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.
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. Read more at careers.bms.com/working-with-us
Key Responsibilities
* Provides oversight over a complex program for one or more Therapeutic Area (TA)(s), or high-priority asset(s) and working closely with their stakeholders.
* Ensures that labeling strategies align with the regulatory requirements globally and managing relationships with senior stakeholders.
* Mentors and develops team members to foster a high performing culture, as applicable.
* Ensures that Program Deliverables are met and labeling claims across program / TA are consistent.
* Leads key initiatives (Process Improvements, Development of new tools, technologies) to support efficient global label development and worldwide submissions and approvals.
* Serves as primary contact for Labeling Strategy Team (LST), e.g., Global Regulatory Lead (GRL), Safety Management Team Lead (SMTL), Functional SMEs, Documentation Leads and Medical Writer, Dossier Lead and Submission Manager, also serves as interface for Country Regulatory Managers to support timely and quality submissions globally.
* Drives labeling strategy in partnership with the Global Regulatory Team Leader in line with the overall regulatory Strategy by providing labeling expertise (labeling regulations, internal processes, and competitor analyses) for CCDS, USPI and SmPC (Centralized / Mutual Recognition / Decentralized Procedure) and Target Product Labeling, as applicable.
* Identifies opportunities to influence regulatory policy and climate with respect to labeling content.
* Coordinates labeling activities of multifunctional contributors, reviewers and approvers and manages the label review and approval process to maximize speed and quality.
* Ensures effective planning of all cross-functional labeling activities.
* Reviews country labels to ensure labeling compliance and assess labeling differences to CCDS.
* Supports responses to labeling related inquiries from Global Health Authorities and related to inspection activities.
Degree Requirements
Masters of Life Sciences or equivalent, with thorough understanding of scientific principles and at least 10 years of Labeling (CCDS / USPI / SmPC) / Regulatory Experience; Bachelor of Life Sciences with at least 15 years of Labeling / Regulatory Experience; has at least experience with one NME submission globally.
Key Competency Requirements
* Knowledge of Global Labeling Guidances, Drug Development and Commercialization of prescription medicines.
* Proven understanding of the dynamics and purpose of the Company Core Data Sheets (CCDS) and the implications of the CCDS.
* Proven ability to understand regulatory implications of product strategy related to labeling development, assessment, and management.
* Demonstrated ability to develop strong and positive working relationships across diverse teams and within a global environment.
* Proven Matrix leader with excellent problem-solving skills.
* Ability to influence and lead a diverse group of Subject Matter Experts from a variety of disciplines and facilitate discussions and decision making.
* Proven ability to develop and manage a highly competent and technically skilled team.
* Experience in managing high to medium complex projects.
* Excellent verbal and written communication skills.
* Keen attention to detail and accuracy.
* Ability to assimilate clinical and scientific information and present it in a concise manner.
* Ability to think creatively and possess excellent problem-solving skills.
Ideal Candidates Would Also Have
* Advanced Academic Training (PharmD, PhD, MD) highly desirable.
If you come across a role that intrigues you but doesn’t perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.
Uniquely Interesting Work, Life-changing Careers
With a single vision as inspiring as Transforming patients’ lives through science, every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in an inclusive culture, promoting diversity in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion, and integrity bring out the highest potential of each of our colleagues.
On-site Protocol
BMS has a diverse occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role.
Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles, the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.
BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments, and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to adastaffingsupport@bms.com. Visit careers.bms.com/eeo-accessibility to access our complete Equal Employment Opportunity statement.
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 boosters.
BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.
Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.
Bristol Myers Squibb is Disability Confident – Employer.
A UK Government scheme.
#J-18808-Ljbffr