CONTACT US

Contact Us

Contact Us


We operate strictly according to the actual needs of our customers and provide them with comprehensive services, earning their trust and support.

Eurasia Huizhi (Beijing) Medical Research Co., Ltd

Address: Room 3008, Floor 3, Building I, Yingkun Century, No. 6 Courtyard, East Road of the Automobile Museum, Fengtai District, Beijing

Fax: 010-83739030

Postal code: 100070

Email: bd-oyhz@healtech.com.cn (Business Cooperation)

ouyahuizhi-hr@healtech.com.cn (Resume Submission)

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Job Posting


Job Openings

Number of positions available

Educational requirements

Age limit

Salary and benefits

View details

Registration Manager

2

Undergraduate

5-10 years

To be negotiated

Registration Manager Job Description: 1. Complete the relevant research and evaluation work for the initiation of innovative drug projects. 2. Develop the budget, plan, progress tracking, and summary for innovative drug registration projects. 3. Be responsible for the organization and implementation of registration applications, including regulatory research, strategy development, preparation of registration documents, and submission of registration applications. 4. Review registration application materials and ensure timely completion of submissions within the prescribed deadlines; track the status of subsequent document submissions and the review and approval process. 5. Coordinate and prepare for on-site inspections during the application process. 6. Maintain relationships with leaders, experts from drug regulatory authorities, and applicants; establish and maintain a network of domestic and international authorities and expert resources related to drug registration, thereby enhancing the company’s positive image. 7. Timely obtain information on national policies, regulations, reforms, and the latest guidelines concerning pharmaceuticals, registration, and R&D; promptly and effectively communicate new regulations and adjust departmental workflows accordingly; collect and organize domestic and international pharmaceutical regulations and medical information to provide evidence and recommendations for company decision-making and the advancement of registration projects. 8. Perform other tasks assigned by the leadership. Job requirements: 1. Bachelor’s degree or above in pharmacy, biology, clinical medicine, or a related field, obtained through regular enrollment; English proficiency at or above CET-6 level. 2. More than five years of experience in pharmaceutical registration, with a thorough understanding of the relevant policies and regulations governing innovative drug registration applications, familiarity with the complete procedures for innovative drug registration, experience in collaborating with domestic and international drug regulatory agencies, and the ability to independently undertake and lead pharmaceutical registration tasks. 3. Strong capabilities in retrieving, analyzing, and researching information on innovative drug registration, excellent project management skills, and proven experience and creative approaches to problem-solving. 4. A strong sense of responsibility, excellent communication skills, the ability to work independently, teamwork skills, and a capacity for continuous learning. Benefits: Five social insurances and one housing fund, equity incentives, project awards, paid annual leave, weekends off on Saturdays and Sundays, regular medical checkups, and holiday benefits. Submission email: ouyahuizhi-hr@healtech.com.cn

Registration Officer

5

Undergraduate

1-3 years

To be negotiated

Registration Officer Job Responsibilities 1. Assist the supervising leader in conducting regulatory analyses for drug registration and carrying out project research, among other tasks. 2. Follow up on all stages of new drug registration, translate or proofread relevant documents, and, in accordance with the national classification and management requirements for new drug registration, complete the preparation, compilation, and review of drug registration application materials on time. Submit the registration documents to the pharmaceutical regulatory authorities and obtain acceptance approval. 3. Be responsible for communicating with relevant government departments, tracking and understanding project progress, and resolving any conflicts or issues that arise between research and application processes. 4. Continuously monitor and retrieve information on registration-related regulations, literature, and domestic and international registration requirements; ensure the completeness and accuracy of the project documentation under your responsibility, and archive it promptly. 5. Regularly attend internal project team meetings and client communication meetings. 6. Build and maintain positive relationships with clients, review agencies, drug inspection institutions, and other relevant parties. 7. Communicate effectively with departments such as medical affairs, clinical operations, and business development. 8. Take charge of other tasks assigned by the supervisor. Job requirements: 1. Bachelor’s degree or above in a relevant field such as biology, medicine, or pharmacy, obtained through regular enrollment. 2. At least one year of work experience in drug registration-related tasks at a pharmaceutical company or CRO. 3. Familiar with the "Drug Administration Law" as well as relevant laws, regulations, and guiding principles for pharmaceutical product registration. 4. Familiar with the preparation of submission overview documents and the requirements for organizing complete registration dossiers. 5. English proficiency at or above CET-6 level, capable of proficiently searching literature and regulations, and possessing excellent learning and communication skills. Benefits: Five social insurances and one housing fund, equity incentives, project awards, paid annual leave, weekends off on Saturdays and Sundays, regular medical checkups, and holiday benefits. Submission email: ouyahuizhi-hr@healtech.com.cn

