莆田招聘

Business Segment

Healthcare Quality

About Us

At GE China, we are imagination at work. From our Aviation Systems facilities in Suzhou where we manufacture state-of-the–art aerostructures to our Healthcare CT, MRI and X-Ray facilities in Beijing, the GE China teams are dedicated to turning imaginative ideas into leading products and services that solve some of the world’s toughest challenges. Join an innovative industry leader for an unprecedented career of significant influence within the region and beyond. Here you’ll find the professional freedom and flexibility to create your own career path combined with the enduring strength of a proven global company. Work alongside the best minds in the business and take advantage of GE’s generous investment in your education, growth and advancement. If you’re interested in working with true leaders in a goal-oriented environment driven by best-in-class processes, this is the career for you. Become a part of a company internationally known for its reputation as an industry leader, dynamic culture and unlimited opportunity to succeed locally and globally. Join GE in creating the next generation of products and services that will impact the world for generations to come.

Role Summary/Purpose

GE is an equal opportunity employer, offering a great work environment, challenging career opportunities, professional training and competitive compensation.The Clinical Research Associate (CRA) supports the Business Research Managers (RMs) through monitoring and coordinating of clinical research studies to ensure research is compliant with Good Clinical Practices and other applicable regulations and company procedures.

Essential Responsibilities

• Supports RMs in performing initial contact and participates in the assessment and selection of qualified investigators for inclusion in research. • Supports RMs in completing Pre-Selection, Initiation, Monitoring, and Closeout site visits, or coordinate contractors in their performance of these activities as needed. Tracks required documentation from study site. • Reviews and approves study documentation such as protocols, informed consents, amendments, case report forms, and study reports. • Supports RMs with initiation of research and site training. • Ensures compliant recording and reporting of any adverse events occurring during research. • Interfaces with Regulatory Agencies as required. • Ensures overall regulatory compliance of investigational sites with applicable regulations. • Reviews clinical history file for completeness throughout research process. • Assists with the coordination and conducting of the Research Review meetings.

Qualifications/Requirements

1. Bachelor’s degree (or internationally recognized equivalent) in a science related field or R.N. with a minimum of 5 years experience with clinical applications, research management or regulatory affairs within the pharmaceutical or medical device industry OR minimum of 9 years progressive experience with clinical applications, research management or regulatory affairs within the pharmaceutical or medical device industry.2. Strong experience of all aspects of the clinical research process, including site selection, investigator qualifications, monitoring, protocol and report writing.3. Excellent verbal and written communication and presentation skills with the ability to communicate business issues in English in an easy to understand manner4. Strong problem solving, influencing and negotiation skills; diplomatic team player5. Ability to travel up to 20% of time for responsibilities focused on research management and up to 75% for responsibilities focused on research site monitoring.

Desired Characteristics

1. Demonstrated project management skills to prioritize, plan, delegate & evaluate deliverables; well organized and structured, attention to detail.2. Prior medical device experience.3. Experience interfacing with Regulatory Agencies such as FDA.4. Experience with Global research regulations.5. Auditing experience.6. Clinical trial professional certification, e.g. CCRP, CCRA or CCRN

通用电气（GE) 公司是一家全球领先的科技、服务和金融公司，是全球最大的多元化企业，致力于解决世界上最棘手的问题。GE的产品和服务范围广阔，从能源、石油天然气、水处理、航空、医疗、运输系统、家电、照明，到金融，客户遍及全球100多个国家，拥有30多万员工。杰夫?伊梅尔特先生是现任董事长及首席执行官。

GE公司的历史可追溯到托马斯?爱迪生，他于1878年创立了爱迪生电灯公司。1892年，爱迪生通用电气公司和汤姆森－休斯顿电气公司合并，成立了通用电气公司（GE）。GE是道 琼斯工业指数1896年设立以来唯一至今仍在指数榜上的公司。

2011年GE的年销售达1420亿美元。

GE现有6个产业部门，其中包括：航空、交通运输、医疗、能源、GE金融、家庭和商业解决方案。

GE (NYSE: GE) is Imagination at Work – an advanced global technology, service and finance company that is taking on the world’s toughest challenge. Widely recognized as the world’s largest multi-business company, GE excels in a variety of sectors including energy, oil and gas, water treatment, aviation, healthcare, transportation, lighting, appliances and finance. GE serves customers in more than 100 countries and employs more than 300,000 people worldwide. Jeffrey R. Immelt is Chairman of the Board and Chief Executive Officer of GE.

The company traces its beginnings to Thomas A. Edison, who established Edison Electric Light Company in 1878. In 1892, a merger of Edison General Electric Company and Thomson-Houston Electric Company created General Electric Company. GE is the only company listed in the Dow Jones Industrial Index today that was also included in the original index in 1896.

Total revenue of GE reached $142.0 billion in 2011.

GE is having six businesses including: Aviation, Transportation, Healthcare, Energy, GE Capital, Home and Business Solutions.