JOB WEIGHTING:

Job Weighting%

Main Responsibilities

40%

•Responsible for all medical affairs activities in the therapeutic area.

40%

•Responsible for scientific exchange with external experts in the therapeutic area

20%

•Responsible for recruiting, coaching, managing MSL for team development and medical strategy execution

REQUIREMENTS:                  

• Medical Degree, MD or PhD is a plus.
• Strong background in clinical practice
• Suitably qualified individuals from a scientific background and relevant experience will also be considered in exceptional circumstances
• Previous medical affairs pharmaceutical or biopharmaceutical industry experience is essential
• A demonstrated understanding of drug development and commercialization processes, have sound and current knowledge of the regulatory environment, significant experience in overseeing or conducting clinical trials, a solid understanding of trial design and methodology and an understanding of the need to balance safety and efficacy concerns.
• A demonstrated understanding of code of pharmaceutical industry, the relevant regulatory and legimate knowledge (such as GCP, GPP, Copyright , Advertising and promotion law, confidentiality protection, et al), also the requirements on clinical practice and basic research such as declaration of Helsinki, animal ware fare.
• He/she must have a reputation for leading with high integrity, strong work ethics and compliant behavior
• Must understand and be able to plan, manage and execute budgets effectively.
• Collaborative, team oriented approach, as well as with key external stakeholders.  Experience being an active contributor to cross-functional teams and/or working in matrix organizations will be essential.  . 
• He/she will possess strong communication and presentation skills
• Works independently:  limited guidance/oversight. 
• Works broadly across functions to facilitate and support the affiliate’s medical and clinical activities as necessary.