Tianjin GoalGen Biotechnology Co., Ltd. is the sole subsidiary of Clin-nov Medical,a subsidiary of Asymchem(002821.SZ).    Tel:+86-022-25322880

中文 | EN
Message

Home
About Us
Business
Advantage
News
Join Us
Contact Us
Location:Home > Join Us > job
Clinical QA manager (tianjin/Beijing)
  • Job Responsibilities:

  • 1. Responsible for establishing and maintaining the quality management system of the department;

  • 2. Responsible for the quality control and management of drug clinical trials, conduct an audit of the clinical trial process according to GCP and company SOP, and propose relevant opinions to improve the quality of clinical trials;

  • 3. Responsible for establishing employee GCP and SOP training system.

  • job requirements:

  • 1. Clinical Pharmacology, Clinical Medicine, Pharmacy or above;

  • 2.5 years and above QA experience;

  • 3. Have working experience in large pharmaceutical companies and CRO companies;

  • 4. Have excellent ability to express, organize and coordinate.


  • Registered manager (tianjin)
  • Job responsibilities:

  • 1. Participated in the management of the registration team and served as the project leader;

  • 2. Analyze and evaluate registered projects and formulate registration strategies;

  • 3. Responsible for maintaining customer relations and expanding potential customers;

  • 4. Establish and maintain good working relationships with customers and the drug regulatory department;

  • 5. Formulate the management system of the department.

  • Job requirements:

  • 1. Pharmacology, pharmacy, chemical analysis or related majors, master degree or above, more than 5 years of experience in drug registration;

  • 2. Proficient in Microsoft word, PowerPoint, Excel, etc.;

  • 3. Deeply understand and master the policies, regulations and technical requirements related to registration;

  • 4. Good interpersonal skills (oral and written) and negotiation skills;

  • 5. Good ability to find and solve problems independently, effective time management ability;

  • 6. Cet-6 or above, proficient in listening, speaking, reading and writing;

  • 7. Experience in registration of innovative drugs and biological products is preferred.


  • Clinical project manager (tianjin/Beijing)
  • Job responsibilities:

  • 1. Fully responsible for the quality control and management of clinical research projects, responsible for the supervision of key centers, and ensure that the experimental projects are carried out in strict accordance with the program, SOP and relevant laws and regulations;

  • 2. Developed the general schedule of the project, assisted CRA centers to complete the schedule of each center, completed the comprehensive start, execution and completion of the test project as planned, and effectively communicated and coordinated with other personnel related to the project, such as medical writing, data and statistics, etc.;

  • 3. According to the developed test plan, complete the corresponding case report form, original medical record, project management form and other documents, and submit them to the superior for review;

  • 4. Reviewed clinical research contracts of each center, and guided CRA to complete the negotiation and signing of research contracts with each center;

  • 5. Before the overall launch of the project, conduct pre-launch training for project team members, and promote the launch of each center as planned; Maintain effective communication with all relevant personnel and conduct routine quality control and progress reporting during the project;

  • 6. Fully responsible for the teaching and training and daily management of CRA members of the project team, assist CRA in developing the monitoring plan, and assist the project manager in developing the collaborative monitoring plan to carry out the collaborative monitoring selectively to ensure the progress and quality of the test;

  • 7. Complete other tasks assigned by superior leaders.

  • Job requirements:

  • 1. Bachelor degree or above, 3 years or above clinical trial project management experience;

  • 2. Having expert resources in the industry and maintaining good relations is preferred;

  • 3. Familiar with ich-gcp, GCP and relevant management regulations;

  • 4. Basic understanding of the operation process, trial process and regulations of different departments of clinical trials;

  • 5. Good daily and emergency management skills;

  • 6. Independent working ability and strong team spirit, able to integrate into and contribute to the team;

  • Able to travel frequently.


  • Medical manager (tianjin)
  • Job responsibilities:

  • 1. Presided over the work of the medical department, including medical writing and support, data management and statistics, etc.;

  • 2. Designed clinical research programs for new drugs, planned clinical trials in each phase, developed relevant documents for clinical trials, took into account management analysis and statistical data, and guided medical specialists to write clinical trial reports;

  • 3. Responsible for the management of the department, clarify the post responsibilities, carry out regular department training, and formulate the department performance appraisal system;

  • 4. Visited clinical experts independently and established good relations with them;

  • 5. Investigated domestic and foreign new drug research information, and made research reports.

