Position responsibility:
1. Medical monitoring plan formulation;
2. Review the result of the inspection result report form;
3. Review the protocol deviation and criteria of inclusion and exclusion;
4. SAEs assessment;
5. Write final report of medical monitoring;
6. Provide medical training in therapeutic area, protocol, and other medical-related contents.

Qualifications & Requirements:
1. Medical related majors such as clinical medicine, preventive medicine, medical imageology, medical laboratory science, ；
2. Master degree or above;
3. Proficiency in English reading and writing.

Position responsibility:
1. Medical monitoring plan formulation;
2. Review the result of the inspection result report form;
3. Review the protocol deviation and criteria of inclusion and exclusion;
4. SAEs assessment;
5. Write final report of medical monitoring;
6. Provide medical training in therapeutic area, protocol, and other medical-related contents.

Qualifications & Requirements:
1. Medical related majors such as clinical medicine, preventive medicine, medical imageology, medical laboratory science, pathology, etc. preferred;
2. Master degree or above;
3. Proficiency in English reading and writing.

Position responsibility:
1. Find domestic and foreign literature and information, timely track, collect, and organize the research trends and data analysis of relevant diseases and products at home and abroad.
2. Medical review of various materials’ translation from Chinese to English or English to Chinese; 
3. Under the leadership of the superior, participate in the formulation and review of clinical study protocol and the writing of final report, ensure the timeliness of the feedback of clinical trial data and the standardization of the trial process;
4. Other works assigned by the superior.

Qualifications & Requirements:
1. The full-time graduate enrolled through national unified entrance exam, master's degree or above, major in medicine or pharmacy;
2, More than one year of relevant work experience preferred, excellent fresh graduates are also eligible, proficiency in English, can understand English reports;
3. Good communication skill, organization and coordination skill, can work under pressure;
4. Proficiency in MS Office, familiar with relevant laws and regulations of national drug study

Position responsibility:
1. Complete statistical work related to clinical trials under the leadership of the company's senior statistician, including but not limited to: study program design and writing, sample size calculation, generating random coding, blinding, generating statistical analysis plans, participating in CRF design, participating in building clinical trial database, hosting or participating in (blind) data review meetings, preparing statistical analysis procedures, performing statistical analysis of data, and writing statistical reports;
2. Provide consultation in statistics to and communicate project work with customers and colleagues in other departments;
3. Participate in the translation and collation of documents related to the company's internal statistics;
4. Consult statistics related literature and submit reports;
5. Review the documentation from DM, SAS Programmer and PM, and present Comments;
6. Serve as a part-time PM when needed, responsible for external communication for the Biostatistics Department;
7. Assist in the development and implementation of departmental standard operating practices related to biostatistics;
8. Complete other work arranged by the department leader.

Qualifications & Requirements:
1. Master's degree or above in epidemiology, biostatistics, or public health;
2. Have good statistical knowledge and SAS application experience;
3. Have a certain basic knowledge of clinical trials;
4. Good logical ability and written and verbal communication skills, skilled presentation skills and strong persuasiveness, good communication with people with different backgrounds and abilities;
5. Proactive work attitude, good cooperation with colleagues, and can work under pressure;
6. Proficiency in Windows and MS Office including Outlook, Word, Excel and PowerPoint;
7. Good English listening, speaking, reading and writing skills.

Position responsibility:
1. Develop programs to conduct statistical analysis in accordance with the statistical analysis plan or other requirements document;
2. Organize and lead projects team to advance projects, provide technical guidance to and communication with customers;
3. Review the submitted materials of projects team;
4. Implement training in CDISC related knowledge;
5. Assist in formulation of SAS programming related SOP, template and operation manual;
6. Assist in the development of SAS tools, build the company's SAS program framework, and write and store common macros;
7. Follow up the latest SAS programming technology application at home and abroad, assist in solving difficult problems in the work of SAS team;
8. Other work assigned by the leadership.

