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无工作经验 -
招若干人 -
11-09 发布
职位描述
职位描述： One of the world’s largest CROs, PRA HealthSciences is transforming clinical trials through our people, innovation and operational transparency. Our 10,000+ employees operate in more than 80 countries, delivering a broad spectrum of clinical trial solutions that meet the demands of a diverse marketplace. It is our philosophy that the way in which we grow our business is to focus on our employees. As such, we recognize that successful careers are found within organizations that provide the support that employees need at work, the benefits they require outside the office as well as a good work / life balance.Main responsibilities:Field based KOL/Speaker Development1.Identification/ mapping of KOLs.2.Develop professional relationships with the targeting KOLs and build advocacy and gain contributions of KOL/decision-makers .3.Proactively Visit, Track, analyze and reports targeting KOLs advocacy, contribution and publication status in required system and KOL management tool as appropriate.4.Provide and discuss scientific information and data regarding new launched products to healthcare professionals to ensure quality and accuracy of key medical and scientific information on new treatment options by face to face visits speaker training and scientific communications.5.Scientific support of speaker training activities in the region with timely feedback.Information Management and Meeting/Events:1.May function as the Novartis medical speaker to present at Novartis/Society sponsored activities for up-to-date data based scientific and clinical information on Novartis product(s).2.Liaise and provide up-to-date medical support to facilitate listing of products in medical guidelines, RDL, formularies as appropriate.3.Participate in cross functional meetings as appropriate and sharing feedback of targeting KOLs advocacy and contribution.4.Prepare and tailor speaker slides in alignment with NP4 and Medical strategies.5.Manage unsolicited requests /objections comply with NP4 and China legal and regulatory requirements.Clinical Trials and Medical Affairs Studies1.Contribute to the identification and recommendation of appropriate KOL involvement and participation in Novartis sponsored clinical trials (PMS, Phase III and Phase IV studies) from assigned region.2.Conduct or Coordinate third party trials/animal studies/registry or epidemiology programs in assigned region and operation /follow-up the above program with Trial Master File to archive all relevant documents in align with Novartis SOPs.3.Evaluate requests to research fund as they pertain to Medical Affairs activitiesQualifications:Languages: Fluent in Chinese and English (oral and written)Experience/Professional requirement:1. Proven ability to develop and foster peer-to-peer, credible relationships in order to educate and influence KOL’s/decision makers.2. Working knowledge of the Healthcare System and of the clinical trial and research procedures as well as the ICH guidelines, GCP and other ethical guidelines relevant to the pharmaceutical industry.3. Thorough knowledge of clinical medicine, disease management, and medical research in at least one therapeutic area.4. Ability to synthesize recent scientific information ,analyze within strategic and regulatorysettings.5. Proven ability to use IT tools and interface effectively with a variety of technical platforms.6. Strong personal integrity, and customer focus.7. Excellent interpersonal communication, negotiation and advanced presentation skills.8. Effectively contribute to multifunctional teams.9. Must be able to adapt, organize, prioritize, and work effectively in a constantly changing field based environment. 职能类别： 医药学术推广
联系方式
北京市朝阳区建国路91号金地中心B座917
公司信息
RPS Inc. is a next generation global CRO, headquartered in the United States with the operations in 45 countries throughout Americas (US, Canada, Latin America), EMEA and Asia Pacific regions. RPS provides comprehensive global Phase 1-4 clinical development solutions to the pharmaceutical, biotechnology and medical device industries. By combining an experienced clinical research operations infrastructure with the industry’s largest resourcing engines, RPS is uniquely positioned to offer our Clients both integrated and full service global outsourcing solutions. These solutions are powered by highly experienced and seasoned study teams providing innovative, cost-effective and high quality services. RPS Asia Pacific Headquarters is located in Beijing, China and we have operations in 11 Countries in Asia Pacific region. With the rapid organic expansion of RPS in China & Asia Pacific, we are continuously looking for the experienced industry talents to join us. Our specialized staff of consultants is eager to discuss your career plans. Tell us about yourself experience, so the appropriate consultant can contact you. RPS is sensitive to your daily responsibilities. Tell us EXACTLY how to contact you and we will. For your convenience, you can also submit your resume. We look forward to discussing the opportunities and benefits of employment with RPS! For more information, please visit our website www.rpsweb.com.
