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 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 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 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.

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.

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.

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. 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. 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;