Johnson & Johnson 职业机会

Beijing-R&D-Senior Clinical Research Specialist

Beijing, 中国
Clinical Research non-MD


职位描述

Requisition ID: 1700194294W

Responsible for the design, planning, implementation, and overall direction of clinical research projects. Designs experimental protocols and writes trial protocols outlining the purpose and methodology of a trial, and patient record forms. Conducts clinical studies of products that have been determined to satisfy a medical need and/or offer commercial potential. Works with management to establish the essential conditions necessary to determine the safety, efficiency, medical usefulness, and marketability of drug and product candidates. Evaluates and analyzes complex clinical data. Applies an advanced knowledge of principles, theories, concepts in the field plus a working knowledge of other related disciplines. Interprets complex results of investigations in preparation for governmental new drug applications. Verifies that source data and documents and other trial records are accurate, complete and maintained. Oversees activities to ensure compliance with protocol and overall clinical objectives. Ensures adverse events, concomitant medications, and inter current illnesses are reported in. Provides imaginative, thorough and practicable solutions to a wide variety of difficult problems. Interfaces with marketing or research project teams and government regulatory agencies to provide technical consultation.
资历
Responsible for the design, planning, implementation, and overall direction of clinical research projects. Designs experimental protocols and writes trial protocols outlining the purpose and methodology of a trial, and patient record forms. Conducts clinical studies of products that have been determined to satisfy a medical need and/or offer commercial potential. Works with management to establish the essential conditions necessary to determine the safety, efficiency, medical usefulness, and marketability of drug and product candidates. Evaluates and analyzes complex clinical data. Applies an advanced knowledge of principles, theories, concepts in the field plus a working knowledge of other related disciplines. Interprets complex results of investigations in preparation for governmental new drug applications. Verifies that source data and documents and other trial records are accurate, complete and maintained. Oversees activities to ensure compliance with protocol and overall clinical objectives. Ensures adverse events, concomitant medications, and inter current illnesses are reported in. Provides imaginative, thorough and practicable solutions to a wide variety of difficult problems. Interfaces with marketing or research project teams and government regulatory agencies to provide technical consultation.
主要地点
中国-北京-Beijing
组织
- 强生(上海)医疗器材有限公司
工作
Clinical Research non-MD
Requisition ID
1700194294W