• 无工作经验
  • 本科
  • 招若干人
  • 02-22 发布
  • 五险一金
  • 补充医疗保险
  • 补充公积金
  • 免费班车
  • 交通补贴
  • 弹性工作
  • 定期体检

职位描述

Job Summary:Independently performs activities related to Project management process by coordinating activities for routine studies in compliance with appropriate protocol, Standard Operating Procedures (SOPs) and regulatory agency guidelines, in a timely, efficient, and quality manner.Essential Job Duties:Independently drafts protocols, sample analysis outlines (SAOs), amendments and study schedules with some oversight, using proposal outline or client-supplied information.Responsible for report preparation, including table and figure preparation. Compiles analytical information from laboratory groups.Responsible for data table compilation including quality review oversight and data table transfer.Communicates and interacts with study team, other departments and clients as applicable.Serve as the primary contact in communication and interaction with other departments and clients as applicable.Proven ability to plan, prioritize and manage workload and multiple responsibilities.Demonstrated ability to independently use project tracking systems as appropriate.Maintains well documented, organized and up-to-date study files including study schedule, protocol and correspondence as applicable.Assists SD/PI in monitoring study progress.Serves as a backup PI/SD on project management tasksSchedules study phases in coordination with SD/PI and lab operations.Proven ability to participate in and assist Study Director/Principal Investigators with pre-initiation and other study related meetings as required.Proven ability to manage increasingly complex projects and study designs and/or increased study load.Demonstrated capability to manage work for key clients.Demonstrated ability to support and be involved in process improvement initiates and endeavorsReviews QAU report audits. Submits audit responses for approval as appropriate. Follows up with appropriate personnel to ensure that all necessary report/raw data clarifications are completed within specified timelines. Assists with routine client visits as requested.Performs other related duties as assignedAssists in setting up and performing method development and validation of various analytes in a variety of matrices.Performs complex analyses using unfamiliar or new methods, asking for scientific guidance as needed.Makes suggestions for modifications in test methods or proceduresEducation/QualificationBS/BA degree in science plus at least 4-5 years experience or MS degree with 2-4 years experience.?Efficient use of word processing software, database, spreadsheet, and specialized software.?Proficient in concise writing. Writing should require little or no external review or edit.?Adherence to grammar, punctuation, composition, and spelling according to company standard conventions.?Experience on a variety of studies performed in the department and exposure to a diverse client base.?Knowledge of regulatory agency guidelines.Experiences:Two years of study coordinator for large molecule or related experience.?Excellent communication, presentation, and interpersonal skills.?Excellent attention to detail.?Efficient in prioritizing and managing time. 职能类别: 生物工程/生物制药 关键字: 项目协调 大分子 生物分析

联系方式

周浦康新公路3377号

公司信息

Why Covance? At Covance, you will join like-minded professionals who, together, build our reputation as one of the world's largest and most respected contract research organizations. In choosing Covance, you will be part of a dedicated team that makes a difference in helping to deliver life-saving and life-enhancing medicines to people around the world. We Offer Covance’s ongoing success offers team members unsurpassed growth and career development opportunities. At Covance, we help make the miracles of medicine a reality. We offer opportunities to work on diverse, challenging projects with bright, interesting colleagues while building a flexible and rewarding career. There is no better time to join us!

猎才二维码