长沙招聘

1. Provide timely and high-quality medical input to business teams and achieve the following responsibilities:
1) Assist in business decision-making
l Provide medical inputs in new product planning and product strategic planning
l Sustain Medical expertise for the defined therapeutic areas, by self-studying and internal/external academic training
l Provide timely medical input in product crisis management
2) Participate in product commercial activity (Marketing, Sales)
l Provide medical input to product team in product positioning and differentiation
l Develop clinical research proposal for the defined therapeutic areas
l Review promotional materials and promotional activities
l Provide medical inputs in developing training program on disease knowledge in the defined therapeutic areas to sales training group
3) KOL management
l Regular communication with KOLs to share most updated medical information and maintain the relationship in the defined therapeutic areas
l Review the Investigator Initiated Study Program.
4) Lecture delivery and product training
l Regular lecture, to share most updated clinical trial data, interpreter treatment guideline and provide summary of product efficacy and safety profile.
l 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
l Provide medical input to medical information team in setting up medical query responding systems
l Liaise between business team and medical information team, to ensure timely delivery of medical information
l Proactively provide the latest medical information to internal and external customers on regular basis.
2) Regulatory activities
l Timely review and approve local product labeling for all products
l Provide medical input in feasibility studies for global trials
l Review and approval of phase IV clinical trial application based on Market needs
3) Clinical Studies

l Develop clinical trial protocol, reports and other documents according to GCP Guidelines/SFDA regulations/ and get HQ approval
l Identifies, evaluate and recommends potential investigators/sites on an on-going basis to assure placement of planned clinical studies with qualified investigators
l Responsible for the product trials/studies management according to GCP Guidelines/SFDA regulations

BACKGROUND REQUIREMENTS

l Medical Background in the defined therapeutic area, Master or Doctor Degree in therapeutic area is preferred.
l At least 2 years clinical practice
l At least 2 years medical affairs experience in multinational pharmaceutical companies
l Proficiency in both oral and written English
l Good capability of strategic and analytical thinking. Proactive planning and result oriented.
l Broad medical knowledge and good understanding about pharmaceutical business
l Good interpersonal communication skills

先声默沙东是由中美两家领先的医药公司——先声药业和默沙东联合打造的合资企业。2011年7月22日，默克公司和先声药业集团正式签署框架合作协议，先声默沙东应运而生。 随着中国经济的发展，大众生活方式的变化，以及人口老龄化进程的加快，高血压、糖尿病等慢性病发病率不断上升“十二五”期间中国将进一步加大医疗 卫生体制改革，更好的满足群众基本用药需求。基于造福患者的共同愿景，2011年7月，默克公司与先声药业在美国新泽西州罗韦（Rahway）签署战略合作协议，宣布在中国成立具有创新意义的盒子企业。合资企业总部设在上海。 我们的使命就是把适合中国患者的高质量、成熟的药品，覆盖到更广阔的地域，满足更多医疗需求，惠及更多中国大众。在合作初期，先声默沙东将重点关注心血管和代谢疾病两大领域，先声默沙东的多渠道营销平台在广度上覆盖更辽阔的区域，从东部的沿海到内陆，从发达城市到医疗咨询稀缺的农村；在深度上生渗透到更基层的就医点，从三级医院懂啊社区卫生中心，乡镇卫生院，满足更多人群的医疗需求。 先声默沙东根植于两家公司身后的企业文化和共同的价值观。