Medical Manager

2

Master's degree

3-5 years

To be negotiated

Medical Manager Workplace: Beijing, Shanghai Job Responsibilities: 1. Retrieve, read, translate, and organize relevant literature, and be capable of collecting, designing, and preparing medical data and clinical information. 2. Write and edit project-related documents such as trial protocols and clinical summary reports in accordance with medical document writing guidelines and NMPA requirements. 3. Be capable of conducting medical research and providing business support for new projects. 4. Be able to independently conduct literature searches and edit medical information, and complete the preparation of medical information related to clinical projects. 5. Be responsible for medical verification, assessment of medical events during clinical trial execution, and medical monitoring. 6. Be responsible for participating in investigator meetings, and for effectively communicating with clinical or biostatistics experts—either leading or assisting leaders—in the drafting, revision, and finalization of protocols and reports. 7. Provide medical support throughout the clinical trial process. 8. Be able to mentor and train medical specialists in tasks related to literature retrieval, medical writing, and medical research. 9. Be capable of performing other medical editing tasks assigned by the department manager or the company. 10. Modify documents during the clinical trial process. Job Qualifications: 1. Medical background, with a preference for clinical medicine; master’s degree or higher. 2. At least 3 years of relevant work experience. 3. Fluent in English, capable of reading medical literature without difficulty, and possessing strong reading and communication skills. 4. Proficient in using office software (such as PowerPoint, Word, Excel) and skilled in creating PPT presentations. 5. Experience in clinical trials or as a clinician is preferred; prior experience in protocol writing or SCI article publication is a plus. 6. Clear and logical thinking, proactive and diligent work attitude, and strong self-management and motivation skills. Benefits: Five social insurances and one housing fund, equity incentives, project awards, paid annual leave, weekends off on Saturdays and Sundays, regular medical checkups, and holiday benefits. Submission email: ouyahuizhi-hr@healtech.com.cn

Medical Officer

5

Master's degree

1-3 years

To be negotiated

Medical Officer Workplace: Beijing, Shanghai Job Responsibilities: 1. Retrieve, read, translate, and organize relevant literature, and collaborate with the medical manager to collect, design, and prepare medical data and clinical information. 2. Write and edit trial protocols and clinical summary reports in accordance with the guidelines for medical document preparation and the requirements of the NMPA. 3. Collaborate with the medical manager to carry out medical research for new projects. 4. Independently take charge of retrieving and editing medical information, and work closely with the medical manager to prepare medical information related to clinical projects. 5. Assist in providing medical support throughout the clinical trial process. 6. Perform other medical editing tasks assigned by the medical manager. 7. Modify documents during the trial process. Job Qualifications: 1. Medical background, with a Master’s degree or higher preferred; clinical medicine is highly desirable. 2. At least one year of relevant work experience. 3. Fluent in English, able to read medical literature without difficulty, and possessing strong reading comprehension skills. 4. Proficient in using office software (such as PowerPoint, Word, and Excel). 5. Prior experience in clinical trials, as well as experience in writing protocols or SCI articles and creating PPT presentations, is a plus. 6. Strong sense of organization and logic, proactive, diligent, and meticulous in work, with excellent self-management and self-motivation skills. Benefits: Five social insurances and one housing fund, project bonuses, paid annual leave, weekend off on Saturdays and Sundays, regular medical checkups, and holiday benefits. Submission email: ouyahuizhi-hr@healtech.com.cn

Project Manager

2

Undergraduate

3-5 years

To be negotiated

Project Manager Workplace: Beijing, Shanghai, Chengdu Job Responsibilities: 1. Responsible for the comprehensive management, quality control, and supervision of the projects under your charge, ensuring timely and high-quality project delivery. 2. Responsible for providing business guidance and overseeing the execution of CRA activities within this project team, including: reviewing work plans and summary reports, assigning tasks to CRAs, promptly addressing issues arising from various centers and researchers, monitoring inspection quality, reviewing inspection reports, conducting real-time monitoring of key and challenging issues in the project, proactively identifying project risks and developing corresponding mitigation measures, supervising and ensuring adherence to project schedules, and managing materials and documentation. 3. Responsible for team-building efforts within this project team. 4. Assist the department manager in refining departmental policies and upgrading Standard Operating Procedures (SOPs), support the smooth implementation of new policies, and take the lead in effectively complying with the company’s relevant management regulations. 5. Responsible for training CRAs on project-related topics, encouraging CRAs to actively acquire professional knowledge and project management skills, and continuously enhancing their inspection capabilities. 6. Responsible for cost control of the project, strictly controlling unnecessary expenditures, and ensuring the efficiency and quality of CRA inspections. 7. Coordinate externally with various research centers, sponsors, data management personnel, and statisticians, maintaining good communication and fostering strong relationships with all parties. 8. Maintain effective communication and coordination with supervisors, other project teams, and departments; keep in touch with CRAs stationed overseas within the team, ensuring the smooth progress of the project. Job requirements: Educational Background: Bachelor’s degree or above in a medical or pharmaceutical-related field. Work Experience: More than 3 years of experience in the management of clinical trials for multiple projects; prior experience in innovative drug project management is preferred. Skills and Competencies: Familiar with the Regulations on Drug Registration, GCP guidelines, and other relevant regulations pertaining to clinical research. - Proficient in the entire process of clinical research, with a deep understanding of all stages of clinical studies and the ability to work independently. - Strong written and verbal communication skills, adept at interacting with researchers of various types. - Possesses strong organizational, coordination, communication, and problem-solving abilities. Benefits: Five social insurances and one housing fund, equity incentives, project awards, paid annual leave, weekends off on Saturdays and Sundays, regular medical checkups, and holiday benefits. Submission email: ouyahuizhi-hr@healtech.com.cn

