Job Responsibilities

1. conduct center screening and center qualification assessment before conducting clinical trials;

2. To be responsible for the supervision of clinical trials and the production of trial related documents according to the requirements;

3. Conduct comprehensive supervision and management of the research centers in accordance with protocols, SOPs and GCP;

4. complete the start-up, execution and closure of clinical trials in the center on time;

5. report the progress of the trial on a monthly basis or as required by the program, and communicate with PM to report any problems encountered.

Posting Requirements

1. specializing in clinical pharmacy, medicine and nursing;

2. Mastery of clinical trial quality management standards and familiarity with the clinical trial process;

3. Clear written and oral expression skills, good communication;

4. Excellent teamwork ability;

5. Able to adapt to frequent business trips, able to withstand high work pressure.

Job Responsibilities

1. responsible for assisting the company's related business marketing, project negotiation and customer contact work, on behalf of the company for customers to explain and promote the company's services;

2. actively seek and maintain target customers to facilitate project cooperation;

3. Communicate the important information of the company and the industry to customers in a timely manner, cultivate and maintain good relations with customers;

4. assist in the development of new customers, customer maintenance, to explore customer service needs;

5. responsible for the feasibility study of potential projects of customers;

6. responsible for assisting in the writing of contracts, tenders, quotations, service plans, contact (reply) letters, etc., responsible for project quotations, tenders and contracts and other related documents to determine, to ensure that the signed project in accordance with the contract agreement;

7. be responsible for the contract management of the project, including contract review, negotiation, signing, delivery, execution and termination;

8. be responsible for following up the progress of the project and later tracking the collection of money, invoicing and so on;

9. tracking customer service requirements of the company to provide the most timely information;

10. assist in the new signing, actual collection to promote the existence of problems in a timely manner to communicate and propose solutions;

11. assist other departments of the company to communicate with customers, so that the smooth operation of the company's business.

Posting Requirements

1. Bachelor degree or above, preferably in medicine, pharmacy, bioengineering related majors;

2. excellent fresh graduates, with more than 1 year related experience in SMO industry or CRO enterprises is a plus;

3. Skilled in using office software, honest and cheerful, proactive, with good professional ethics;

4. good teamwork spirit, good coordination, communication and ability to deal with critical incidents;

5. strong written and verbal skills, able to assist in completing project requirements sorting and PPT document writing;

6. strong ability to work independently.

Job Responsibilities

1. Administers medication to subjects, records, enters data into the system, and draws blood to send samples if needed.

Posting Requirements

1. College degree or above;

2. Nursing related majors, with a nurse's license, with some work experience is preferred;

3. Good communication and coordination skills, good appearance, clean and tidy, stable and easy-going;

4. Experience in clinical research is preferred.

Job Responsibilities

1. responsible for drafting and reviewing data management plan;

2. Participate in eCRF design;

3. Responsible for drafting and reviewing the data verification plan;

4. Responsible for database creation and testing;

5. Responsible for data verification and challenge management;

6. Responsible for external data reception and processing;

7. Responsible for laboratory data reception and processing;

8. Verification of SAE consistency;

9. Responsible for medical coding as well as medical coding QC;

10. Participate in final data quality control and data (blind) review sessions;

11. Responsible for database locking and unlocking;

12. Responsible for drafting and reviewing data management reports;

13. Responsible for the establishment and management of DM project documents;

14. Other work arranged by supervisor.

Posting Requirements

1. Bachelor degree or above, majoring in pharmacy, medicine, computer, mathematics and other related majors;

2. no experience required, have knowledge of clinical trials, can master more than 3 data management work after receiving training;

3. be able to accept occasional overtime work according to the project progress;

4. Have the spirit of research and strong logical thinking ability;

5. Proficient in Word, Excel, PowerPoint;

6. English grade 4 or 6, proficient in reading and writing.

Job Responsibilities

1. responsible for statistics related work in clinical trial program;

2. understand clinical trial protocols, SAP and other related documents;

3. writing SAS programs, or calling SAS programs to create analytical data sets;

4. writing SAS programs, or calling SAS programs to build statistical data lists, statistical tables;

5. be responsible for the design of experiments, complete sample size estimation and calculation of statistical test efficacy;

6. writes statistical analysis plans, including the design of analytical forms for studies;

7. Responsible for randomization and blinding;

8. work with the data manager to construct the database and identify key variables in the database;

9. Write SAS programs to generate tables, lists, graphs and statistical analyses;

10. Participate in blind audits and work with the Data Manager to develop blind audit reports;

11. write statistical analysis reports and perform proofreading and quality control of analytical data sets (ADSs), tables, charts, and tables of data (TFLs) produced by programmers;

