Associate Director, Eu Regulatory Strategy Oncology
vor 2 Wochen
At Bristol Myers Squibb, we are inspired by a single vision - transforming patients’ lives through science. In oncology, hematology, immunology and cardiovascular disease - and one of the most diverse and promising pipelines in the industry - each of our passionate colleagues contribute to innovations that drive meaningful change. We bring a human touch to every treatment we pioneer. Join us and make a difference.
**The Role**
Bristol Myers Squibb is looking to recruit an **Associate Director, EU Regulatory Strategy Oncology **based in Boudry, Switzerland or Uxbridge, UK.
**Key Duties and Responsibilities**:
- Integrates the European regulatory, legal, scientific/medical and business perspectives to achieve the optimal regulatory outcomes for assigned project(s) in accordance with company objectives.
- Translates strategy into operational goals and objectives, identifies resources and leads the organization to focus on objectives. Assures that organization follows through to achieve high quality execution of plans.
- Ability to contribute and add value to the writing of scientific documents for regulatory purpose.
- Able to act as Contact Person for assigned project(s) with EMA in line with BMS strategy and to provide strategic directions and supervise negotiations with other relevant regulatory agencies for assigned project.
- Provides direction for maximizing opportunities within projects (eg. lifecycle) and across the geographical area to support the productivity priorities.
- Participates actively in and represents GRS-EU for their project(s) in the Global Regulatory Team and on various multi-functional committees or teams.
- Communicates actively and timely with Global Regulatory Sciences colleagues in European countries, including through direction of European Regulatory Teams.
- Active participation in regional organizational activities for the Liaison function (across projects)
- Develops strong working relationships with key stakeholders both within and outside the company.
- Builds and maintains strong relationships with alliance partner when applicable.
- Watches, anticipates and acts on trends and changes in the European and international regulatory environment which may impact on the business.
**Qualifications, Knowledge and Skills** Desired**:
- Strong scientific/medical background.
- Understanding of pharmaceutical product development
- Understanding of European regulatory principles and their impact on company’s development and business
- Understanding of the complexities of cross functional management issues
- Understanding of legal and business aspects related to European regulatory procedures and outcomes.
- Compatible with BMS vision and culture.
**Why you should apply**
- You will help patients in their fight against serious diseases
- You will be part of a company that encourages excellence and innovation, respects diversity, develops leaders and values its employees.
- You’ll get a competitive salary and a great benefits package
- Bristol Myers Squibb has been certified as a Great Place to Work in Switzerland Each day, our collaborative teams come together to support some of the most interesting work of their careers.
**#LI-Hybrid**
Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives.
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