  • Job requirements:

  • 1. Doctor or master degree in clinical medicine or clinical pharmacology, medical background is preferred;

  • 2. Familiar with GCP and other relevant laws and regulations, understand the drug research and development process, and participate in the guidance of preclinical research related trials;

  • 3. Stable working attitude, good sense of teamwork, strong organizational, coordination and communication skills; Enterprising spirit and good learning ability, honest quality;

  • 4. Able to work under high pressure;

  • 5. Experience in cancer drug development or clinical work is preferred.


  • Marketing manager (tianjin/Beijing)
  • Job responsibilities:

  • 1. Collecting business information and making business development plans;

  • 2. Responsible for business development, including external publicity, target customer search, etc.;

  • 3. Develop potential clients among drug r&d enterprises, colleges and universities, and hospital researchers;

  • 4. Assisted in completing the project plan and contract;

  • 5. Negotiate with customers and promote cooperation;

  • 6. Tracked the completion of the contract and communicated with customers timely;

  • 7. Maintain customers and ensure long-term cooperation.

  • Job requirements:

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

  • 2. Have certain knowledge of China's drug and medical device registration and management regulations and clinical trials;

  • 3. Experience in pharmaceutical business or drug r&d, experience in CRO industry is preferred;

  • 4. Good at communication, strong communication and negotiation ability, affinity and customer service awareness;

  • 5. Proactive, innovative, team player, able to work under pressure;

  • 6. Strong learning ability, strong sense of responsibility and ability to solve problems independently;

  • 7. Good image and good temperament.


  • Management Trainee (Tianjin)
  • Job description:

  • The “Management Trainee” program is one of the construction programs for the Guanqin Medical Talent Echelon and aims to train future leaders. The company has developed detailed personal development plans for outstanding fresh graduates with comprehensive quality and potential, systematic training, creating a multi-post mobile learning platform, rapidly improving their professional quality, and gradually transferring them to various management positions.

  • You will be able to rotate in these departments:

  • The marketing department, with its excellent ability to withstand stress and communication, is a very challenging job.

  • The clinical department has medical and pharmacy expertise, likes to engage in clinical research work, and has a good sense of service and teamwork.

  • The Department of Medicine has medical and clinical medical expertise, English writing ability and accessibility to medical professional literature, and has good self-management and motivation.

  • The registration department has expertise in pharmacy, pharmacology, and chemical analysis. It is familiar with the laws and regulations on drug registration and the registration process. It has an enterprising spirit and good learning ability.

  • The clinical QA department has medical related professional knowledge, good writing ability, can independently write documents, and has high logical thinking ability and execution ability.

  • 1 Management training students orientation training; starting from the company's grassroots posts;

  • 2 In 1-3 years, it developed into the backbone of the company's grassroots management;

  • 3 training direction: office management staff, market management, clinical project management, etc.

  • job requirements:

  • 1.2019 graduates, majors in medicine, pharmacy, bachelor degree or above;

  • 2. Actively participate in community activities and off-campus practice activities, and be preferred as a student union or other community cadre;

  • 3. Have strong professionalism, leadership and learning ability, good analytical and problem solving skills;

  • 4. Hard work, stress resistance, communication skills, do not mind high-intensity business trips.

  • Clinical Project QA Specialist (Tianjin)
  • Job Responsibilities:

  • 1. Assist QA in the improvement, maintenance and improvement of the company's quality management system;

  • 2. Conduct audits of clinical trial projects in accordance with company system documents, SOPs, and project QA plans;

  • 3. Ensure that clinical trials are performed in accordance with the protocol, GCP (or ICH-GCP) and company system and SOP requirements;

  • 4. Keep an eye on industry-related regulations and regularly organize company employees to conduct GCP and SOP training;

  • 5. Combine the inspection situation of the project, propose the addition and modification of the unsuitable item, and improve and improve the SOP of the clinical project QA;

  • 6. Supervise and track the implementation of non-compliance improvement measures in the clinical department;

  • 7. Complete other work arranged by the department head.

  • job requirements:

  • 1. Bachelor degree or above, major in medicine;

  • 2. Have more than two years of system work experience in relevant industries;

  • 3. Familiar with CFDA, FDA related regulations and guidelines;

  • 4. The work is rigorous and meticulous, with high logical thinking ability, communication ability and execution ability;

  • 5. Can independently write documents, manage documents, and skillfully use office office software;

  • 6. Can adapt to business trips.