12. Cooperate with the project leader to complete the checking of analysis results;

13. Other duties as arranged by supervisor.

Posting Requirements

1. Bachelor degree or above, majoring in statistics, biostatistics, health statistics, pharmacy, medicine, mathematics and applied mathematics, preventive medicine, public health and other related fields;

2. at least one year experience in SAS programming;

3. be able to work with SAS for statistical analysis;

4. have the spirit of research and strong logical thinking ability;

5. Proficient in the use of SAS, Word, Excel, PowerPoint;

6. English grade 4 or 6, read and write skillfully.

Job Requirements

1. responsible for the preparation of clinical research related materials (CRF, investigator's manual, review, summary report, etc.);

2. medical literature search, translation of medical literature, writing related documents and reports;

3. Medical review of clinical data, including AE, laboratory data, vital signs, medical history, combined medication and other data cleaning medical support;

4. medical audit: responsible for reviewing protocol deviations, subject enrollment eligibility, AE codes, statistical analysis reports, etc.

Posting Requirements

1. Bachelor degree or above in clinical medicine, pharmacy related majors;

2. strong ability to search and read English literature;

3. Familiar with GCP and other clinical related regulations;

4. 1 year or more experience in clinical supervision or medical writing in pharmaceutical companies or CRO industry is preferred;

5. strong logical analysis, writing organization skills, good communication and learning ability.

Job Responsibilities

1. Responsible for on-site supervision and verification of the company's clinical trial program to ensure that the trial is conducted in accordance with relevant standard operating procedures, experimental protocols, and GCP regulations, identifying problems and making recommendations, and submitting audit reports in a timely manner;

2. Responsible for regular inspection of clinical trial documents, inspectors' work summaries and plans and other relevant information, and timely submission of audit reports;

3. Communicate with project managers, inspectors and investigators in a timely manner to ensure that the clinical trials comply with GCP and SOP specifications;

4. Follow up the problems found during the audit work and solve them in a timely manner;

5. Reasonably designate the audit plan and organize its implementation;

6. Complete other tasks assigned by the leadership.

Posting Requirements

1. Bachelor degree or above in medicine, pharmacy related majors;

2. familiar with drug registration management, GCP regulations and relevant regulations on clinical research;

3. have rich experience in monitoring, familiar with project management and monitoring process, familiar with the trial program;

4. Strong written expression, oral expression and communication and coordination skills;

5. team spirit, strong sense of responsibility, strong ability to develop and implement plans, and suitable for business trips.

Job Responsibilities

1. responsible for the overall management and time control of clinical programs;

2. responsible for communication and coordination with clinical research centers and sponsors;

3. be responsible for the communication and coordination with the internal functions of the company related to the clinical project;

4. responsible for CRA work arrangement, management, and project related training;

5. responsible for the preparation of clinical project related documents.

Posting Requirements

1. Master's degree in clinical medicine, pharmacy and other related fields;

2. more than 2 years of project management experience;

3. good knowledge of clinical trial related laws and regulations and clinical trial process; 

4. good English listening, speaking, reading and writing skills.

Job Responsibilities

1. responsible for the daily operation and management of DMPK department;

2. provide guidance to solve DMPK key and difficult problems, review study protocols and reports, and supervise project completion;

3. be responsible for providing preclinical and translational medicine DMPK results, supporting the optimization of lead compounds, selection of drug candidates, IND studies;

4. collaborate on study protocol design for clinical DMPK;

5. efficiently executes project management and interacts closely with other functional groups or departments to ensure that projects are carried out according to predefined protocols and plans.

Position Requirements

1. Master's degree or above in pharmacokinetics, bioanalysis, pharmacology or other related majors, more than 6 years of relevant work experience for Master's degree, more than 3 years of relevant work experience for PhD (work during postgraduate period is counted as work experience);

2. Experienced in liquid-liquid coupling analysis, familiar with the relevant requirements, guidelines and regulations of CDE, and experience in the declaration of new drug IND is preferred;

3. Good learning ability, good research quality and problem solving ability;

4. Strong communication and coordination skills and teamwork spirit.

Job Responsibilities

1. writing bioanalytical research protocols;

2. using liquid chromatography - tandem mass spectrometer to complete the development of analytical methods for samples, method validation, and biological samples testing work, maintenance of instrumentation and equipment, to solve simple instrument failure;

3. Write, process and analyze the relevant experimental records and write analysis reports;

4. Completion of project archiving, data preservation and project verification.

Position Requirements

1. Bachelor degree or above in medicine related majors, more than 2 years of pharmacokinetic related work experience;

2. able to skillfully use HPLC, LC-MS/MS and other related instruments, and perform basic maintenance of the instruments;

3. able to complete the development and validation of bioanalytical methods and testing of related samples;

4. conscientious, strong learning ability and good interpersonal communication skills;

5. patient and responsible, able to trace back and solve problems arising in the course of experiments.