Qualifications & Requirements:

1. Bachelor degree or above in preventive medicine, mathematics, statistics, or computer related majors, more than 5 years of industry experience;
2. Have more than three years of relevant work experience, experience in large CRO or pharmaceutical companies is preferred;
3. Proficiency in SAS/Base, SAS GTL, familiar with SAS/STAT, SAS Macro;
4. Proficiency in CDISC related knowledge and guiding principles, rich experience in related projects;
5. Rich project operation experience, project leader experience is preferred;
6. Strong English listening, speaking, reading and writing skills and verbal and written communication skills, good documentation habits;
7. Strong resistance to stress and be enterprising;
8. Strong sense of responsibility, strong communication skills and team awareness.

Position responsibility:
1. Prepare relevant documents for clinical laboratory data management (such as data management plan DMP, CCG, DVP, DRP, etc.), and be responsible for saving, updating and filing;
2. Responsible for the design of the Medical Record Form (CRF) and the validation and user acceptance test (UAT) of the EDC system;
3. Complete the entry, verification, inspection and maintenance of data in CRF table and external electronic data;
4. Perform manual verification in accordance with the data verification plan, conduct medical verification if necessary, and resolve data challenges.
5. Responsible for data review and consistency check for serious adverse event before database lock-in;
6. Conduct data export and generate listing report for clinical statistical analysis;
7. Responsible for quality control of the entire process, as required by relevant laws, regulations and guidelines;
8. Responsible for medical coding and review;
9. Responsible for communication within the team (DBD/PM/MA/SS) and with the sponsor (PM/MA/DM) to solve project and data problems;
10. Prepare data management training and EDC training for PI/CRA within the department.

Qualifications & Requirements:
1. Bachelor degree or above in medical information, medical English, pharmacy, clinical or related majors;
2. More than 5 years of experience in clinical trial data management, including at least 3 years of project management experience;
3. Good communication skills in both Chinese and English;
4. Good organizational skills and project management skills;
5. Have rigorous work attitude, a high sense of responsibility, initiative, and have team spirit.

Position responsibility:
1. Responsible for the data management of clinical projects to ensure the accuracy, integrity and safety of clinical data;
2. Participate in the writing and revision of clinical trial protocols.                           
3. Write data management related documents, such as data management plan (DMP), timeline for the whole data management process and so on.
4. Responsible for the design of the Case Report Form (CRF), annotating CRF (aCRF), completing the data entry guide, completing the data entry interface verification and user acceptance test (UAT).
4. Write a Data Verification Plan (DVP), complete the Edit Check UAT, and complete other work before the data acquisition system goes live.
5. For Paper Study, issue DCF regularly, and follow up the process of DCF until all the queries in the DCF are resolved; For the EDC study, ensure the system can issue the query normally, check the process of query until the query is completely resolved.
6. Issue project progress reports within the prescribed times; conduct regular SAE consistency checks, issue queries, and follow up clinical and security databases until problems are resolved;
7. Supervise the coding staff to complete the coding of the adverse events accompanying medication and other issues.
8. Complete database locking related work, including data cleaning, audit, prepare file for database locking, and so on.

Qualifications & Requirements:
1. Bachelor degree or above in medicine, pharmacy, biology, computer science, etc.;
2. Good English level, with CET 6 or above;
3. Good communication and coordination skills;
4. Good organizational and planning skills, strong learning ability;
5. Experience in clinical data management, CRA, CRC, and SAS, SPSS and other statistical analysis tools. Experience in programming and database is preferred.

