Otsuka Pharmaceutical Development & Commercialization, Inc. (OPDC) ensures full integration of development and commercialization activities, from initiation of the clinical program for a compound through product positioning and global life cycle management, which will lead to globally consistent branding of our products.
Otsuka is seeking a Director/Senior Director, Global Medical Affairs (CNS) who will be responsible for the medical affairs activities associated with the development and commercialization of new products, including bringing commercial input to the clinical team and clinical input to the commercial team. The individual acts as a driving force in the public dissemination of information and data, including product labeling and promotional materials.
The specific responsibilities assigned to the Director/Senior Director, Global Medical Affairs include:
Plans commercial strategies for clinical study designs and product life cycle development.
Proactively acts as a liaison between the commercial group and the clinical development organization.
Develops, produces, and organizes manuscripts, presentations, international symposiums, and posters.
Interacts with experts in the field to obtain feedback on products and source appropriate faculty to give presentations on behalf of the company.
Provides input into the creation of marketing materials and ensures data is accurately and effectively communicated.
Provides input into regulatory documents.
Provides input on feasibility of the product during pre-clinical and clinical studies.
Administers continuing education and unrestricted grants when necessary.
Participates in the evaluation of potential in-licensing candidates.
The successful candidate must meet the following minimum requirements:
MD or PhD with a minimum of 5 years of experience in the industry.
Requires extensive understanding of the company's products, commercialization strategy, the competition, and the pharmaceutical industry in general.
Maintains a current awareness of new drug developments in targeted therapeutic areas.
Strong scientific background and solid understanding of the pre clinical and clinical development processes.
Solid statistical knowledge with a demonstrated ability to interpret study findings and communicate appropriately.
Ability to interpret scientific data and calculate potential commercial value and financial impact.
Skilled in managing and influencing people
Strong computer skills with demonstrated experience in working with the Microsoft suite of programs (Word, Excel, PowerPoint, and Outlook).
Demonstrated experience working with secondary data sources.
Demonstrated ability to effectively communicate (written information and presentations) with internal and external parties.
Ability to travel 25-30% of the time globally.
We offer a competitive compensation and benefits package plus a positive work environment, which encourages personal growth and achievement.
