Vice President, Regulatory Affairs, Europe and International
vor 2 Wochen
BeOne continues to grow at a rapid pace with challenging and exciting opportunities for experienced professionals. When considering candidates, we look for scientific and business professionals who are highly motivated, collaborative, and most importantly, share our passionate interest in fighting cancer.
General Description:
The Vice President, Europe and International Regulatory Affairs (APAC and New Markets, excluding USA, China and Japan), is a leadership position that will be responsible for building and leading the regulatory groups to develop and implement regulatory strategies to secure and maintain market access for product(s) in line with business objectives and in coordination with key internal stakeholders. The incumbent will provide leadership and strategic regulatory oversight for BeOne/Beigene projects ensuring that the latest regulatory requirements and standards are met. The individual has departmental and corporate level responsibility for regulatory strategy, will sit on the GRA leadership team and represent regulatory on the European cross functional leadership team. Externally, the individual will interface with EMA, national regulators and international organizations regarding drug development and registration strategies and provide insights to the organization of evolving regulatory policy and its impact to BeOne/Beigene's business. He/She also has line management, people development, and performance management responsibility across a broad geographic area.
Essential Functions of the job:
Establishes, develops, and manages effective/high performance regulatory groups and teams both via direct and indirect reporting structure
Builds partnerships with key stakeholders to ensure that strategic business goals are met through the sharing of knowledge and expertise
Establishes and maintains a trusting relationship with the Regulators by enforcing transparency in communications and ensuring compliance with national regulations
Leads the regulatory team by creating a supportive environment that enables and empowers team members to collaborate and deliver high quality work
Provides high level strategic and operational regulatory direction and mentorship on projects including, but not limited to, general regulatory strategies, regulatory requirements for clinical studies and Marketing authorizations, regulatory strategic development plans and risk assessments, critical issue management and advice on Health Authority interaction strategies.
Applies extensive knowledge of drug development and regulatory requirements both strategically and operationally to development projects and marketed products to support corporate goals and improve global regulatory processes.
Maintains up-to-date regulatory knowledge, state-of-art regulatory science, and deep understanding of regulatory policy globally, and assesses the impact on business and product development strategy.
Ensures RA's contribution to high quality of CTA's and MAA's in conformance with national regulatory requirements, and to the timely submission and approvals
Support the establishment of new affiliates aligned with BeOne/BeiGene's geographic footprint.
Support the development and execution of local country regulatory strategy and life cycle management.
Leverages new technologies and regulatory mechanisms to enable efficient submissions with a fungible team that supports the local markets robustly with new and evolving processes to be defined.
Core Competencies, Knowledge & Skill Requirements:
Thorough understanding of drug development process and the pharmaceutical industry and healthcare environment including regulatory requirements and policy trends in Europe and other markets, preferably with a strong oncology focus.
Extensive regulatory experience with INDs/CTAs, NDAs/BLAs/MAAs, lifecycle management, interactions with Health Authorities, developing and implementing regulatory strategies with a proven track record of significant regulatory accomplishments.
Strong business acumen and ability to make sound decisions that contribute positively to the business
Very strong strategic skills including creativity and effectiveness in identifying and addressing major strategic challenges (e.g. new competition, shifting market environment) and the ability to balance short-term needs with long-term vision
Proven ability to deliver on goals within a cross-functional team/partnership environment with a high level of professionalism
Willingness to explore the use of new technologies and processes to streamline deliverables.
Strong leadership of people and ability to lead a diverse team virtually for high performance
Communication & Interpersonal Skills:
Excellent verbal and written skills; able to analyze, define, and effectively convey difficult and complex issues in a way that accurately and persuasively communicates the issues to be internal and external stakeholders
Skilled in conflict resolution/negotiation. Fosters open communication. Listens and facilitates discussion.
Strong negotiating skills and ability to think creatively and develop creative solutions
Proven ability to build trust and respect within the organization.
• Ability to prioritize and handle multiple projects simultaneously.Interacts with external business partners and regulatory
Supervisory Responsibilities:
Yes
Computer Skills:
Microsoft office applications, Internet, Access to internal portals (e.g., Veeva Vault), Access to external portals (e.g., EMA portals), use of AI and other emerging tools
Other Qualifications:
NA
Travel:
When needed
Global Competencies
When we exhibit our values of Patients First, Driving Excellence, Bold Ingenuity, and Collaborative Spirit, through our twelve global competencies below, we help get more affordable medicines to more patients around the world.
- Fosters Teamwork
- Provides and Solicits Honest and Actionable Feedback
- Self-Awareness
- Acts Inclusively
- Demonstrates Initiative
- Entrepreneurial Mindset
- Continuous Learning
- Embraces Change
- Results-Oriented
- Analytical Thinking/Data Analysis
- Financial Excellence
- Communicates with Clarity
We are proud to be an equal opportunity employer. BeOne does not discriminate on the basis of race, religion, color, sex, gender identity, sexual orientation, age, disability, national origin, veteran status or any other basis covered by appropriate law. All employment is decided on the basis of qualifications, merit, and business need.
