医学顾问-Medical Advisor
杭州默沙东制药有限公司
- 公司规模:150-500人
- 公司性质:外资(欧美)
- 公司行业:制药/生物工程
职位信息
- 发布日期:2013-03-26
- 工作地点:北京
- 招聘人数:若干
- 工作经验:二年以上
- 学历要求:硕士
- 语言要求:英语熟练
- 职位类别:生物工程/生物制药
职位描述
Job description - Medical Advisor
Position: Medical Advisor
Report to: Medical Affairs Manager
JOB SUMMARY
The Medical Advisor provides a bridge between clinical research and the marketing and sales department as well as the remaining departments within the organization. He/she specifically provides an authoritative opinion and answers medically based questions concerning medical, legal and regulatory matters enabling colleagues to comply with the relevant statutory requirements.
? In charge of the defined therapeutic area and is taking the overall responsibility to medical input support the business teams.
? Responsible for pro-actively involving 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
KEY RESULT AREAS & JOB ACTIVITIES /TASKS
1. Provide timely and high-quality medical input to business teams and achieve the following responsibilities:
1) Assist in business decision-making
? Provide medical inputs in new product planning and product strategic planning
? Sustain Medical expertise for the defined therapeutic areas, by self-studying and internal/external academic training
? Provide timely medical input in product crisis management
2) Participate in product commercial activity (Marketing, Sales)
? Provide medical input to product team in product positioning and differentiation
? Develop clinical research proposal for the defined therapeutic areas
? Review promotional materials and promotional activities
? Provide medical inputs in developing training program on disease knowledge in the defined therapeutic areas to sales training group
3) KOL management
? Regular communication with KOLs to share most updated medical information and maintain the relationship in the defined therapeutic areas
? Review the Investigator Initiated Study Program.
4) 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,
2. Provide timely and high-quality medical input to medical teams and achieve the following responsibilities:
1) Medical information Support
? 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
? Proactively provide the latest medical information to internal and external customers on regular basis.
2) Regulatory activities
? Timely review and approve local product labeling for all products
? Provide medical input in feasibility studies for global trials
? Review and approval of phase IV clinical trial application based on Market needs
3) Clinical Studies
? Develop clinical trial protocol, reports and other documents according to GCP Guidelines/SFDA regulations/ and get HQ approval
? Identifies, evaluate and recommends potential investigators/sites on an on-going basis to assure placement of planned clinical studies with qualified investigators
? Responsible for the product trials/studies management according to GCP Guidelines/SFDA regulations
BACKGROUND REQUIREMENTS
? Medical Background in the defined therapeutic area, Master or Doctor Degree in therapeutic area is preferred.
? At least 2 years clinical practice
? At least 2 years medical affairs experience in multinational pharmaceutical companies
? Proficiency in both oral and written English
? Good capability of strategic and analytical thinking. Proactive planning and result oriented.
? Broad medical knowledge and good understanding about pharmaceutical business
? Good interpersonal communication skills
Position: Medical Advisor
Report to: Medical Affairs Manager
JOB SUMMARY
The Medical Advisor provides a bridge between clinical research and the marketing and sales department as well as the remaining departments within the organization. He/she specifically provides an authoritative opinion and answers medically based questions concerning medical, legal and regulatory matters enabling colleagues to comply with the relevant statutory requirements.
? In charge of the defined therapeutic area and is taking the overall responsibility to medical input support the business teams.
? Responsible for pro-actively involving 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
KEY RESULT AREAS & JOB ACTIVITIES /TASKS
1. Provide timely and high-quality medical input to business teams and achieve the following responsibilities:
1) Assist in business decision-making
? Provide medical inputs in new product planning and product strategic planning
? Sustain Medical expertise for the defined therapeutic areas, by self-studying and internal/external academic training
? Provide timely medical input in product crisis management
2) Participate in product commercial activity (Marketing, Sales)
? Provide medical input to product team in product positioning and differentiation
? Develop clinical research proposal for the defined therapeutic areas
? Review promotional materials and promotional activities
? Provide medical inputs in developing training program on disease knowledge in the defined therapeutic areas to sales training group
3) KOL management
? Regular communication with KOLs to share most updated medical information and maintain the relationship in the defined therapeutic areas
? Review the Investigator Initiated Study Program.
4) 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,
2. Provide timely and high-quality medical input to medical teams and achieve the following responsibilities:
1) Medical information Support
? 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
? Proactively provide the latest medical information to internal and external customers on regular basis.
2) Regulatory activities
? Timely review and approve local product labeling for all products
? Provide medical input in feasibility studies for global trials
? Review and approval of phase IV clinical trial application based on Market needs
3) Clinical Studies
? Develop clinical trial protocol, reports and other documents according to GCP Guidelines/SFDA regulations/ and get HQ approval
? Identifies, evaluate and recommends potential investigators/sites on an on-going basis to assure placement of planned clinical studies with qualified investigators
? Responsible for the product trials/studies management according to GCP Guidelines/SFDA regulations
BACKGROUND REQUIREMENTS
? Medical Background in the defined therapeutic area, Master or Doctor Degree in therapeutic area is preferred.
? At least 2 years clinical practice
? At least 2 years medical affairs experience in multinational pharmaceutical companies
? Proficiency in both oral and written English
? Good capability of strategic and analytical thinking. Proactive planning and result oriented.
? Broad medical knowledge and good understanding about pharmaceutical business
? Good interpersonal communication skills
公司介绍
我们坚信患者为先;
我们的事业是保护人类健康,提高生活质量;
我们汇集优秀人才,并相信承诺予人,发展之本。
这是默沙东作为世界制药企业领先者的承诺和使命。
默沙东(在美国名为默克公司),作为全球500强企业多次获得赞誉,包括16次获得美国《财富》杂志“美国十大最受推崇公司”称号。自1992年进入中国以来,我们致力于通过专业的学术交流,为医生提供具有价值的产品和治疗领域信息,从而使默沙东的药品更好地造福于患者。
中国已成为默沙东全球发展战略的重要部分。默沙东正在中国积极把握机遇,拓展业务,实现自身的飞跃式发展。
默沙东坚信所有的成功最终取决于优秀的人才。我们知人善任,并人尽其才。如果您和我们一样追求卓越并分享同一信念,现在就加入默沙东中国!
我们的事业是保护人类健康,提高生活质量;
我们汇集优秀人才,并相信承诺予人,发展之本。
这是默沙东作为世界制药企业领先者的承诺和使命。
默沙东(在美国名为默克公司),作为全球500强企业多次获得赞誉,包括16次获得美国《财富》杂志“美国十大最受推崇公司”称号。自1992年进入中国以来,我们致力于通过专业的学术交流,为医生提供具有价值的产品和治疗领域信息,从而使默沙东的药品更好地造福于患者。
中国已成为默沙东全球发展战略的重要部分。默沙东正在中国积极把握机遇,拓展业务,实现自身的飞跃式发展。
默沙东坚信所有的成功最终取决于优秀的人才。我们知人善任,并人尽其才。如果您和我们一样追求卓越并分享同一信念,现在就加入默沙东中国!
联系方式
- 公司地址:下沙经济开发区文海北路199号