北京相关职位: 院外销售经理 新药研究部立项调研主管/经理 营销专员/助理(无责底薪5000+高提成+月薪过万) 制剂实验员 生化诊断试剂研发员 医疗器械注册及政策法规专员 系统维护员 生信工程师 Bioinformatics Engineer 注册专员 医疗器械销售经理(骨科产品、待遇优厚)
周边城市招聘: 上海 浙江 安徽 广东 山东 河北 重庆 北京 江苏 湖南
企业入驻日期: 2017-11-09
职位描述: Duties and Responsibilities (including but not limited to):Working fully as part of our Core Team and based at the PRA offices, the Clinical Research Associate is ultimately responsible for the successful management of investigator sites throughout the site lifecycle, whilst working in accordance with ICH-GCP guidelines, the study protocol, applicable local and international regulatory requirements and internal Standard Operating Procedures.With full ownership of investigator sites for your assigned studies, your involvement begins at site feasibility stage, with responsibility for the successful management of the site right through to close-out. In addition to planning and conducting various site visits (feasibility, site selection, interim and close-out) in accordance with the clinical monitoring plan, you will foster effective relationships with investigator site staff to ensure that key clinical metrics are met. This will involve establishing innovative ways of increasing site and patient recruitment. When issues do occur, the Clinical Research Associate proactively and promptly implements corrective action plans, and, when applicable, escalates issues to more senior members of the study team. You may also design and deliver training to site staff, when appropriate.Typical duties will likely include preparing for and attending investigator meetings, coordinating the timely shipment and the subsequent proper storage and accountability of clinical supplies and following-up of drug safety issues that have occurred at your site. You will ensure the integrity of clinical data through your ability to sufficiently maintain site tracking records and work diligently to relevant guidelines.Through your ability to operate as a key part of a global study team, you will play a fundamental role in our client’s drug development process.Education and Work Experience:The successful candidate for this role will be able to demonstrate prior experience of working in investigator site management, including conducting monitoring visits, from either a pharmaceutical company or a CRO environment.Ideally we would like for you to have at least 1 year of monitoring experience.It is essential that you have prior working knowledge of ICH-GCP guidelines and local and international regulatory requirements.Fluency in English is an absolute requirement, as well as an ability to communicate effectively with others and manage your time effectively. 职能类别: 临床协调员
北京市朝阳区建国路91号金地中心B座917
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.
产品注册 0.8-1万/月
中药炮制研究员 5-7千/月
销售顾问(无责底薪5000+高提成+月薪过万) 1-1.5万/月
医学检验室主任 2-4万/月
生产技术人员/灭菌员/生物医学工程(BJTK0132) 4-6千/月
注册专员 3-4千/月
销售经理 0.5-1.5万/月
毒理学研究员 0.6-1万/月
中药方剂研究员 0.8-1万/月
设备操作工 3-4.5千/月
高级临床监查员 0.8-1万/月
临床协调员/CRC/临床试验/临床研究员/研究护士/SMO 4.5-6千/月
临床协调员CRC-I期 4-8千/月
北京相关职位: 院外销售经理 新药研究部立项调研主管/经理 营销专员/助理(无责底薪5000+高提成+月薪过万) 制剂实验员 生化诊断试剂研发员 医疗器械注册及政策法规专员 系统维护员 生信工程师 Bioinformatics Engineer 注册专员 医疗器械销售经理(骨科产品、待遇优厚)
周边城市招聘: 上海 浙江 安徽 广东 山东 河北 重庆 北京 江苏 湖南
企业入驻日期: 2017-11-09