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Nanjing RegeneCore Biotech Co.,Ltd. is an innovative start-up company under the Regene Group, advocating for scientific culture, emphasizing the co growth of employees and enterprises, and maintaining human health.

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Clinical Operations Director 面议 Time:2024-04-24 点击查看更多
工作地点: 南京 - - 所属部门: Recruitment 工作年限: No limit 学历: No limit 招聘人数: 1
Job Description: 1. Fully responsible for planning, implementing, operating, and managing clinical trial work; 2. Manage the clinical supervision team, responsible for team building and development; 3. Responsible for the entire process of clinical trials in research and development projects, including plan formulation, selection of clinical trial sites, effective project implementation, and quality control; 4. Participate in the development of clinical trial plans, including overall project progress plans, timelines, budgets, and manpower arrangements; 5. Track and inspect the completion status of each stage of the project, track the execution of experiments, promptly identify and solve problems, and ensure the quality and progress of experiments; 6. Responsible for communicating and exchanging key review experts, clinical experts, and other clinical research resources related to clinical research, assisting in developing correct clinical research strategies and plans, thereby ensuring the smooth progress of clinical research; 7. Responsible for summarizing and reviewing clinical trials, organizing clinical research meetings, and approving clinical trials; Responsible for managing and communicating to resolve issues related to conducting clinical research; 8. Responsible for the construction and training management system of clinical teams, establishing and regularly improving institutional processes related to clinical operations; 9. Provide necessary technical support related to clinical trials according to the company's development needs. Job requirements: 1. Doctoral degree in clinical medicine, pharmacy, or related fields; 2. At least three years of experience in clinical research project management (in foreign companies, large and medium-sized domestic pharmaceutical companies, or CRO companies); 3. Good coordination, communication, and pressure resistance skills, with foresight and innovative thinking; 4. Has a strong sense of responsibility, a positive work attitude, meticulous work, and patience; 5. Familiar with the entire process of drug research and development, as well as the development and current status of clinical research both domestically and internationally; 6. Good English communication and writing skills.
Medical Director 面议 Time:2024-04-24 点击查看更多
工作地点: 南京 - - 所属部门: Recruitment 工作年限: No limit 学历: No limit 招聘人数: 1
Job Description: 1. Responsible for formulating clinical development strategies for new drugs; 2. Fully responsible for the formulation of clinical trial plans for new drugs and the writing, review, and revision of medical related documents; 3. Responsible for the overall management and technical control of medical review, medical supervision, medical analysis, and medical support during clinical trials; 4. Communicate and coordinate with external medical experts and review experts to ensure project execution. 5. Conduct medical research, analysis, and information support for the determination of new projects; 6. Responsible for the department management and operation of the Medical Department, including the development and review of work plans, work standards and processes, personnel organization and management, and the development of departmental performance evaluation plans and supervision of execution. Job requirements: 1. Integrity, high sense of responsibility and team spirit, strong communication and coordination skills; 2. Doctoral degree in clinical medicine, pharmacology, oncology, and related fields; At least three years of clinical medical experience in pharmaceutical companies or CRO for new drugs; 3. Familiar with clinical trial management processes, familiar with GCP, ICH-GCP, drug registration regulations, and various pharmaceutical policies. 4. Strong ability to search Chinese and English literature and medical information, as well as write reports.
Senior Scientist in Pharmacological Research 面议 Time:2024-04-24 点击查看更多
工作地点: 南京 - - 所属部门: Recruitment 工作年限: No limit 学历: No limit 招聘人数: 1
Job Description: 1. Responsible for preclinical research on pharmacology, toxicology, PK, pharmacodynamics, and other aspects of the IND application for the company's macromolecular drug research and development project; 2. Responsible for developing preclinical pharmacological and toxicological research plans and plans for ongoing projects, as well as establishing friendly cooperative relationships with CRO companies in collaboration with the company, tracking experimental progress, reviewing relevant plans and reports, and jointly promoting the progress of the company's projects; 3. Responsible for supervising the execution, tracking, management, and progress of pharmacological and toxicological experiments conducted by the cooperating CRO company, helping to solve problems in the experiments, and ensuring the timely completion of the project with high quality and quantity; 4. Responsible for supervising the quality of collaborating CRO companies and reviewing research data to ensure the accuracy and reliability of experimental results; Analyze test data and interpret test results, and review and sign test reports; 5. Responsible for writing new drug application materials related to pharmacology, toxicology, PK, pharmacodynamics and other experiments, and collaborating with relevant departments such as the registration department to complete the new drug application work; 6. Responsible for collecting, analyzing, and evaluating literature on the pharmacology and toxicology of new drugs for research and development projects. Job requirements: 1. Doctoral degree in pharmacy, toxicology, or medical related fields 2. Having complete non clinical project work experience is preferred; 3. Having rich professional knowledge and experience in preclinical toxicology, pharmacokinetics, and efficacy in the field of anti-tumor, as well as experience in writing pharmacological toxicology INDs; 4. Familiar with the regulatory requirements of domestic and international GLP and relevant guidelines for preclinical safety evaluation, with experience in applying for new drug IND, and strong ability to search and read Chinese and English literature; 5. Have good communication and coordination skills, a positive work attitude, and a good team spirit.
Senior Scientist in Antibody Engineering 面议 Time:2024-04-24 点击查看更多
工作地点: 南京 - - 所属部门: Recruitment 工作年限: No limit 学历: No limit 招聘人数: 1
Job Description: 1. Lead the team to carry out new antibody construction and proprietary drug development related to the development of biological macromolecular drugs; 2. Construction of phage display library; 3. Construction of bifunctional antibodies; 4. Mature antibody affinity; 5. Humanization of antibodies; 6. Optimize and improve the antibody structure to meet the requirements of drug formation. Job requirements: 1. Doctoral degree in molecular biology, biochemistry, genetic engineering, bioengineering, and related fields; 2. Having at least five years of experience in biological laboratories related to antibody engineering; 3. Track industry trends and understand cutting-edge technologies for developing new antibodies; 4. Proficient in vector construction, primer design, PCR operation, gene retrieval, plasmid extraction, phage library construction, and other experimental techniques; 5. Experience in practical development of bifunctional antibodies, phage display, antibody affinity maturation, and antibody humanization are preferred; 6. Priority given to engaging in antibody engineering research in biopharmaceutical enterprises.
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TEL:

025-58608860

Address: Room 07 Building 16 Treehouse, No. 73, Tanmi Road, Jiangbei New District, Nanjing

Enterprise email:rjk@regenecore.com

 

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