Sr. Manager, Central Access

Working with Us
Challenging. Meaningful. Life-changing. Those arent 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. Youll get the chance to grow and thrive through opportunities uncommon in scale and scope alongside high-achieving teams. 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: Job Responsibilities

1. Policy Research and Strategic Planning

• Closely track the policy dynamics of central ministries and commissions such as the National Healthcare Security Administration (NHSA) and the National Health Commission (NHC) as well as relevant industry associations and academic societies. Focus on core areas including dynamic adjustments to the National Reimbursement Drug List (NRDL) medical insurance payment method reforms national drug price negotiations and centralized procurement. Conduct in-depth interpretation of policy orientations implementation rules and industry impacts and form professional policy briefings and in-depth research reports to provide accurate basis for the decision-making of the Head of Central Market Access and the formulation of the companys overall strategy.

• Combine the characteristics of the companys product pipeline (oncology hematology immunology cardiovascular and other fields) assist in participating in the formulation of medium and long-term central market access strategies and annual implementation plans clarify access goals core paths and resource allocation plans align with the companys dual innovation strategy and ensure that access strategies are aligned with the companys R&D and commercial layout.

• Anticipate opportunities and risks brought by policy changes formulate response plans in advance avoid policy compliance risks in the access process and proactively put forward suggestions for policy formulation to help create a favorable external policy environment for the industry and the company.

2. Full-Process Management of Central Medical Insurance Access

• Be responsible for the full-process work of national medical insurance catalog declaration and price negotiation for the companys core products and new indications including preparation of application materials coordination of pharmacoeconomic research formulation of negotiation strategies follow-up of negotiation process and connection of post-negotiation implementation. Ensure the achievement of the companys NRDL access goals promote the rapid inclusion of innovative products into medical insurance and improve patient access.

• Coordinate internal and external resources link with R&D Medical Affairs Marketing Finance and other departments to complete the collation of clinical evidence cost data calculation value proposition refinement and other work required for medical insurance negotiations ensuring that the application materials are compliant complete and competitive.

• Be responsible for the maintenance of the product price system after medical insurance negotiations and the follow-up of the implementation of medical insurance payment policies. Cooperate with relevant departments to conduct medical insurance policy interpretation and internal sharing and promote the transformation of medical insurance access achievements into market performance.

3. Establishment and Maintenance of External Relationships

• Be responsible for the coverage and maintenance of core central-level stakeholders including the National Healthcare Security Administration and its affiliated institutions relevant industry associations and academic societies and core experts. Establish stable and mutually trusting cooperative relationships through professional communication and academic exchanges and build a platform for policy advocacy and value transmission.

• Participate in various activities organized by industry associations and think tanks actively convey the companys innovative concepts and product value participate in industry policy discussions enhance the companys industry influence in the field of central market access and create a good external cooperative environment for the company.

• Overall manage external cooperative institutions (such as consulting companies and research institutions) to ensure that the policy research pharmacoeconomic analysis and other services they provide meet the companys needs and support the efficient advancement of access work.

4. Other Special Work

• Regularly report the progress of access work policy dynamics existing problems and solutions to the Head of Central Market Access ensuring timely and accurate information transmission to support the efficient decision-making of the responsible person.

• Be responsible for the collection collation and analysis of central market access-related data establish a complete access database and provide data support for work review and strategy optimization.

• Complete other central market access-related special work assigned by the responsible person to help achieve the overall goals of the department.

Job Qualifications

1. Educational Background

• Bachelors degree or above; majors in Medicine Pharmacy Public Health Health Economics Public Administration and other related fields are preferred; masters degree or above is preferred.

2. Work Experience

• More than 5 years of relevant work experience in central market access in the pharmaceutical industry; more than 3 years of work experience in core central market access positions in multinational pharmaceutical companies (MNCs) is preferred.

• Possess full-process practical experience in national medical insurance catalog declaration and price negotiation; those with successful cases of promoting innovative products into the National Reimbursement Drug List (NRDL) are preferred; those familiar with the relevant work processes of centralized procurement in the pharmaceutical industry will be given extra points.

• Possess rich resources of central-level government departments industry associations academic societies core experts and other stakeholders with a good foundation for cooperation and communication channels.

• Possess excellent team spirit be able to cooperate with the responsible person in team management and cross-departmental collaboration and be willing to share experience and help the team grow.

• Possess good pressure resistance be able to adapt to a fast-paced and high-demand working environment and efficiently complete various work tasks.

• Possess certain English listening speaking reading and writing skills; those who can read English professional literature and connect with global relevant personnel are preferred.

If you come across a role that intrigues you but doesnt 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 a supportive culture promoting global participation 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 an 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.

Supporting People with Disabilities

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 . Visit to access our complete Equal Employment Opportunity statement.

Candidate Rights

BMS will consider for employment qualified applicants with arrest and conviction records pursuant to applicable laws in your area.

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