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臨床監(jiān)查員

1萬-2萬
  • 廣州天河區(qū)
  • 1-3年
  • 本科
  • 全職
  • 招2人

職位描述

藥品臨床監(jiān)查Ⅱ期Ⅲ期
Position overview:
Working as an Clinical Research Associate is ultimately responsible for the successful management of investigator sites throughout the
trial lifecycle. Key responsibilities include:
? Full ownership of investigator sites for assigned studies with responsibility for the successful management of the site right through to close-out.
? Planning and conducting various site visits (feasibility, site selection, interim and close-out) in accordance with the clinical monitoring plan.
? Developing effective relationships with investigator site staff to ensure that key clinical metrics are met.
? 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.
? Ensuring integrity of clinical data through an ability to sufficiently maintain site tracking records and work diligently to relevant guidelines

You will receive the support you need to develop personally and professionally and work in an environment where you matter. Our team pushes forward together.
United in solving problems, developing close site relationships and reaching the end goal. Operating as a key part of a global study team, the CRA plays a fundamental role in our clients’ drug development processes.

You are:

Dedicated, collaborative and inspire others.
Here we want our employees to succeed and ensure that they are set up for this success through constant training, development and support. To enable success in this position you will have:
? Prior experience of working in investigator site management, including conducting monitoring visits, from either a pharmaceutical company or a CRO environment.
? A working knowledge of ICH-GCP guidelines and local and international regulatory requirements is essential.
? You will be educated to degree level, have equivalent experience or be a licensed healthcare professional.

職位福利：五險一金、帶薪年假、補充醫(yī)療保險、餐補、交通補助、年底雙薪、通訊補助

職位亮點：global項目,腫瘤

工作地點

珠江新城

職位發(fā)布者

張睞/人事經(jīng)理

昨日活躍
立即溝通
公司Logo愛恩康臨床醫(yī)學(xué)研究(北京)有限公司
At ICON we believe that our people are the most important asset. It is they who have helped to make ICON the success it is. Their commitment to clients, quality and delivery has earned ICON its enviable reputation. About DOCS: DOCS- ICON Resourcing Solutions is a division of ICON plc that provides global staffing solutions to Pharmaceutical, Biotechnology, Medical Device companies and CROs in over 39 countries. We can recruit in virtually any location having access to offices in over 25 countries. This truly makes DOCS a company with global reach and personal focus. ICON has been in APAC since 1996 and the DOCS division of ICON is now expanding in the APAC region. Our Services: We are a specialist recruitment division focusing in Clinical Research, Medical Affairs, Regulatory Affairs, Drug Safety, Health Economics, Data Management& Statistics, Quality Assurance etc. Our full-spectrum resourcing solutions extend from contingent staffing, to functional resourcing, large-scale FSP and executive search. In addition, DOCS has developed a tailored training division‘CRAcademy’ to provide Traineeships and Training. We can recruit in virtually any location having access to offices in over 25 countries. This truly makes DOCS a company with global reach and personal focus. Our History: DOCS was formed in The Netherlands in 1997 and grew to become the premier resourcing provider to the European pharmaceutical industry. The company was acquired by ICON plc in 2007 and was merged with ICON’s existing resourcing division, ICON Contracting Solutions. The merged company is now known as DOCS, and offers clients over 15 years of experience in the provision of global resourcing solutions. For more information, please visit www.docsglobal.com& www.iconplc.com.
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