Job Description
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Core Mission
Align with global strategies to develop China local medical strategy and tactical plan for Galderma products/portfolios, including but not limited with pre-launch preparation, post-marketing clinical trials, scientific communication, build up and maintain academic relationship with top KOLs. At the same time, to provide medical/academic insights for marketing strategy/plan and cross-functional professional support.
Requirements
Education/Training:
- Master of clinical medicine, bio-pharmaceutical or biotechnology as minimum.
Work Experience:
- More than 2 year in clinical practice is preferred;
- More than 3 years in pharmaceutical or medical device or cosmetic company, including 2 year medical strategy role, early product launch experience is preferred, specialized in dermatology is preferred;
Required pre-requisites skills/experience for this position:
- Firmly grounded in scientific fundamentals of clinical study protocol development and methodology, data interpretation and scientific communication. Being able to handle clinical studies individually, preferred if multi-center trial experience is in place.
- Capable of thinking holistically, with solid understanding of Galderma portfolio, to develop Central Medical Strategy and tactics of specific product.
- Business insights and marketing sense (good understanding pharmaceutical business)
- Ability to function in a team-oriented (matrix) environment.
- Ability to think strategically to guide publication-related activities in accordance with industry standards and good publication practices, followed by proper data dissemination.
- Fluent English in literature reading, medical writing and oral communication, can independently communicate with global team.
- Excellent Project management skills and Budget control.
- Travel Frequencyï¼> 15%
Duties and Responsibilities
Main Duties
- Develop central medical strategies for assigned product(s), with the holistic consideration of the portfolio, execute medical activities with good quality based on approved medical strategies.
- With high strategic thinking, develop scientific stories, presentations and other tools in accordance with strategy.
- Provide up to date disease and product knowledge to internal and external customers for assigned product(s).
- Provide scientific support to pre-launch registration, make sufficient launch readiness to achieve launch excellence.
- Provide medical and scientific support to the Companyâs marketing and sales activities, including input in marketing strategy from medical point of view, round tables, symposia and medical education activities, liaison with opinion leaders, scientific communications, sales training, and medical input in promotional materials.
- Develop and maintain permanent relations with a network of Key opinion leaders and experts for the assigned product(s) in order to maintain and reinforce the scientific position of the Group.
- Review and approval promotional and non-promotional materials, ensure appropriate scientific and medical compliance.
- Medical Affairs Projects and Studies
- Develop integrated data generation strategy and responsible for the whole process of execution of clinical study in align with GCP, Local regulations, including contract, payment and publication.
- Be responsible for approval process (Local, Global, and Central EC) approval for clinical studies, including Phase IV Studies, PMS, IIT and RWE.
- Lead and oversee the whole process of medical affairs studies, responsible for the database management, CSR and publication process.
- Lead and oversee medical projects, at the mainwhile, maintain compliance and excellent budget management.