Senior Director Regulatory Affairs at AstraZeneca Gothenburg

Published:
2018-12-18
City:
Göteborg, Västra Götalands län
Category:
Läkemedel, bioteknik & medicinteknik
Position:
Övrigt
Job type:
Heltid
Job type:
Konsultuppdrag
Reference number:
201192114
Last apply date:
2019-01-20
Contact:
Birgitta Nyström
Do you have extensive experience of Regulatory Affairs? We are currently looking for a Senior Director Regulatory Affairs for a 12 months consultant assignment at AstraZeneca.

At AstraZeneca, we lead our industry in the development of a strong and varied pipeline. This means our people are here to win, we give you a breadth of opportunities to be curious and do cutting edge, unique work that has significant impact on science and medicine.

The Global Regulatory Affairs Therapeutic area team is a strategic function and plays a key role within the Global Product Teams who work cross functionally to gather expertise and knowledge that informs our drug development programs. They are ultimately responsible for ensuring the pieces fit together to deliver for patients and physicians and provide therapy area regulatory expertise that supports regulatory interactions across the globe to secure fast submissions for our medicines in development.

Due to expansion, the Respiratory, Inflammatory and Autoimmune (RIA) team is currently seeking an experienced Regulatory Affairs Senior Director to join us for a one-year assignment starting in the beginning of 2019.

Description:
The Regulatory Affairs Senior Director is accountable for leading the development and implementation of the global regulatory strategy for a group of products of increasing complexity within the RIA portfolio and for ensuring that the strategy is designed to deliver rapid approval with advantageous labelling in keeping with the properties of the products and the needs identified by the business, markets and patients. The RA Senior Director possesses strategic leadership skills, has a deep understanding of global regulatory science and overall drug/biologic development processes and strategies for high profile, complex or novel development programs. Experience and knowledge of the one or more of the RIA disease areas is critical to being able to influence cross-functional discussions with Global Product Teams (GPT) and relevant stakeholders. The RA Senior Directors as the ability to take on the Global Regulatory Lead (GRL) role for a product/group of products and has the ability to function in dual capacity by delivering the overarching global regulatory strategy as well as serve as a regional lead based on their location, respectively.

Core Accountabilities/Responsibilities:

  • Leads the development and implementation of innovative global strategies of increasing complexity to maximize the likelihood of regulatory success.
  • Accountable for the delivery of all regulatory milestones including assessment of the probability of regulatory success together with risk analysis and mitigation measures.
  • Leads the planning and construction of the global dossier and core prescribing information
  • Accountable for product maintenance and compliance activities associated with marketed brands.
  • Serves as the single point of contact and Global Regulator Affairs (GRA) representative on Product Development Teams (PDT)/Global Product Teams (GPT).
  • Leads the Global Regulatory Sub-team (GRST) with key contributing members from a regional perspective, emerging markets, Reg CMC as well as delivery & enablement.
  • Partner with marketing company and regional regulatory affairs staff to influence developing views/guidance within leading Health Authorities on specific topics of relevance to their project or regulatory more generally.
  • Monitor changes in the regulatory environment, both general and specific to the therapeutic area and support and advise Global Product Teams (GPT) accordingly.
  • Capability to lead key cross-department or cross-functional projects on behalf of Global Regulatory Affairs (GRA) when necessary.
  • Provide regulatory leadership as needed in product in-license/due diligence review, product divestment and product withdrawal.
  • Participate in skill-development, coaching, and performance feedback of other regulatory staff working on the product/project.
  • Capability and credibility in complex, business critical projects and ability to cope with ambiguity and manage senior key stakeholders.
  • Has developed and actively uses external relationships with key stakeholders to reinforce AstraZeneca’s regulatory credibility.
  • Provide a regional focus and interact with commercial to understand business needs and to ensure regional commercial engagement with the proposed regulatory strategies
Requirements – Education and Experience:

  • Advanced degree in a science related field and/or other appropriate knowledge/experience.
  • Must have previous experience in leading Major Health Authority interactions (e.g. FDA advisory committee meetings, Oral explanations, Scientific Advice, Pre-NDA/BLA, EOP2 meetings etc.).
  • >10 years’ experience or equivalent of regulatory drug development including product approval/launch. Expert knowledge of regulatory affairs within one or more relevant therapeutic areas. In this case, any previous experience in vaccines/infectious disease is also useful.
  • Broad background of experience working in pharmaceutical business and prior experience in several areas within regulatory affairs, e.g. Global, European, International, Marketing Company or experience at a health authority.
  • Experience in relevant therapy area (small molecules & biologics) is preferred.
  • Proven leadership and program management experience.
  • Ability to think strategically and critically evaluate risks to regulatory activities.
  • Ability to work strategically within a complex and business critical development program.
  • Successful contribution to a major regulatory approval at a global level.
  • A scientific and clinical understanding of the regulatory sciences.
  • Must demonstrate competencies of: strategic thinking, strategic influencing, innovation, initiative, leadership and excellent oral and written communication skills.
Business: Dfind Science & Engineering

City: Gothenburg

Deadline for applications: 2019-01-18. Selection is on-going and interviews will be held continuously which means the position can be filled before deadline. Please make sure to send in your application at your earliest convenience.

For more information contact: Birgitta Nyström birgitta.nystrom@dfind.se or Malin Wåhlberg malin.wahlberg@dfind.se

Please keep in mind, e-mail applications will not be considered. Register your profile at Dfind Science & Engineering's webpage and send in your application there.

Organization/Business description:
Dfind Science & Engineering is a recruitment and consulting company within science and engineering. All our consultant managers and recruitment consultants have an education and work experience within the respective field. In combination with extensive knowledge of staff issues and solid experience of recruitment, this means that we understand our clients' need for both flexibility and the right skills.

Dfind Science & Engineering is since 2016 part of Randstad Group. With over 600 000 employees in over 40 countries Randstad is the world’s largest company within recruiting and staffing.