Global Regulatory Manager, Regulatory Strategy & Policy
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.
Position: Global Regulatory Manager, Business Operations for Global Regulatory Strategy & Policy
Direct Manager: Head, Business Operations
Division: Regulatory Affairs
Location: Summit NJ
Direct Reports: N/A
About Bristol-Myers Squibb
Bristol-Myers Squibb is a global Biopharma company committed to a single mission: to discover, develop, and deliver innovative medicines focused on helping millions of patients around the world in disease areas such as oncology, cardiovascular, immunoscience and fibrosis.
Join us and make a difference. We hire the best people and provide them with a work environment that places a premium on diversity, integrity, collaboration and personal development. Through a culture of inclusion, we create a better, more productive work environment. We believe that the diverse experiences and perspectives of all our employees help to drive innovation and transformative business results.
- Support Regulatory Lead in the preparation of HA interactions (meeting preparation, rehearsals, execution, follow-up, minutes, etc.)
- Maintain tracking data for health authority meetings, PMRs/PMCs, and other key regulatory milestones and liaise cross-functionally to generate periodic internal milestone reports
- Provide operational support on strategic regulatory documents to help drive timely deliverables
- Drive operational excellence in Global Regulatory Strategy & Policy through projects aimed to support collaboration and improve efficiency
- Additional responsibilities, in conjunction with regional and/or global regulatory leads, include:
- IND, BLA, and NDA maintenance submissions
- Safety and Annual report submissions (regulatory components)
- Coordinating and driving rapid response team meetings to ensure quality and timely responses to health authority queries. This includes the preparation of response to HA queries according to the rapid response process.
- Maintaining global submission plans and supporting those plans can be executed on time
- Coordinating and driving global regulatory subteam meetings to ensure high quality meeting discussions & outputs; this includes diligent follow-up with Subteam members to uphold accountabilities and drive decision-making
- Solid scientific background (BS, MS, PhD, PharmD, in life sciences, chemistry, pharmacy, medicine or veterinary).
- 1-3 years of pharmaceutical industry experience. Ideally 1 year in regulatory affairs or 2-3 years in a complementary functional area (eg, clinical research)
- Working knowledge of regulatory procedures (US or other)
- Demonstrates a high-level of self-motivation and professional commitment. Indirect management experience of people or major projects.
- Ability to rapidly adapt to different issues and projects at one time. Good interpersonal skills.
- Excellent communication skills.
- Comprehensive understanding of the pharmaceutical industry.
- Comfortable working in a fast-paced environment where speed is paramount
- Willing to work as a topic expert, outside of a traditional functional environment, in a team unified around serving the assets
- Ability to recognize, articulate, and accept calculated risks to make informed decisions
- Willingness and ability to effectively work in a highly matrixed team environment
- Develop understanding of different TAs due to assignment to different projects.
- Increased understanding of the regulatory procedures (US, EU, others) and regulatory landscape.
- Increased exposure to global and multi-functional teams.
- Strong team player with ability to seamlessly collaborate across functional and geographic boundaries to achieve company’s goals
- Strong attention to detail
- Thrives on seeking and incorporating constructive feedback
- Communicates opinions, facts and thoughts with clarity, transparency and honesty
- Demonstrates ownership of results within (and beyond) area of responsibility.
- Sets clear and high expectations and holds self and others accountable for decisions and results achieved.
- Looks for opportunities for continuous improvement.
Around the world, we are passionate about making an impact on the lives of patients with serious diseases. Empowered to apply our individual talents and diverse perspectives in an inclusive culture, our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.
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.
Learn more here
Job posted: 2020-09-01