[北京]辉瑞制药2010海外留学生校园招聘-医学顾问

 

辉瑞制药公司校园招聘医学顾问

 

公司简介：

辉瑞是全球领先、历史悠久、以研发为基础的跨国制药企业。我们无与伦比的产品覆盖广泛的治疗领域，改善了世界各地患者的生活质量，使人类生活得更长寿、更健康和更有活力。公司倡导"领导人才，团队精神，革新创造，客户至上，力争上游，社区精神，尊重他人，道德观念，追求品质"九大核心价值观，在全球获得广泛认可和赞誉。

 

在中国，辉瑞公司恪守"健康世界，辉瑞使命"的承诺，业务快速发展，在行业内一直保持领先地位，并有雄心勃勃的长期发展计划。人才是公司发展的基础，辉瑞公司始终将人才发展战略与业务发展战略并重。在2007年、2008年壮志凌云进行的招聘计划中，我们在全国范围内共招募了上千名高素质的医学信息沟通专员。在经历了系统的培训后，新专员已经成为一支充满活力的生力军，为公司的发展做出了巨大贡献并与公司共同成长。

 

现在，公司众多新产品上市在即，销售区域持续扩张，新的机遇再次出现！如果你有信念，有热情，有对成功的渴望，有迎接真正挑战的决心，有不断学习的意愿，那么请你来加入我们吧，我们将帮助你成功！

 

加入辉瑞公司，一起为建设美好健康新世界而努力！

 

Position: Medical Advisor

Working Location: Beijing

 

JOB SUMMARY

- Medical Advisor is the medical professional who is required to be pro-actively involved in all aspects of a product's life cycle, from pre-launch to subsequent promotion, through marketing and sales, by providing medical input to enhance the product's value in all areas of business.

- Medical Advisor is required to support business decision-making in China by providing medical and technical inputs for the defined therapeutic areas under supervision.

- Medical Advisor is the medical professional representing Pfizer in communicating with KOLs and academia for the defined therapeutic areas under supervision.

As such, good understanding and comprehensive knowledge of the defined therapeutic area, proactive attitude and professional behavior are mandatory.

 

KEY RESULT AREAS & JOB ACTIVITIES /TASKS

1.Medical Input in Product Commercial Activity (Marketing, HCBT, Sales)

- Provide medical input to product team in product positioning and differentiation

- Develop publication plan and clinical research proposal for the defined therapeutic areas

- Review and approval promotional materials and promotional activities

- Provide medical inputs in developing training program on disease knowledge in the defined therapeutic areas to sales training group

- Participating National Sales Conferences (POAs) and helping resolve medical issues on products and therapeutic areas

2.Medical Input to Business Decision-Making Under Supervision

- Provide medical inputs in new product planning and product strategic planning under supervision.

- Sustain Medical expertise for the defined therapeutic areas, by self-studying and internal/external academic training

- Provide timely medical input in product crisis management under supervision.

3.Medical Product Life Cycle Management Under Supervision

- Develop and implement medical effective medical strategy to leverage product development.

- Develop publication plan for the defined therapeutic areas to support in-line products development

- Design research direction & proposals, and implement it as required with good quality and speed.

- Provide IIR review and manage it with good documentation quality

- Contributes to publication of clinical data.

4.KOL Management Under Supervision

- Set up and update KOL database for the defined therapeutic areas

- Regular communication with KOLs to share most updated medical information in the defined therapeutic areas under supervision

- Facilitate KOL in publishing articles in top national or international academic journals and national conference in the defined therapeutic areas

5.Cooperation with Local Medical Association or CDC

- Provide necessary input from product and therapeutic perspective, to assist collaboration programs with local Medical associations, CDC, and other academic or government agencies

- Assist dedicated Medical Advisor in review and approval of Investigator Initiated Research applications.

6.Lecture Delivery and Product Training

- Regular lecture, to share most updated clinical trial data, interpreter treatment guideline and provide summary of product efficacy and safety profile.

- Product training to internal and external customers, including LT, sales and KOLs.

7. Medical Information

- Provide medical input to medical information team in setting up medical query responding systems

- Liaise between business team and medical information team, to ensure timely delivery of medical information

- Provide timely responses to both internal and external customers' queries on the information of Pfizer' s in-market and pre-launched products and relating therapeutic areas

- Provide medical input to Safety Officer in handling Pfizer's product safety information

- Proactively provide the latest medical information to internal and external customers on regular basis.

8. Medical Input in Drug Registration Activities

- Timely review and approve local product labeling for all Pfizer products under supervision

- Provide medical input in feasibility studies for global trials.

- Develop phase IV clinical trial application based on Market needs.

- Officially input on study site selection from commercial prospective

- Join protocol synopsis and study report discussion/finalization meeting, to get the first hand information about local new product clinical development

 

BACKGROUND REQUIREMENTS

1. Educational /Training

Medical Background, Post graduate Degree in cardiovascular and/or metabolic disease preferred

2. Working Experiences

- 1 years clinical practice or medical affairs experience in other multinational pharmaceutical companies

- Experience in designing and executing Clinical Research would be a plus

- Good medical knowledge for the defined therapeutic area

- Adequate understanding about pharmaceutical business

- Proficiency in English and good computer usage

 

COMPETENCIES REQUIREMENTS

1. Ability Functional

- Strong and continuous learning capability and adaptability

- Good interpersonal communication skills

- Careful working attitude

- Customer focus

- Excellent Teamwork/Collaboration

2. Cultural Competencies (Leader Behaviors)

- Sustain Focus on Performance

- Align Across Pfizer

- Create an Inclusive Environment

- Manage Change

- Develop People

 

有意者请将中英文简历发送到：hr@

截止日期：2010年7月20日

 

注意：

1、邮件标题格式：XXX学校＋姓名＋专业＋学历＋毕业时间＋应聘医学顾问

2、此职位针对硕士或者博士，如果是本科或者大专生请勿投递简历

谢谢！

 

2010年7月