Executive Director/vice President

vor 3 Wochen


Boudry, Schweiz Bristol Myers Squibb Vollzeit

**Working with Us**
Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You’ll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams rich in diversity. Take your career farther than you thought possible.

Job Title: Executive Director/Vice President - International Patient Safety

The Worldwide Patient Safety group is responsible for ensuring the safety of our medicines globally.

The International Team is responsible for robust, compliant and consistent safety management and risk management across all territories BMS operates in, ensuring compliance with global and local regulations and requirements.
- Ensures integrity and compliance of the in-country Worldwide Patient Safety function; Oversees the conduct of pharmacovigilance functions and activities within all countries where BMS operates
- Ensures International regulatory compliance with safety across all International Local Market (LM) offices
- Translates strategy into operational endpoints to build and shape the International Patient Safety function and its capabilities
- Ensures productive and effective integration of International within WWPS Global
- Ensures the efficient and effective deployment of Global programs and initiatives at the Regional / Local level
- Evaluates, optimizes, develops and integrates processes, systems and policies as they relate to International Patient Safety
- Oversees the execution of effective risk management programs
- Partners with General Managers and relevant local staff to support local market needs
- Ensures effective, strong and productive relationships and working interfaces between Patient Safety and other functions
- Ensures effective and consistent communication of issues relating to product safety across all territories
- Ensures excellent and timely support for safety issues & enquiries impacting the international region; oversees the management of responses to International regulatory authority safety enquiries.
- Ensures inspection readiness plans are in place and that any inspection issues/findings are adequately addressed
- Oversees of International Patient Safety budget
- Recruits, hires, and develops staff
- Ensures that appropriate resources are in place within the countries of the region to meet current and future business needs.
- Drives career development of the Local Patient Safety staff to build and maintain a high-performance team. Identifies, recruits and retains talent.
- Ensures staff are trained effectively to perform their roles and
- responsibilities and drives functional excellence
- Is part of WWPS Leadership Team

Degree Requirements:

- 10 years minimum of pharmaceutical experience in patient safety
- Preferred: Experience in medical affairs, international regulatory experience

Key Competency Requirements:

- Demonstrated ability and experience leading high-performing teams in a highly matrixed and collaborative environment; experience with remote management and oversight,
- Knowledge of pharmacovigilance as well as emerging trends/directions in pharmacovigilance
- Ability to advise and direct senior leaders in International on evaluation of safety concerns and minimization of patient risk throughout the life cycle of a drug product
- Capable of influencing in a complex matrix environment and exhibiting productive matrix behaviors as a role model for their employees
- Excellent understanding of the markets. Utilizes this knowledge to provide
- input to Global initiatives and identify opportunities to enhance the pharmacovigilance/patient safety functions.
- Excellent ability to communicate, specifically on scientific topics
- Able to integrate knowledge and experience in multiple domains (e.g. pharmacovigilance, risk management, medical affairs, drug regulations, drug development, commercial, etc.)
- Proven experience of interactions with relevant Regulatory Authorities, eg FDA, EMA, MHRA, PMDA, TGA, other

Travel Required (nature and frequency):

- Regular travel to relevant BMS sites and US HQ ( up to 35%)

**Uniquely Interesting Work, Life-changing Careers**

**On-site Protocol**
Physical presence at the BMS worksite or physical presence in the field is a necessary job function of this role, which the Company deems critical to collaboration, innovation, productivity, employee well-being and engagement, and it enhances the Company culture.

BMS cares about your well-being and the well-being of our staff, customers, patients, and communities. As a result, the Company strongly recommends that all employees be fully vaccinated for Covid-19 and keep up to date with Covid-19 booste



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