上海招聘

·       Designing protocols and programs.

·       Overseeing all technical and scientific activities and in-life monitoring.

·       Communicating with sponsors.

·       Writing reports and evaluating data.

·       Serving as the scientific representative on corporate committees.

·       Attending scientific meetings.

·       Training of junior technical and scientific personnel.

·       Carry out R&D in line with company objectives.

QUALIFICATIONS

Education / Requirements / Skills

·       Bachelor’s degree in a related field, and a minimum of 4 years of relevant experience in biocompatibility testing, surgical modeling, implantation of medical devices, including in vitro and in vivo; OR Master’s degree in related field and 2 years of relevant experience in research testing, including in vitro and in vivo.

·       Serves as the Study Director for GLP studies and is the single point of control for straightforward multidisciplinary in vivo Medical Device preclinical projects.

·       Uncomplicated (routine) to complicated complex preclinical study design and protocol development.

·       Develops testing strategy; troubleshoots test article preparation issues.

·       Upon completion, assembles and reviews data, and determines the results and conclusions of the study.

·       Evaluates, analyzes and interprets data and presents in a clear, well-organized, scientifically sound report.

·       As necessary, prepares protocol submissions for IACUC review and responds to committee comments/questions.

·       Excellent written and verbal communication skills and interpersonal relationship skills.

·       Demonstrated problem-solving and critical thinking skills.

·       Moderate knowledge and understanding of biology principles, theories and concepts.                                                                   

·       Advanced proficiency in Microsoft Office Suite, including Word, Excel, and PowerPoint.

·       Advanced problem-solving skills and strict attention to detail.

·       Knowledge of Good Laboratory Practices (GLP) supporting a medical device environment.

·       Ability to interact professionally with all organizational levels.

·       Ability to manage competing priorities in a fast-paced environment.

·       Project management preferred

苏州药明康德成立于2006年10月，是药明康德全资子公司，该设施面积达三万多平方米并且目前向全球客户提供符合GLP标准的遗传毒性实验服务，并通过了AAALAC的国际认证； SFDA的GLP认证；欧洲OECD的GLP认证；是全球***一家通过全面资质认证的药物安全性评价中心。
同时，苏州药明康德拥有众多获得资格认证的毒理学家和病理学家们，能够为国内外客户提供包括大小动物的急性毒性、长期毒性、药代/毒代、生殖毒性、安全性药理、遗传毒性等药物安全性评价项目以及体内外药物筛选、药理药效研究等临床前安全评价研究服务。