Within the framework of Group SOP and China regulation, develop strong medical strategy and design solid and/or innovative medical activities to align with brand strategy, meet China unmet medical practice need, and well manage the product life cycle.
Main responsibilities / job expectations:
- Develop medical strategy and activities by close collaboration with BU, HQ and VA
- For clinical trial project, guarantee the scientific, ethic, quality could meet the highest requirements of Group and NMPA
- For non-clinical trial project, guarantee the progress and quality in relevant therapeutic area can meet the requirements of BU, compliance with TA practice and trend
- To collect and analyze the medical information, ensure professional & accurate evaluation of the local medical practice, the treatment guidelines, published literature and develop the scientific link to ensure the early integration into the projects in China
- Promotion material reviewing and approving, non-promotional material developing and reviewing
- Support MR training, including training material development, special training activities conduction
- Ensure professional organization of advocacy support according to local regulations on all levels such as Thought Leader interaction, Advisory Board set-up
Knowledge, abilities & experience:
- Ideal: PH.D in clinical medicine
- Minimum: Master degree major in clinical medicine
- 1- 2 years clinical experience in related therapeutic area
- 1-2 years MA experience or related TA senior MSL experience in multi-national pharmaceutical
- Strong business acumen and strategic thinking
- Excellent written and oral English
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