-
Basel, Basel-Stadt, Schweiz BeOne Medicines Vollzeit CHF 120'000 - CHF 180'000 pro JahrBeOne continues to grow at a rapid pace with challenging and exciting opportunities for experienced professionals. When considering candidates, we look for scientific and business professionals who are highly motivated, collaborative, and most importantly, share our passionate interest in fighting cancer.The Senior Director, Government Affairs & Public...
-
Basel, Basel-Stadt, Schweiz BeiGene Vollzeit CHF 120'000 - CHF 180'000 pro JahrBeOne continues to grow at a rapid pace with challenging and exciting opportunities for experienced professionals. When considering candidates, we look for scientific and business professionals who are highly motivated, collaborative, and most importantly, share our passionate interest in fighting cancer.The Senior Director, Government Affairs & Public...
-
Basel, Basel-Stadt, Schweiz Ultragenyx Pharmaceutical VollzeitWhy Join Us? Be a hero for our rare disease patients At Ultragenyx, we fundamentally believe that taking real impactful action to care for the needs of patients and our people is always the right thing to do. To achieve this goal, our vision is to lead the future of rare disease medicine. For us, this means going where other biopharma companies won't...
-
Regulatory Contractor
vor 1 Woche
Basel, Basel-Stadt, Schweiz Barrington James Vollzeit CHF 60'000 - CHF 120'000 pro JahrJob DescriptionRegulatory Contractor – full-time 6 months contract (remote)We are seeking a Regulatory Affairs Contractor to support one of our small biotech clients, including the preparation and submission of initial Marketing Authorization Applications (MAAs).September start dateFully remote, but preference to have candidates based in Spain, Poland or...
-
Regulatory Contractor
Vor 7 Tagen
Basel, Basel-Stadt, Schweiz Barrington James Vollzeit CHF 90'000 - CHF 120'000 pro JahrRegulatory Contractor – full-time 6 months contract (remote)We are seeking a Regulatory Affairs Contractor to support one of our small biotech clients, including the preparation and submission of initial Marketing Authorization Applications (MAAs).September start dateFully remote, but preference to have candidates based in Spain, Poland or Switzerland.Key...
-
VP Sales Nutrition Europe
Vor 7 Tagen
Basel, Basel-Stadt, Schweiz Actylis VollzeitActylis is a global solutions provider with over 75 years of experience, specializing in streamlining the management of critical ingredients and raw materials for our business partners.We offer both sourcing and manufacturing solutions tailored to meet diverse and evolving needs, ensuring a reliable, agile, and secure supply network. Our commitment to...
-
Regulatory Affairs Manager 50
vor 2 Wochen
Basel, Basel-Stadt, Schweiz gloor&lang AG Vollzeit CHF 80'000 - CHF 100'000 pro JahrInnovative Produkte hautnah - Region BaselUnser Kunde ist ein pharmazeutisches Familienunternehmen in der Health Care Branche im Grossraum Basel. Der Hauptsitz und Standort in der Schweiz forscht, entwickelt und produziert ein hochwertiges Produkteportfolio. Davon zählen einige Präparate in der Schweiz zu den Marktführern. Die Produkte werden klinisch in...
-
VP Operations Non-clinical development and CMC
vor 2 Wochen
Basel, Basel-Stadt, Schweiz FimmCyte Vollzeit CHF 120'000 - CHF 180'000 pro JahrThe JobAt FimmCyte Therapeutics, an innovative leader in biotech, we are seeking a dynamic and experienced Vice President of Operations focusing on advancing a novel molecule from development candidate to IND approval and beyond. Our company, with a close-knit team is committed to advancing cutting-edge therapeutics for large unmet needs. As VP of...
-
Regulatory Affairs CMC Manager, Drug Substance, ADC
vor 2 Wochen
Basel, Basel-Stadt, Schweiz Barrington James Vollzeit CHF 105'000 - CHF 120'000 pro Jahr**Must be based/willing to travel to Basel, Switzerland4 days on site / 1 day remote**Salary range: 105K–120K CHFResponsibilitiesLead Drug Substance (DS) CMC regulatory activities, focusing on antibody–drug conjugates (ADCs), chemical payloads, and bioconjugates.Author and review clinical regulatory submissions from scratch (IMPD/IND, CTD Modules 2 &...
-
Medical Affairs Cluster Lead LCM
vor 1 Tag
Basel, Basel-Stadt, Schweiz Mundipharma VollzeitMedical Affairs Cluster Lead LCMLocation: Switzerland / AustriaDepartment: Medical AffairsJob type: PermanentJoin us and make a difference when it matters mostAt Mundipharma, we are proud of the work we do to bring innovative treatments to patients. We challenge ourselves constantly to deliver more for patients, healthcare professionals, our partners, and...