Director, Clinical Research
Work Place: Shanghai
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-
Release Time:2023-09-29
Responsibilities:
1. Designing and implementing clinical trials in oncology under GCP, ICH-GCP and other relevant clinical research guidelines;
2. Providing medical monitoring and guidance during clinical trials;
3. Communicating with regulatory authorities on medical affairs and preparing medical research documents for registration;
4. Providing medical support throughout clinical development;
5. Providing medical advice on business development strategies (e.g. product portfolio, co-development, in-/out-licensing, etc.);
6. Maintaining effective communication and cooperation with investigators, ethics committees, clinical research institutions, patient groups, and regulatory authorities at all levels in accordance with relevant regulations and policies.
Qualifications:
1. A master’s or doctorate degree in medicine;2. Familiar with GCP/ICH guidelines and FDA/NMPA regulations;
3. Comprehensive and in-depth understanding of the whole process of clinical trials for new drugs;
4. At least 3 years of clinical trials experience in oncology.
ORA Director/Associate Director
Work Place: Shanghai
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Shanghai
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Pudong New Area
Release Time:2023-09-30
Description of job
Small molecule drug direction
Mainly responsible for the company registration department, including Sino-US new drug Pre-IND/IND application, new drug Pre-NDA/NDA application. Cooperate with small molecule drug CMC and toxicology projects to ensure timely completion and provide high-quality deliverables.
Qualifications
1. Education: Bachelor degree or above in pharmacy or related majors.
2. Skills: good English reading and writing skills (apply to FDA, all email materials are in English, and spoken language is not required);
3. Experience: Understand the relevant regulations and technical guidelines such as new drug registration and application, and understand the drug research and development process, production and inspection expertise;
4. Have more than 3 years of relevant work experience in drug registration, and be responsible for the registration and declaration of a small molecule project. Experience in small molecule new drug registration application and data writing is preferred.
5. Quality: Serious and rigorous work attitude, strong learning ability, strong execution ability, strong sense of responsibility, good teamwork and communication skills.
CV delivery:HR@bivisionpharma.com
Peptide Synthesis Researcher
Work Place: Shanghai
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Shanghai
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Pudong New Area
Release Time:2023-09-30
Job requirements:
1.Bachelor degree or above in organic chemistry, medicinal chemistry, applied chemistry or related majors;
2. Bachelor degree above 2 years, master degree at least 1 year experience in peptide synthesis, more than 2 years experience in peptide synthesis is preferred
3. Familiar with various acid-amine condensation conditions, good at finding problems in project progress, and able to
enough to solve problems independently;
4. Able to record the experimental steps in detail and analyze the experimental results, be good at analyzing spectra and writing synthesis reports;
4. Proficient in the separation and purification techniques and structure identification methods of compounds commonly used in laboratories, such as NMR, HPLC, LC-MS, combi-flash, high-pressure preparative liquid phase, etc.;
5. Able to proficiently use various chemical literature search tools for literature search, and proficient in reading English literature;
6. Have good communication skills and team spirit
CV delivery:HR@bivisionpharma.com
Chemical Synthesis Researcher
Work Place: Shanghai
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Shanghai
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Pudong New Area
Release Time:2023-09-30
Job Responsibilities:
1. Be able to carry out multi-step organic synthesis reactions, skillfully complete the setting and tracking of chemical reactions, purify and characterize the products, and make reasonable and comprehensive analysis of the analysis results obtained;
2. Able to conduct literature search and independently solve problems in experiments;
3. Able to actively participate in various technical discussions;
4. Make clear and complete experimental records, write experimental reports and summaries;
5. Good laboratory operation skills, abide by the rules and regulations of the laboratory, and do a good job in laboratory safety protection;
6. Complete other tasks assigned by department leaders
Job Requirements:
1. Organic chemistry, medicinal chemistry, applied chemistry and other related majors, bachelor degree or above;
2. Bachelor degree for more than 2 years, master degree for more than 1 year related experience in organic synthesis, experience in new drug research and development is preferred;
3. Have a solid theoretical foundation of organic chemistry, be familiar with various organic reactions, and have proficient laboratory skills;
4. Able to complete the synthesis work from small batch (mg level) to large batch (kg level);
5. Have a strong sense of responsibility, a serious and responsible work attitude, be able to bear hardships and stand hard work, be good at communicating with people, and have a good team spirit;
CV delivery:HR@bivisionpharma.com
Analytical Researcher
Work Place: Shanghai
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Shanghai
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Pudong New Area
Release Time:2023-09-30
Job Responsibilities:
1. Proficient in the basic principles of organic compound analysis, able to use analytical instruments to complete the development and detection of analytical methods for samples, and to analyze the results;
2. Responsible for the management of the analytical laboratory, formulate various rules and regulations of the laboratory, and complete various tasks;
3. Actively do a good job in the daily maintenance of analytical instruments, assist in solving instrument failures, and calibrate instruments and equipment on time;
4. Provide analysis support for the synthesis and other departments, and be responsible for the security of various analysis data;
5. Make clear and complete experimental records, write experimental reports and summaries;
6. Implement the company's intellectual property protection, safety, hygiene and other norms to ensure the smooth implementation and implementation of various systems;
