1. Have years of experience as a medical affairs manager in a CRO or pharmaceutical company; have experience in large-scale clinical projects or hospital clinical work; have participated in clinical research on anti-tumor registration and cellular immunotherapy; able to write clinical research protocols and determine adverse events;

2. Have good teamwork ability and strong scientific research thinking; maintain good cooperative relationship with CRO companies and researchers, and safeguard the interests of the company in the cooperation;

3. Familiar with the diagnosis and treatment process of common clinical diseases, and have a deep understanding and insight on the epidemiology and clinical research of diseases.

1. Responsible for phase I-III clinical trials, medical support and monitoring; determining the research and development direction of species; literature research, analysis and writing of relevant clinical reports;

2.Responsible for registration and declaration; responding to clinical medical questions during pre-clinical/clinical project review, and participating in the defense of the expert review meeting if necessary.

Oriental Garden Building, Building 104, IT Industrial Park, Electronic City, #10 Courtyard A, Jiuxianqiao North Road, Chaoyang District, Beijing

1. Have at least 3-5 years of experience in oncology clinical project management, with phase 1-3 or full-cycle clinical trial management experience;

2. Have good organization, communication and time management skills, and able to establish effective interpersonal communication;

3. Have working experience in well-known CRO/SMO or foreign pharmaceutical company; can accept business trips.

1.Formulate clinical research project management plans, risk management plans and budgets, and organize the management and implementation before, during and after clinical research projects; be responsible for the management and organization of pre-, intermediate and post-clinical documents and costs;

2. Be responsible for assisting the drafting, formulation, distribution, revision and archiving of clinical trial research documents;

Oriental Garden Building, Building 104, IT Industrial Park, Electronic City, #10 Courtyard A, Jiuxianqiao North Road, Chaoyang District, Beijing

1. Able to carry out work independently, have strong communication and coordination ability and persuasive ability; two years of experience in oncology project is preferred;

2. Familiar with CTMS and EDC system.

1. Mainly responsible for monitoring before, during and after the clinical trials, and coordinating and solving problems and emergencies during the clinical trials;

2. Responsible for project start-up, filing, grouping, visit, distribution and management of drug information, data tracing, and archiving of process documents; assisting in organizing various meetings and support.

SCRA office address: Oriental Garden Building, Building 104, IT Industrial Park, Electronic City, #10 Courtyard A, Jiuxianqiao North Road, Chaoyang District, Beijing

CRA office address: Floor 4, Building 6, Blue Biomedical Industrial Park, Qingdao High-tech Zone