Site ID Specialist (China-Beijing)
昆泰医药发展（上海）有限公司
- 公司规模：150-500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：2012-11-13
- 工作地点：北京
- 招聘人数：若干
- 工作经验：二年以上
- 学历要求：本科
- 职位类别：医药技术研发人员
职位描述
Description
RESPONSIBILITIES
Take independent responsibility for assigned site identification projects.
Assists Site ID lead on projects with increased protocol complexity, site numbers and/or customer SOPs or processes.
Utilizes historic site performance metrics, cluster sites, partner sites, feasibility data, and other data to identify potential sites.
Submits and reviews investigators for quality assurance status as applicable.
Tracks all project activities in Quintiles Database system.
Manages template documents for Confidential Disclosure Agreements (CDAs) and Site Interest Forms (SIFs).
Distributes tracks and negotiates the Confidential Disclosure Agreements (CDAs) with assistance from Management / QLegal as appropriate.
Designs, distributes, tracks and reviews Site Information Forms (SIFs) for completeness, site capability and availability.
Provides project progress reports to Internal and External project teams including department management.
Adheres to project timelines.
Contacts Feasibility, Medical Scientific Services and Clinical Operations leads to develop plan for identifying potential sites and processes for assigned projects.
Review and tier sites for contact based on historical site performance and other required criteria.
Enter new sites and investigators into the Quintiles Database, reviewing entries for duplicates.
Transfers applicable data and documentation to Clinical Operations.
Maintain departmental files, including site list and other project materials as required.
Responds to site questions about assigned studies in a timely manner.
Qualifications
REQUIRED KNOWLEDGE, SKILLS AND ABILITIES
Good Knowledge of medical terminology
Good interpersonal and organizational skills.
Proficient in the use of Microsoft Office.
Ability to work independently and effectively prioritize tasks.
Fluent in local language, spoken and written.
Ability to handle multiple tasks with varying deadlines.
Familiar with CRO's and the operation of Clinical Sites.
Must be highly motivated and organized.
Ability to maintain confidentiality.
Ability to establish and maintain effective working relationships with coworkers, managers and customers.
MINIMUM REQUIRED EDUCATION AND EXPERIENCE
Bachelors Degree in Health or Biological Science and 2 years' experience in a healthcare related field; or equivalent combination of education, training and experience.
RESPONSIBILITIES
Take independent responsibility for assigned site identification projects.
Assists Site ID lead on projects with increased protocol complexity, site numbers and/or customer SOPs or processes.
Utilizes historic site performance metrics, cluster sites, partner sites, feasibility data, and other data to identify potential sites.
Submits and reviews investigators for quality assurance status as applicable.
Tracks all project activities in Quintiles Database system.
Manages template documents for Confidential Disclosure Agreements (CDAs) and Site Interest Forms (SIFs).
Distributes tracks and negotiates the Confidential Disclosure Agreements (CDAs) with assistance from Management / QLegal as appropriate.
Designs, distributes, tracks and reviews Site Information Forms (SIFs) for completeness, site capability and availability.
Provides project progress reports to Internal and External project teams including department management.
Adheres to project timelines.
Contacts Feasibility, Medical Scientific Services and Clinical Operations leads to develop plan for identifying potential sites and processes for assigned projects.
Review and tier sites for contact based on historical site performance and other required criteria.
Enter new sites and investigators into the Quintiles Database, reviewing entries for duplicates.
Transfers applicable data and documentation to Clinical Operations.
Maintain departmental files, including site list and other project materials as required.
Responds to site questions about assigned studies in a timely manner.
Qualifications
REQUIRED KNOWLEDGE, SKILLS AND ABILITIES
Good Knowledge of medical terminology
Good interpersonal and organizational skills.
Proficient in the use of Microsoft Office.
Ability to work independently and effectively prioritize tasks.
Fluent in local language, spoken and written.
Ability to handle multiple tasks with varying deadlines.
Familiar with CRO's and the operation of Clinical Sites.
Must be highly motivated and organized.
Ability to maintain confidentiality.
Ability to establish and maintain effective working relationships with coworkers, managers and customers.
MINIMUM REQUIRED EDUCATION AND EXPERIENCE
Bachelors Degree in Health or Biological Science and 2 years' experience in a healthcare related field; or equivalent combination of education, training and experience.
公司介绍
ABOUT THE COMPANY
Quintiles Transnational Corp. strives unceasingly to exercise strong LEADERSHIP in our industry and to be the unquestioned FIRST CHOICE Contract Pharmaceutical Organization in an increasingly competitive marketplace.
We will DELIGHT our CUSTOMERS world-wide with the fullest range and highest quality of information and services, and with a spirit and a DEDICATION that bring professional esteem and admiration.
We demand the utmost level of EXCELLENCE, CREATIVITY, and SKILL from all our staff and management so that we add value to our customers by driving to PERFORMANCE goals in ways that are quantifiable.
We thrive on continuous IMPROVEMENT and QUALITY enhancements through attention to detail,consistent feedback, state-of-the-art systems, TRAINING and TEAMWORK.
We seek unendingly to bring our customers'PRODUCTS and SERVICES to MARKET ever sooner and to play a creative role in their achievement of earlier and greater commercial SUCCESS.
Throughout our commercial pursuits, we will respect and hold in esteemed honor our EMPLOYEES, to whom we owe our very existence.
We will maintain and enhance our reputation and integrity by demanding the highest possible ETHICAL STANDARDS and demonstrate by example an unyielding dedication to employees, customers, vendors, and shareholders. A SHARED VISION of success among these stakeholders will enhance the quality of life for all people of the world as we vigorously pursue our mission in an era of unprecedented OPPORTUNITY
Quintiles Transnational Corp. strives unceasingly to exercise strong LEADERSHIP in our industry and to be the unquestioned FIRST CHOICE Contract Pharmaceutical Organization in an increasingly competitive marketplace.
We will DELIGHT our CUSTOMERS world-wide with the fullest range and highest quality of information and services, and with a spirit and a DEDICATION that bring professional esteem and admiration.
We demand the utmost level of EXCELLENCE, CREATIVITY, and SKILL from all our staff and management so that we add value to our customers by driving to PERFORMANCE goals in ways that are quantifiable.
We thrive on continuous IMPROVEMENT and QUALITY enhancements through attention to detail,consistent feedback, state-of-the-art systems, TRAINING and TEAMWORK.
We seek unendingly to bring our customers'PRODUCTS and SERVICES to MARKET ever sooner and to play a creative role in their achievement of earlier and greater commercial SUCCESS.
Throughout our commercial pursuits, we will respect and hold in esteemed honor our EMPLOYEES, to whom we owe our very existence.
We will maintain and enhance our reputation and integrity by demanding the highest possible ETHICAL STANDARDS and demonstrate by example an unyielding dedication to employees, customers, vendors, and shareholders. A SHARED VISION of success among these stakeholders will enhance the quality of life for all people of the world as we vigorously pursue our mission in an era of unprecedented OPPORTUNITY