1. Assist in sorting out the management information of the quality control department;

2. Carry out on-site quality control and RBM quality control according to the quality control plan;

3. Supervise and urge the joint supervision of all project teams;

4. Follow up the rectification and solution of relevant problems after joint supervision , institutional quality control and external quality control of all project teams ;

5. Other affairs of quality control department.

1. Pharmaceutical, medical or related professional background, bachelor degree or above

2. Two years of excellent CRA experience can also be considered, and device project experience is preferred

3. Professional skills: strong learning ability, communication and coordination ability, analysis ability and team writing ability

4. Quality requirements: good health, good image and good temperament.

1. Assist in the formulation of sales plan and urge all sales to achieve sales targets, including the tracking of sales progress and sales contract;

2. Assist in the formulation of sales related assessment policies, and be responsible for the transmission, interpretation and implementation of the policies;

3. Sort out sales materials, manage sales contracts and other sales documents, do a good job in archiving, and assist in commercial bidding;

4. Be responsible for the statistics and analysis of sales data, and make relevant reports;

5. Update the company's website and operate official account.

1. Bachelor degree or above, major in marketing or secretarial business;

2. Strong pressure resistance, good communication skills, good English communication skills are preferred;

3. Have strong marketing and service awareness, strong adaptability, and be able to handle customer complaints independently;

4. Proficient in basic computer office software, form processing, PPT and other software.

1. Be responsible for writing, sorting and reviewing the registration and application materials of medical devices;

2. Be responsible for writing clinical evaluation of medical devices;

3. Be responsible for docking with customers, testing and evaluation institutions;

4. Be responsible for controlling the quality and progress of the registered project;

5. Be responsible for providing support for the business department and clinical department;

1. At least 3 years working experience in active medical device product registration, manufacturing or development and design;

2. Be familiar with relevant standards of active equipment and software products;

3. Be able to complete the preparation of registration materials independently;

4. Good English skills;

1. Communicate with the sponsor and investigator, and be responsible for the design and writing of clinical data such as clinical trial protocol and clinical trial report;

2. Provide medical support for the project team and provide training on medical knowledge and protocol in relevant treatment fields;

3. Assist the project in medical audit, including reviewing SAE and protocol deviation;

4. Search domestic and foreign medical literature and provide relevant medical information support;

5. Participate in the organization and implementation of clinical projects;

6. Establish good cooperation and communication relations with experts in important academic fields;

7. Carry out regular medical training for internal employees of the company;

8. Assist and cooperate with the coordination work of other departments.

1. Master degree or above, major in medicine, pharmacy, medical imaging and other related majors;

2. Proficient in Chinese and English literature retrieval, interpretation, analysis, sorting and summary writing;

3. Strong communication and coordination skills and teamwork skills.

1. Assist PM and CRA to manage trial related documents, such as collection, scanning, copying, archiving and maintenance of clinical trial research data;

2. Cooperate with PM to collect the information of research institutions from CRAs and update the project management tracker;

3. Assist in the management of test materials, and complete the distribution, recovery and destruction of project materials after the approval of the project manager;

4. Coordination of clinical trial related meetings and training, such as arrangement and recording of research meetings;

5. Other support work for CRA team.

1. Bachelor degree or above in medicine and health and other related majors;

2. Be familiar with the application of word, Excel and other office software;

3. Good Chinese expression skills, able to sort out basic English documents;

4. Have a certain understanding of clinical trials and relevant laws and regulations of domestic clinical trials;

5. Have basic communication skills, strong sense of responsibility, hard-working and willing to learn

1. Implement the supervision of the clinical research center in charge according to the supervision plan;

2. Ensure that the clinical trials of the research center are carried out in strict accordance with the protocol, GCP and relevant laws and regulations, and protect the rights and interests of subjects;

3. Assist researchers in solving possible problems during the experiment;

4. Ensure that the research data are recorded in the case report in a timely, accurate and complete manner;

5. Collect, sort out and archive the research documents according to SOP;

6. Be able to undertake the work of project assistant and assist the project manager in quality control of clinical research;

7. Complete other related work assigned by PM manager.

1. Bachelor degree or above, major in medicine or related life sciences;

2. Have strong team spirit, communication and problem-solving ability, and be able to business travel;

3. Those who have participated in formal GCP training are preferred.

1. Communication within the team and external sponsors;

2. Before the project, evaluate and estimate the staffing and estimate the time point of the project

3. Manage and ensure that all project team members receive project training

4. Manage and ensure the quality of clinical research project documents;

5. Supervise the project progress and time point to ensure that patients are enrolled and data are cleared according to the project requirements;

6. Participate in and respond to the sponsor's inspection and inspection of the project;

7. Manage the handover of personnel within the project team.

1. College degree or above in clinical, nursing and pharmacy;

2. Have more than 2 years of experience in the same position of CRC, including more than 1 year of experience in three types of medical device projects;

3. Good service awareness, strong expression and communication skills.

1. Assist the researcher to complete the management, recruitment and visit of subjects;

2. Assist researchers to complete the submission of ethical materials, and assist in the research and completion of SAE, AE and other relevant safety reports;

3. Assist in the data collection, sorting and archiving of clinical trial projects;

4. Assist in the management of device test and complete relevant records;

5. Assist researchers to cooperate with the central supervision of CRA and prepare various documents for CRA supervision in advance.

1. Nursing, pharmacy, clinical medicine and other related majors;

2. Clinical experience is preferred;

3. Strong independent working ability and teamwork spirit;

4. Have a sense of responsibility, positive and enterprising, cautious and meticulous, and strong organization.

1. Assist the project manager and clinical experts to complete the design of research scheme and other test data;

2. Be responsible for the investigation, screening, coordination, ethics review, agreement signing, supervision and quality control, recruitment progress supervision, follow-up and conclusion of clinical trial institutions;

3. Coordinate researchers, management institutions, CRC, sponsors, etc., and manage clinical trial affairs;

4. Data recovery and query resolution, assist in data management and statistical analysis;

5. Write the summary of the center and sign and seal the clinical trial documents;

6. During the training period with immature CRA skills, you need to work as a clinical research assistant (CTA)

1. Full time bachelor degree or above, major in medicine or related life sciences, fresh graduates or students without course tasks.

2. Be interested and enthusiastic in the clinical trial industry;

3. Understand relevant laws and regulations of clinical trials;

4. Those who have participated in formal GCP training are preferred;

5. Excellent academic performance and good English level;

6. Strong communication, understanding, analysis, induction, coordination, persuasion, organization and team spirit.