.  You will be accountable for product maintenance, supply and compliance activities associated with marketed brands. 

You will lead the objective assessment of emerging data against aspirations and update senior management on project risks/mitigation activities.  You will partner with marketing company and regional regulatory affairs staff to influence developing views/guidance.  You will lead the regulatory staff working, provide leadership and participate in skill-development, coaching, and performance feedback. 

Typical Accountabilities:  

• Accountable for leading the development and implementation of the global regulatory strategy for a product/group of products of increasing complexity.  

• Ensure that the regulatory strategy is designed to deliver rapid approval with advantageous labeling in keeping with the properties of the product(s) and the needs identified by the business, markets and patients.  

• Demonstrate strategic leadership skills, and a deep understanding of global regulatory science and overall drug/biologic development processes and strategies for high profile, complex or novel development programs. 

• Lead the planning and construction of the global dossier and core prescribing information, conduct regulatory risk planning and mitigation, and lead the Global Regulatory Sub-team (GRST) with key contributing members from a regional perspective, emerging markets, RA CMC as well as delivery & enablement.   

• Accountable for the delivery of all regulatory milestones including assessment of the probability of regulatory success together with risk mitigation measures, potentially including product maintenance, supply and compliance activities associated with marketed brands. 

• Lead the objective assessment of emerging data against aspirations and update senior management on project risks/mitigation activities.   

• Partner with marketing company and regional regulatory affairs staff to influence developing views/guidance.   

• May line manage, develop, and coach Regulatory Affairs Directors (RAD) and/or Associate Regulatory Affairs Directors (ARAD) team members, and maintain and contribute to recruitment of staff to oversee team accountabilities.  

• Optional:May be accountable for leadership of regulatory operational activities from planning to submission of regulatory applications and HA interactions, providing regulatoryexpertiseand advice on procedural and documentation requirements to product teams and execution submission delivery plans across all regions.

Essential Skills/Experience

• A Bachelor’s degree in a scientific discipline, Regulatory Sciences, Pharmacy, or a related field.

• 10+ years experience of overall drug/biologic development processes and strategies for high profile, complex or novel development programs.

• Deep understanding of global regulatory science and integration with program strategy.

• Broad background of experience working in pharmaceutical business and prior experience in several areas within regulatory affairs.

• Proven experience leading regulatory, cross-functional teams, and stakeholder management.

• Successful leadership of at least one global regulatory marketing approval as GRL across major regions (US and EU) including leading response team and labeling negotiations.

• Ability to think strategically and critically and evaluate risks to regulatory activities.

• Previous experience in leading major Health Authority interactions.

• Excellent oral, written, and presentation skills.

• Strong organisational skills.

• Ability to work in a fast-paced environment in a hands-on fashion.

• Flexible and proactive, with the ability to manage multiple projects and successfully adapt to changing business needs and priorities.

Desirable Skills/Experience:

• Master's or PhD degree in a scientific discipline, Regulatory Sciences, Pharmacy, or a related field.

• Experience in the development or application of radio-conjugates would be highly advantageous.

• Experience with FDA advisory committee and CHMP oral explanation.

• Experience working on due diligence activities and in a business alliance environment.

• Experience in leading and growing people through coaching or mentorship.

• Contribution to non-project business initiatives (e.g. at a portfolio or cross functional level).

• Experience in Oncology (small molecules and biologics) is preferred.