  • Medical Promotion (Tianjin)
  • Job Responsibilities:

  • 1. Plan, organize and implement important public relations events (such as forums, seminars, client events, etc.) and evaluate the results of the activities;

  • 2. Responsible for the operation and maintenance of the company website, WeChat public account, the writing and dissemination of related soft texts, and independently coordinate and handle the relationship with all aspects;

  • 3. Responsible for the expansion and maintenance of the company's external media relations, writing relevant press releases of the company to various media, and organizing relevant media promotion activities;

  • 4. Complete other related work matters that the leadership confesses.

  • job requirements: 

  • 1. Bachelor degree or above in medicine, public relations, journalism, etc.;

  • 2. Familiar with the operation mode of the public or media industry, with relevant media resources and relationship channels are preferred;

  • 3. Familiar with various forms of planning writing, can independently plan and organize related activities;

  • 4. Cheerful and generous, positive attitude, good interpersonal communication skills, open-minded and good at expressing;

  • 5. Agile thinking, unique creativity, excellent writing, strong logic, meticulous work style and strong execution.

  • Marketing Specialist (Tianjin/Guangzhou)
  • job requirements: 

  • 1. Have the ability to independently develop large customers in the industry and have certain sales experience;

  • 2. Bachelor degree or above in medicine, pharmacy or related major;

  • 3. Have certain knowledge of Chinese pharmaceutical and medical device registration management regulations and clinical trials;

  • 4. Have experience in pharmaceutical business or drug research and development, and have been engaged in business workers in the CRO industry;

  • 5. Clear conditioning, quick thinking, strong negotiation ability, certain affinity, customer service awareness;

  • 6. Results-oriented, self-motivated, innovative and team-oriented, able to withstand certain work pressures;

  • 7. Strong learning ability, strong sense of responsibility and ability to solve problems independently;

  • 8. Good image and good temperament.

  • Job Responsibilities:

  • 1. Collect business information and develop business development plans;

  • 2. Participate in relevant exhibitions and publicize;

  • 3. Multi-channel customer development, collecting and integrating potential customer information, contacting and opening new customers;

  • 4. Negotiate with customers to promote cooperation;

  • 5. Assist in completing the project plan and project contract;

  • 6. Track the completion of the contract and communicate with the customer in a timely manner;

  • 7. Maintain customers and ensure long-term cooperation;

  • 8. Complete other related work matters that the leadership confesses.

  • Registration Commissioner (Tianjin)
  • Job Responsibilities: 

  • 1. Responsible for the overall supervision, tracking and management of the company's pharmaceutical, medical device and health food registration projects, timely communication with customers, coordination of relevant issues at various stages of project operation, and completion of project work reports on time;

  • 2. Responsible for the registration, writing and completion of registration of registered drugs, medical devices and health foods, tracking registration progress and obtaining registration information in a timely manner; (1) Organizing departments according to drug, medical device, health food registration regulations and guidelines The personnel shall write the application materials according to the drug registration category; 2 track the progress of the review and the progress of the sample inspection, and communicate with the relevant departments in time to ensure the registration progress and the registration materials for drugs, medical devices and health foods meet the requirements;

  • 3. Responsible for communication with the Drug Administration, Drug Inspection Center and other departments;

  • 4. Responsible for the writing and reporting of fund application materials;

  • 5. Complete other tasks for leadership delivery.

  • job requirements: 

  • 1. Pharmacy or related major, master's degree or above, relevant work experience is preferred;

  • 2. Proficiency in the application of Micorsoft word, PowerPoint, Excel, etc.;

  • 3. Familiar with the laws and regulations on drug registration and the registration process, familiar with the organization of drug declaration materials, and understand the technical requirements for drug development and related guiding principles;

  • 4. Have a steady and steady working attitude, good sense of teamwork, strong organizational, coordination and communication skills; enterprising spirit and good learning ability, honest quality;

  • 5. Prior to being a class or community cadre during school.

  • Medical Statistics (Tianjin)
  • Job Responsibilities:

  • 1. Provide support for the preparation of clinical trial protocols, including statistical design, sample size calculation, randomization and blinding;

  • 2. Responsible for writing statistical reports for clinical trials;

  • 3. Clinical data management work;

  • 4. Provide guidance and training for clinical research personnel, and provide statistical consultation and guidance for other teams.

  • job requirements:

  • 1. Medical statistics, health statistics, biostatistics and other related majors, master's degree or above, undergraduate students with rich experience may also consider;

  • 2. Familiar with statistical methods of clinical trials, proficient in common data statistics software;

  • 3. Work carefully, have good communication skills and teamwork spirit;

  • 4. Experience in clinical trial statistics is preferred.