Position responsibility:
1. Responsible for the quality control and management of clinical study projects, and for the monitoring of key site if necessary, ensure that the trial projects are carried out in strict accordance with the program, SOP and relevant regulations;
2. Communicate with the sponsor or supervisor, conduct site selecting, identify the principal investigators and participating investigators, complete the overall cost budget of projects in a timely manner and submit it to the superior for approval;
3. Develop a general schedule of projects, assist the CRA of each site to complete the schedule of each site, complete the initiation, execution and closing of the trial project as planned, and communicate and coordinate effectively with other personnel (e.g., in position of medical writing or data and statistics) related to projects as needed;
4. According to the established trial protocol, complete the corresponding case report form, original medical record book and project management form and other documents and materials, submit it to the superior for review; submit the site's materials to leader unit for ethical review, and obtain the ethics approval letter for the site;
5. Responsible for the budget and procurement of trial materials, including the printing, distribution and transportation of case report forms and informed consent forms;
6. Review the clinical study contracts of each site to guide the CRA and the sites to complete the negotiation and signing of the study contract;
7. Before projects's full initiation, train projects team members, and promote each site’s initiation as planned; review all the reports of projects team members, maintain effective communication with all relevant personnel, and conduct routine quality control and progress reporting during project execution; 
8. Fully responsible for the training and daily management of projects team members (CRA), assisting the CRA to develop an monitoring plan. At the same time, as a project manager, develop a collaborative monitoring plan to selectively conduct collaborative monitoring to ensure the progress and quality of the trial;
9. Responsible for communication and coordination with Data Management Department, Biostatistics Department and Medical Affairs Department, and complete data management plan/report, statistical analysis plan/report, Q & A, data review meeting, summary meeting and final report, etc. as planned;
10. Assist other tasks assigned by the superior.

Qualifications & Requirements:
1. Bachelor degree or above in clinical medicine or clinical pharmacy;
2. More than 3 years of experience as a CRA with adequate knowledge, ability and quality; at least 2 years of work experience in PM position;
3. Proficiency in computer and office software;
4. Works independently as well as in a team environment; can be a member of and contribute to the team;
5. Excellent written and verbal communication, good at active communication with enthusiasm, interaction with different types of clients/investigators to keep good relationships, service consciousness and customer-centric awareness;
6. Have excellent team organization skills and project management skills, such as organizing project team meetings, quickly responding to problems and coming up with solutions;
7. Excellent training and presentation skills.

Position responsibility:
1. Prepare and deliver trial materials, daily express delivery and printing trial materials.
2. Project monitoring and monitoring report writing.
3. Assist in organizing clinical study related meetings. 
4. Responsible for trial drug management and blood sample delivery.
5. CRF collection and delivery. 

Qualifications & Requirements:
1. Bachelor degree or above in medicine, pharmacy or nursing (Please do not apply for the position if your major is not listed above!).
2. Proficiency in computer and office software; 
3. Outgoing personality, good communication skills, and the courage to accept challenges and work pressure.
4. Experience in clinical supervision is preferred.

Position responsibility:
1. Report to the responsible Deputy Director, responsible for CRA team management, including but not limited to CRA team formation, training, team building, etc.;
2. Responsible for the preparation or update of CRA annual training, team building, communication and other planning documents and follow-up the execution, responsible for the update of work guidance materials such as CRA work guidance;
3. Responsible for docking with projects manager, equip projects with CRA and conduct CRA workload management, and conduct CRA performance appraisal with reference to CRA performance in projects;
4. Timely feedback of problems in the CRA team management process;
5. Keep good internal and external communication.

Qualifications & Requirements:
1. Bachelor degree or above in medicine related major;
2. ACRM requires more than 3 years of clinical study operations experience, CRM requires more than 5 years of clinical study operations experience;
3. Have personnel training experience, at least 1 year CRA team management experience;
4. Work proactively, willing to accept challenges, have good psychological quality and stress resistance, have good internal and external communication and coordination skills, and have a strong sense of responsibility;
5. Excellent English ability is preferred.

Position responsibility:
1. Responsible for the development and expansion of the company's domestic and international business;
2. Responsible for finding new customers and exploring new business cooperation models;
3. Maintain customer and manage projects, complete annual performance indicators;
4. Communicate important information of the company to customers in a timely manner, and cultivate and maintain good relations with customers;
5. Participate in regional bidding work;
6. Confirm project quotation and relevant contract documents, ensure project to be executed in accordance with the contract;

Qualifications & Requirements:
1. Bachelor degree or above, major in medicine, pharmacy or marketing
2. At least 2 years of relevant business or clinical study project management experience in pharmaceutical companies or CRO.
3. Have a good ability in preparation of business promotional materials and business presentation;
4. Good English ability for daily communication, consulting relevant literature and writing project progress reports;
6. Willingness to travel.