长沙 [切换城市] 长沙招聘长沙生物/制药/医疗器械招聘长沙生物工程/生物制药招聘

Feasibility Specialist

昆泰企业管理(上海)有限公司

  • 公司规模:500-1000人
  • 公司性质:外资(欧美)
  • 公司行业:制药/生物工程

职位信息

  • 发布日期:2019-06-03
  • 工作地点:上海-徐汇区
  • 招聘人数:1人
  • 工作经验:3-4年经验
  • 学历要求:本科
  • 职位月薪:1-1.7万/月
  • 职位类别:临床研究员

职位描述


  

PURPOSE

  

Perform, manage and co-ordinate activities associated with feasibility for assigned opportunities/ projects. Collate data and present to internal stakeholders together with recommendations. Train and mentor junior staff.

  

 

  

RESPONSIBILITIES

  

? Accountable for making recommendations for Quintiles commitments for future studies in terms of recruitment rate,

  

timelines and screen failure rates

  

? Take independent responsibility for capability exercises and larger feasibility projects / deliverables

  

? Prepare for strategy calls by research into therapeutic areas using internal databases, scientific literature, the internet and expert medical knowledge to provide background information.

  

? Attend strategy calls with internal stakeholders including Medical Directors and Advisors, Business Developers, Sales Staff and Program Directors. Present background information, particularly including country recruitment and screen failure data.

  

? Design of protocol-specific questionnaires for collection of global feasibility information for individual countries and sites in order to determine patient populations and protocol suitability.

  

? Develop feasibility analysis systems and data collection tools in Excel to support the collection of associated metrics

  

? Provide appropriate tools for country feasibility leads to carry out feasibility and capability exercises e.g. telephone training and detailed emails

  

? Coordinate the collection and analysis of global feasibility information to meet the challenging timelines of the proposal process and independent feasibility assessments

  

? Reconcile and interpret feasibility data, providing solid recommendations to internal stakeholders

  

? Production of feasibility text for proposals and feasibility reports

  

? Review budgets for stand-alone paid feasibility studies

  

? Train and support new team members

  

? Attend client meetings as required to present feasibility process and explain recommendations

  

? Liaise with internal and external customers globally to coordinate the collection and delivery of feasibility data.

  

? Maintain and update departmental information repositories and databases

  

? Undertake therapeutic training, as necessary, and keep abreast of developments in clinical research generally

  

All responsibilities are essential job functions unless noted as nonessential (N).

  

 

  

REQUIRED KNOWLEDGE, SKILLS AND ABILITIES

  

? Clinical/project management experience is preferred.

  

? General knowledge and understanding of company clinical systems, procedures and corporate standards.

  

? Good knowledge of medical terminology, GCP, FDA regulations, and Drug Development process.

  

? In-depth understanding of clinical research.

  

? Excellent communication, organizational and interpersonal skills.

  

? Fluid report writing in English

  

? Strong computer literacy, including well-developed computer skills in applicable software.

  

? Ability to work independently and effectively prioritize tasks.

  


MINIMUM REQUIRED EDUCATION AND EXPERIENCE

  

? Bachelor’s Degree in Healthcare or Biological Science and a minimum of 3 years related experience in clinical research; or equivalent combination of education, training and experience

  

 

  

PHYSICAL REQUIREMENTS

  

? Extensive use of keyboard requiring repetitive motion of fingers.

  

? Extensive use of telephone and face-to-face communication requiring accurate perception of speech.

  

? Regular sitting for extended periods of time.

  

? May require occasional travel.

  


职能类别: 临床研究员

关键字: CRA经验 英语好

公司介绍

QuintilesIMS pioneered the idea of helping pharma companies conduct objective clinical trials to establish not only whether a drug is effective, but who can take it safely. Our customers have relied on us to design and conduct rigorous clinical research for decades, from small studies to multinational mega-trials. However, we continue to develop new ways of interpreting and evaluating data that allow us to create more effective trials and determine outcomes faster.
 
If that is your passion, we have a place for you.

联系方式

  • Email:chinacampus@iqvia.com
  • 公司地址:地址:span建国门外大街光华东里8号中海广场