  • Medical support (Tianjin)
  • Job Responsibilities: 

  • 1. Medical frontier information tracking, medical/pharmacy literature inquiry, information collection;

  • 2. Provide comprehensive medical support and technical support to the personnel of the marketing department;

  • 3. Complete project development planning according to customer needs and write PPT;

  • 4. Assist the marketing department to communicate professionally with customers;

  • 5. Can complete other related work assigned by the superior leadership.

  • job requirements:

  • 1. Background of medical pharmacy, bachelor degree or above;

  • 2. Relevant work experience is preferred;

  • 3. Fluent in English, able to read medical professional literature without barriers, and have good English writing ability;

  • 4. Skilled application of office office software (PowerPoint, Word, Excel, etc.);

  • 5. Have clinical trial experience, program or SCI article writing, PPT production experience is preferred;

  • 6. Organized logically, work proactively, practically and conscientiously, with good self-management and motivation.

  • Clinical Auditor CRA (Tianjin/Guangzhou)
  • Job Responsibilities:

  • 1. Through the standardized monitoring process, complete the clinical trial and inspection work on time, and ensure that the test is carried out in strict accordance with the requirements of the test plan, SOP and GCP;

  • 2. Responsible for the coordination, inspection and quality control, progress supervision, reporting, document management, etc. of the clinical trial center;

  • 3. Communicate with the researcher and negotiate to solve the problems, and coordinate the relationship between the research project leader, clinician, auxiliary department, clinical base, and patients;

  • 4. Conduct clinical trial-related training for the research center in charge;

  • 5. Coping with audits and audits; preparing and providing the required documents for the sponsors; and cooperating with other functional departments;

  • 6. Complete other tasks assigned by the line manager and/or project manager (PM).

  • job requirements: 

  • 1. Bachelor degree or above in medicine or pharmacy;

  • 2. Knowing the clinical trial management practices (GCP) and clinical work related regulations are preferred; clinical or CRA work experience is preferred;

  • 3. Prior to being a class or community cadre during school;

  • 4. Strong communication and coordination skills and good language skills, team spirit and strong sense of responsibility;

  • 5. Optimistic and cheerful, able to withstand pressure, able to think and solve problems independently;

  • 6. Can adapt to frequent business trips.

  • Medical Writing (Tianjin)
  • Job Responsibilities:

  • 1. Search, read, translate and collate relevant literature, and cooperate with the medical manager to complete the collection, design and production of medical materials and clinical information;

  • 2. Write, edit the trial protocol and clinical summary report in accordance with the medical document writing guidelines and CFDA requirements;

  • 3. Can cooperate with the medical manager to complete the medical research work of the new project;

  • 4. Be able to independently retrieve and edit medical information, and cooperate with the medical manager to complete the medical information related to the clinical project;

  • 5. Assist in providing medical support during clinical trials;

  • 6. Be able to complete other medical editorial work assigned by the medical manager.

  • job requirements:

  • 1. Medical background, best clinical medicine, master's degree or above;

  • 2. Two years and above relevant work experience;

  • 3. Fluent in English, able to read medical professional literature without barriers, and have good English writing ability;

  • 4. Skilled application of office office software (PowerPoint, Word, Excel, etc.);

  • 5. Have clinical trial experience, program or SCI article writing, PPT production experience is preferred;

  • 6. Organized logically, work proactively, practically and conscientiously, with good self-management and motivation.

  • Doctor of Medicine (Tianjin)
  • Job Responsibilities:

  • 1. Hosting the work of the Ministry of Medicine, including medical writing and support, data management and statistics;

  • 2. Design a clinical research program for new drugs, plan clinical trials for each phase, and formulate relevant documents for clinical trials, taking into account management analysis statistics; direct medical professionals to write clinical trial reports;

  • 3. Responsible for departmental management, clarify job responsibilities, conduct regular departmental training, and develop departmental performance appraisal system;

  • 4. Visit clinical experts independently and establish good relationships with them;

  • 5. Investigate information on new drug research at home and abroad, and develop research reports.

  • job requirements:

  • 1. Doctoral or master's degree in clinical medicine or clinical pharmacology, with medical background preferred;

  • 2. Familiar with relevant laws and regulations such as GCP, understand the drug development process, and participate in guiding pre-clinical research related experiments;

  • 3. Have a steady and steady working attitude, good sense of teamwork, strong organizational, coordination and communication skills; enterprising spirit and good learning ability, honest quality;

  • 4. Can withstand strong work pressures;

  • 5. Experience in oncology drug development or clinical work is preferred.

  • Copyright © 2018-2019 Copyright Tianjin Guanqin Pharmaceutical Technology Co., Ltd.        Powered by:kbyun.com