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无工作经验 -
本科 -
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:?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.Qualifications:?Tertiary qualification; life science, medical, paramedical, pharmaceutical related degree?Minimum 1 year monitoring experience. Preference is given to candidates with at least 2 years of global trial experience, working for global pharmaceutical company or global CRO?Demonstrated strong understanding of company’s systems and processes?Demonstrated proficiency in the monitoring and management of clinical trialsTeam orientated personality with high degree of flexibility 职能类别： 临床研究员
联系方式
武汉
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.
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