Global Regulatory Manager

Profile

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.

Global Regulatory Manager, Business Operations for Global Regulatory Strategy & Policy

Responsibilities


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


Qualifications/Requirements:


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.


Other Qualifications:


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.

Company: Bristol-Myers Squibb

Req Number: R1527358_EN

Updated: 2020-07-14 00:00:00.000 UTC

Location: Princeton,New Jersey

Bristol Myers Squibb is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, protected veteran status, pregnancy, citizenship, marital status, gender expression, genetic information, political affiliation, or any other characteristic protected by law.

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