7. Complete other tasks assigned by department leaders.
Job Requirements:
1. Bachelor degree or above in organic chemistry, pharmaceutical analysis, analytical chemistry, applied chemistry and other related majors;
2. More than 2 years of undergraduate degree, and more than 1 year of relevant experience in analytical chemistry and biologically active substances research for master's degree;
3. Familiar with the establishment of analytical methods of HPLC, LCMS and other instruments and equipment, and be able to proficiently operate related instruments and equipment;
4. Those with the following relevant experience are preferred: more than 1 year of relevant work experience in drug quality research and application, able to develop analytical methods, verify analytical methods, establish quality standards, and be able to independently write drug quality research and stability research. Application materials; familiar with the drug registration regulations and technical guidelines of FDA, ICH, CFDA and CDE, and familiar with the drug registration application process and technical requirements;
5. Conscientiously make experimental records and write project reports;
6. Active in work, serious and responsible, able to bear hardships and stand hard work, good at communicating with people, and have a good team spirit;
CV delivery:HR@bivisionpharma.com
Senior Researcher
Work Place: Shanghai
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Shanghai
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Pudong New Area
Release Time:2023-09-30
Job Responsibilities:
1. Familiar with various literature retrieval methods, and be able to complete the preliminary design of compound synthesis routes through literature review;
2. Have good execution ability, be able to analyze the problems in the experiment in time, propose reasonable solutions, and modify the synthesis route;
3. Have the ability to carry out multi-step organic synthesis reactions to prepare biologically active substances, analyze the SAR of synthetic substances, propose reasonable improvement plans, and speed up the project development process;
4. Have good analytical and problem-solving skills, and be good at using the basic principles of organic chemistry to solve various problems in work;
5. Have leadership skills, manage organic synthesis laboratories, be responsible for the safety of synthesis laboratories, and be able to assist in leading and managing research assistants' new drug research and development work;
6. Complete the work assigned by other leaders.
Job Requirements:
1. Ph.D. degree, major in medicinal chemistry, organic chemistry, 0-2 years of work experience in related fields, more than two years of experience is preferred;
2. Familiar with the process and methods of new drug research and development, understand the mechanism of organic chemical reactions, have strong problem-solving ability, and innovative thinking;
3. Have good organic synthesis skills and be able to carry out multi-step synthesis reactions to prepare compounds with biological activities;
4. Able to use various modern analysis and characterization methods (HPLC, LCMS, NMR) to analyze and characterize the synthesized compounds;
5. Good communication and writing skills, able to
6. Serious and responsible work, practical and willing to work, diligent and dedicated, strong sense of responsibility, good leadership and teamwork spirit;
7. Experience in peptide synthesis is preferred.
CV delivery:HR@bivisionpharma.com
Senior Scientist
Work Place: Jiangsu Province
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Nanjing City
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Pukou District
Release Time:2023-09-30
Description of job
1. Responsible for participating/leading the establishment, design, implementation and promotion of the company's R&D projects.
2. Establishment and optimization of the drug in vitro activity test method of the project; screening of active drugs.
3. Exploration of target pathway mechanism.
4. Exploration and establishment of in vivo pharmacodynamic model.
5. Complete other tasks assigned by the leader.
Qualifications
1. Bachelor degree or above, major in cell biology, biochemistry, pharmacy or related fields;
2. More than two years of work experience;
3. Have good scientific research literacy, rigorous research ideas, and standardized experimental operations;
4. Have team awareness and initiative.
CV delivery:HR@bivisionpharma.com
Scientist (Changshu)
Work Place: Jiangsu Province
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Suzhou City
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Changshu City
Release Time:2023-09-30
Description of job
1. Investigate new product information, track the latest research progress at home and abroad, and formulate product development plans;
2. Radiochemical labeling, analysis and other related work;
3. Responsible for the design, implementation and summary of the research plan, and responsible for the writing of application materials;
4. Organize the project team to carry out research work according to the research plan, and solve various problems arising from the research process;
5. Assist in laboratory management and other laboratory-related daily work;
6. SOP establishment and implementation
7. Participate in the construction of drug development project team.
8. Complete other tasks assigned by the leader.
Job requirements
1. Master's degree, with the following related majors: radiopharmaceuticals, organic chemistry, analytical chemistry, biochemistry, pharmacy, biology, radiophysics and other related majors;
2. Familiar with new drug research and development, understanding of drug analysis methods; understanding of radiopharmaceuticals, tumor drug research and development is a priority.
3. Strong research ability, able to independently research relevant information of new drugs;
4. Proficiency in Chinese and English literature retrieval;
5. Have good communication skills, teamwork spirit, easy-going, innovative and exploratory spirit.
CV delivery:HR@bivisionpharma.com
Scientist (Shanghai)
Work Place: Shanghai
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Shanghai
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Huangpu District
Release Time:2023-09-30
Description of job
1. Responsible for participating in the implementation and promotion of the company's R&D projects.
2. Establishment and optimization of the drug in vitro activity test method of the project; screening of active drugs.
3. Analyze the biological activity of small molecule drugs and screen high-quality small molecule drugs.
4. To study the mechanism of action of the drug by in vitro experiments.
5. Assist in laboratory management and other laboratory-related daily work
6. SOP establishment and implementation.
7. Complete other tasks assigned by the leader.
Job requirements
1. Have good teamwork ability, be honest and credible, be patient and careful, have strong hands-on ability, and love laboratory work.
2. Biology, pharmacy, oncology, immunology and related majors; bachelor degree or above, experience in cell culture, activity test and WB test is preferred; fresh graduate students, with cell culture, activity test and WB test during the study period Experience is preferred.
3. Work experience is not limited, those with CRO company or new drug research and development work experience are preferred;
CV deliveryHR@bivisionpharma.com
CONTACT US
Tel:
Mail:
Address:
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