Clinical Research Associate (CRA)

5

Undergraduate

1-3 years

To be negotiated

Clinical Research Associate (CRA) Workplace: Beijing, Shanghai, Chengdu Job Responsibilities: 1. Assist the project manager in completing center screening, organizing investigator meetings, and applying for ethical approvals. 2. Provide training to investigators, covering both regulatory requirements and specialized training for clinical trials, ensuring that investigators conduct research strictly in accordance with the study protocol and applicable regulations. 3. Develop monitoring plans and carry out multi-center clinical monitoring activities as scheduled, submitting relevant monitoring reports in a timely manner. 4. Urge investigators to promptly address and rectify any issues documented in the monitoring reports, ensuring compliance with applicable regulatory requirements. 5. Assist the project manager in conducting department kickoff meetings, coordinating and communicating with the statistics department, and preparing clinical trial summaries. Job requirements: 1. Bachelor’s degree or above in fields such as medicine, pharmacy, nursing, public health, and bioengineering; at least one year of work experience; outstanding recent graduates will also be considered. 2. Honest and responsible person. 3. Strong communication, learning, and coordination skills; optimistic and cheerful, able to handle pressure. 4. Good at and eager to continuously learn, proactively enhancing one’s abilities through further study. 5. Solid foundation in foreign languages and strong written communication skills. Benefits: Five social insurances and one housing fund, project bonuses, paid annual leave, weekend off on Saturdays and Sundays, regular medical checkups, and holiday benefits. Submission email: ouyahuizhi-hr@healtech.com.cn

Business Manager

5

Undergraduate

3-5 years

To be negotiated

Business Manager Workplace: Beijing, Shanghai, Chengdu Job Responsibilities: 1. Responsible for developing and expanding the company’s various domestic and international business operations, and representing the company in explaining and promoting its services and products to clients. 2. Collaborate with senior management to identify new customers and explore innovative business models. 3. Maintain client relationships and manage projects, while achieving specified annual business targets. 4. Serve as the company’s primary external representative, promptly conveying important information about the company and the industry to clients, and cultivating and sustaining strong, positive relationships with them. 5. Prepare project quotations and related contract documents, ensuring that signed projects are executed in accordance with the terms of the contract. Job requirements: Education: Bachelor’s degree or higher in a relevant field such as medicine, pharmacy, or bioengineering. Experience: Successful experience in independently developing key accounts; at least 3 years of work experience in business or clinical research project management at a CRO. Skill and technique: 1) Highly proficient in using various Microsoft Office software, especially Word, Excel, Access, and PowerPoint. 2) Familiar with GCP and relevant regulations. 3) Well-versed in GCP and the company’s SOPs, and skilled in handling training assessment materials and training procedures. 4) Possesses a solid network of contacts both domestically and internationally within the industry, as well as a robust business development and customer relationship network. Benefits: Five social insurances and one housing fund, equity incentives, commission-based bonuses, paid annual leave, weekends off, regular medical checkups, and holiday benefits. Submission email: ouyahuizhi-hr@healtech.com.cn

Business Specialist

5

Undergraduate

1-3 years

To be negotiated

Business Specialist Workplace: Beijing, Shanghai, Chengdu Job Responsibilities: 1. Responsible for developing and expanding the company’s various domestic and international business operations, and representing the company in explaining and promoting its services and products to clients. 2. Collaborate with senior management to identify new clients and explore innovative business models. 3. Maintain client relationships and manage projects, while achieving specific annual business targets. 4. Serve as the company’s primary external representative, promptly conveying important information about the company and the industry to clients, and cultivating and sustaining strong, positive relationships with clients. 5. Prepare project quotations and related contract documents, ensuring that signed projects are executed in accordance with the terms of the contract. Job requirements: Educational Qualification: Bachelor’s degree or above in a relevant discipline such as medicine, pharmacy, or bioengineering. Experience: Successful experience in independently developing clients; at least 1 year of work experience in business or clinical research project management at a CRO. Skill and technique: 1) Highly proficient in using various Microsoft Office software, especially Word, Excel, Access, and PowerPoint. 2) Familiar with GCP and relevant regulations. 3) Familiar with GCP and the company’s SOPs, and proficient in training assessment materials and training procedures. Benefits: Five social insurances and one housing fund, commission-based bonuses, paid annual leave, weekend off on Saturdays and Sundays, regular medical checkups, and holiday benefits. Submission email: ouyahuizhi-hr@healtech.com.cn