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Represent Medical Strategy function of the assigned product and maximize the product value and patient benefit through Medical Plan development and implementation.
UMN:
1) Continuously identify Unmet Medical Needs (UMN) related to assigned Therapeutic Area products based on the regular dialogue with Thought Leaders (TL), advisory board meetings, published information (domestic/overseas books/journals/congresses) and other available information.
2) Ensure that the local and global medical plans are consistent with UMN
Medical Plan and Expertise:
1) Develop Medical Strategy and Plan to address UMN by integrating data generation, publication, advisory boards, TL engagement, medical education, and any additional activities accompanied by a concrete budget plan. Update the Medical Plan at budget update cycle.
2) Clearly explain the Medical Plan and ensure alignment with multiple stakeholders in BMSKK as well as Global Medical.
3) Completely understand internal procedural documents (PD), other relevant rules, laws and regulations in Japan. Assure that Medical plans and its implementation comply with these rules/regulations/laws.
4) Lead medical matrix team for Medical Plan development and implementation. Appropriately align each activity with the Brand Team activity.
5) Provide adequate scientific support for internal stakeholders.
TL Engagement:
1) Conduct scientific exchange and maintain trustful relationship with select TLs in compliant with related PD.
2) Collect medical insights through the scientific dialog, verify the medical hypothesis and solidify the Medical strategy and Plan to ensure its alignment with clinical reality
3) Track and keep the record of TL interactions in compliant with related PD.
Data Generation:
1) Identify data gap for the assigned Therapeutic Area product between the available data and ideal data set to satisfy the UMN, to promote appropriate use of the assigned product, and to maximize the patients' benefit.
2) Under the oversight of Medical Director, strategically and creatively develop a data generation plan to fill the data gap taking feasibility, scientific adequacy, and ethical considerations into account.
3) Explain, discuss and align the data generation plan with internal stakeholders (global medical, brand team, etc.)
4) Implement the data generation plan including ISR request handling (interface to investigators, representative of BMSKK toward global team).
5) Keep tracking the progress and update the data generation plan.
Publication:
1) In collaboration with relevant internal functions, strategically develop a publication plan of the assigned Therapeutic Area product including original papers and congress presentations focusing on company-sponsored clinical trials and get endorsed from the governance bodies.
2) Implement publications with targeted schedule. This includes story building, communication with external/internal authors and reviewers as well as medical writer, contents validation, and on-time delivery of the publication.
3) Update the publication plan according to the clinical trial progress, UMN and competitive landscape.
Advisory Boards:
1) Collect TL insights by planning and conducting Advisory Boards to identify, confirm and fulfill UMN around assigned Therapeutic Areas product, in a completely compliant manner with related procedural documents (PD).
Medical Education:
1) Identify the needs for medical education based on UMN to advance the therapy, science and appropriate understanding of the assigned Therapeutic Area product.
2) Plan on medical educational meetings/printed materials/other communications considering adequacy and feasibility, and implement them.
Degree Requirements
1) Advanced scientific degree in medical/pharmaceutical/veterinarian/life-science area
2) Preferably with first author for at least an original paper (PubMed-cited level) and a congress presentation
Experience RequirementsSolid experience in Medical Affairs in Japanese industry Solid field experience (e.g. MSL) and trustful interactions with TLs in hematological malignancies
1) At least three-year experience of medical, pharmaceutical or life-science field
2) At least two years of experience in the area of hematological malignancies
Key Competency Requirements
Knowledge
1) Knowledge of hematological malignancies (disease mechanism, epidemiology and typical treatment in Japan) at specialized physician's level.
2) Knowledge about Promotion Code and any other applicable regulations to Medical Affairs in Japan.
3) Preferably with knowledge of clinical research, clinical development (Ph1-4), ISRs, Japanese PMS.
Skills
1) Proven leadership with collaborative mindset in team coordination and project delivery
2) Strong communication, presentation and negotiation skills as a professional in Japanese context, ability to build and maintain reliable customer relationships
3) Skills to analyze data and information, identify needs/risks, translate them into actionable plan, and implement it with regular monitoring and issue management.
4) Team management skills to lead a team, nurture trust and confidence among members, and identify and address issues in a team.
5) Operationally efficient and able to liaise with stakeholders from all levels both internally and externally
Language proficiency
1) Complete level of written Japanese – can completely understand medical articles and general business documents in Japanese, can write formal Japanese at business setting, and can write a medical article in the assigned area.
2) Complete level of oral Japanese – can make presentations, have medical discussions and build an trustful and appropriate relationship with HCPs.
3) Advanced level of written English – can completely understand medical articles of assigned area and general business documents in English
4) Advanced level of oral English – can make effective presentations, have discussions and negotiations with global counterparts in English
Travel Required
HCP/HP visit/several times a month, if requested
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 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.
If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information:
Data Protection
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Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.
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R : Senior Manager, Medical Lead, Hematology Medical-
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