南京招聘

职位描述：
Perform analysis and processing of medical imaging data for clinical trials in compliance with study protocols and applicable regulatory agencies. Issue and resolve queries with investigator sites and academic centers to ensure follow-up on imaging-related issues. Validate and maintain a database of medical imaging data and associated results.
Perform quality assurance checks on radiographic and photographic medical imaging data to ensure protocol specific requirements are met
？ Perform established image processing techniques (converting imaging formats, performing preliminary measurements of lesions and volumes) across multiple modalities (including but not limited to CT, MRI, Ultrasound) using proprietary software as well as other third party software
？ Perform DXA Image processing, Longitudinal Instrument Quality Control, and Cross Calibration tasks.
？ Perform image processing and measurements on Ophthalmic imaging; Identify quality issues (including poor image acquisition, artifacts, opacities, and other medical/surgical conditions) and work with Investigator Sites to rescan patient images and/or correct imaging techniques
？ Perform project specific tasks in compliance with Good Clinical Practices (GCP), regulatory requirements (21CFR Part 11), applicable departmental and companywide SOPs, and project specific protocols
？ Act as liaison with investigator site personnel to resolve issues that arise over the course of the clinical trial.
？ Ability to prioritize and manage time sensitive tasks for multiple projects
？ Mentor and assist in training of internal personnel
？ Perform other duties as required by the position


Job Qualifications :
 
Minimum 1-3 years of experience in clinical research or imaging related field or equivalent skills preferred.
？ Proficient in the English language
Bachelor’s Degree in Health Sciences or equivalent medical imaging related work experience required 举报 分享

精鼎医药（Parexel International）是全球领先的药物研究合同委托机构（CRO），总部位于美国生物医药圣地马萨诸塞州的波士顿附近，在世界各地拥有71个办事处，约17,600 名员工，为超过100个国家的客户提供服务。

精鼎医药成立于1982年，在三十多年的历程中，一直致力于发展成为全球生物制药和医疗器械行业首屈一指的新型医学疗法开发和商业化服务供应商，并且取得了卓越成果。目前，我们能够提供全世界CRO领域全面的新药临床阶段研发服务，服务内容包括新药开发策略的拟定与计划、国际临床试验规划执行及整合、临床试验的监测、临床试验数据处理、临床研究统计分析、临床试验总结及统计报告、临床试验稽核服务、临床试验供应和物流服务、临床电子数据采集、临床医学信息管理系统、新药查验登记事务和国际临床试验相关法规咨询等。

将我们的全球法规监管专业经验、I-IV期临床研究服务、整合的电子化临床技术能力和商业化服务结合在一起的一体化解决方案，可帮助我们的客户更加顺畅、经济和高效的推动整个研发历程。