上海招聘

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.

IQVIA（纽交所代码：IQV）是全球专注生命科学领域的高阶分析、技术解决方案和临床研究服务供应商。IQVIA利用深入分析、前沿技术、大数据资源和广泛领域的专业知识，智能连接医疗生态的各个环节。IQVIA Connected Intelligence？快速敏锐地为客户提供强大的数据洞察，帮助客户加速创新医疗的临床开发和商业化进程，以更好的医疗成果惠及患者。IQVIA拥有约72,000名员工，足迹遍布100多个国家/地区。

IQVIA拥有多元化的加强型隐私技术和保障手段，能够在保护个人隐私的同时对信息进行管理和分析，帮助医疗利益相关方有效开展精准疗法，获得更佳的疗效。这些洞见和能力能够帮助生物科技、医疗器械、制药公司、医学研究者、政府机关、支付方以及其他医疗利益相关方，获得对疾病、人类行为和科技进步更深入的理解，共同朝着治愈各类疾病的方向迈进。