Recruiting talents, welcome to join!

Resume delivery mailbox:ykrcx@ykrcx.comTel:+86-10-82001093

Number of recruits
Work place
Release time
Recruitment
Number of recruits
-
Work place
Beijing/Tianjin
Release time
2019-10-23
Recruitment
Project Leader (Preparation Direction)
Job Responsibilities:
1. Responsible for the daily management of preparation research room.
2. Organize the formulation of research plans for various projects, organize and implement the implementation of various projects, solve key technical problems, and obtain research results;
3. Review of relevant technical materials such as phased summary reports and application materials
4. Instruct the staff in this room to carry out and complete subject research, and conduct professional training regularly;
5. Organize and implement product pilot scale-up.
6. Assist other departments to complete relevant technical indicators, patents and articles in the process of project application, implementation, and conclusion;
7. Accept and support the management of superior departments, implement and complete the assigned tasks.

Job Requirements:
1. Bachelor degree or above, major in Chinese pharmacy, pharmaceutical preparations or related;
2. More than 5 years of R&D experience in chemical raw materials or Chinese medicines;
3. Familiar with regulatory documents such as drug management regulations, drug registration regulations, etc.; familiar with drug research related regulations such as application material requirements and technical guidelines.
Number of recruits
1
Work place
Beijing
Release time
2019-10-23
Recruitment
Project Manager (Clinical Direction)
Job Responsibilities:
1. Responsible for the overall management and supervision of clinical research projects and complete the overall start, execution and termination of clinical trials on time;
2. Cooperate with the marketing department in project analysis, evaluate the feasibility of the project and propose solutions, assist in the completion of the project evaluation and drafting of the plan;
3. Screen research centers according to the company's SOP;
4. Organize clinical trial program seminars and clinical trial summary meetings;
5. Organize researcher representatives and statisticians to blindly compile drugs;
6. Training CRA, including trial protocol, ICF, CRF, research medical records, researcher memo card, etc.;
7. Review the supervision plan, reasonably divide the work of the CRA; review the progress submitted by the CRA and the progress of the project, and coordinate the overall progress of the project; coordinate the PI and the statistical analyst to hold a blind review meeting;
8. Coordinate the communication among research centers, sponsors, and data management personnel.

Job Requirements:
1. Bachelor degree or above, major in medicine;
2. Good communication skills, integrate into the team, good at learning, willing to collaborate and share;
3. Have strong stress resistance and psychological endurance, and have strong resilience and willpower in the face of challenging tasks;
4. Ability to use office software such as office proficiently;
Number of recruits
-
Work place
Luzhou
Release time
2019-10-23
Recruitment
CRA
Job Responsibilities:
1. Carry out overall management of the research center in charge, strictly follow GCP, SOP, test plan and related laws and regulations, and complete the selection, start-up, routine inspection, and center closure of the research center on time within the project schedule;
2. Responsible for research, selection, research center and researcher related information. Provide test-related information in time according to the test progress.
3. Organize, prepare and participate in researcher meetings, and be responsible for the liaison and reception of center researchers;
4. Obtain clinical trial documents and ethics committee approval within the project plan time limit, and conduct a preliminary review of the ethics committee approval.
5. Independently complete the clinical supervision of related projects and formulate a reasonable supervision plan;
6. Assist the research center to report AE/SAE and follow up.
7. Through the verification of the original data, ensure the authenticity, accuracy and completeness of the data, while ensuring the safety and interests of the subjects;
8. The management office is responsible for the test items of the research center, including test drugs, test documents and test related equipment.

Qualifications:
1. Bachelor degree or above;
2. More than half a year of relevant work experience, master degree can be extended to fresh graduates;
3. Medicine, nursing, clinical medicine, integrated Chinese and Western medicine and other related medical majors.
Number of recruits
-
Work place
Beijing/Shanghai/Guiyang
Release time
2019-10-23
Recruitment
CRC
Job Responsibilities:
1. In accordance with relevant national regulations, research plans, hospital and company SOP requirements, and under the authorization of the researcher, assist the researcher to complete various tasks:
2. Assist in completing SAE related safety reports;
3. Assist the researcher to fill in the case report form, and assist the researcher to complete the collection, sorting and filing of documents of the research center at each stage of the experiment;
4. Assist researchers to complete the work of subject screening, enrollment, follow-up, etc., including subject recruitment, screening of potential subjects, arranging subject visits, arranging laboratory examinations, obtaining inspection results, etc.;
5. Assist CRA's central inspection work, prepare various documents in advance for CRA's inspection, and report the progress of the research center to CRA in a timely and comprehensive manner;
6. Assist CRA and researchers to complete data Q&A in time;

Qualifications:
1. Bachelor degree or above;
2. More than half a year of relevant work experience, master degree can be extended to fresh graduates;
3. Medicine, nursing, clinical medicine, integrated Chinese and Western medicine and other related medical majors.

Scan the WeChat QR code


彩票平台