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Address: 20 Maguire Road, Suite 103, Lexington, MA 02421(America)
Tel: +1(626)986-9880
Address: Allia Future Business Centre Kings Hedges Road Cambridge CB4 2HY, UK
Tel: 0044 7790 816 954
Email: marketing@medicilon.com
Address: No.585 Chuanda Road, Pudong New Area, Shanghai (Headquarters)
Postcode: 201299
Tel: +86 (21) 5859-1500 (main line)
Fax: +86 (21) 5859-6369
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Business Inquiry
Global:
Email:marketing@medicilon.com
+1(626)986-9880(U.S.)
0044 7790 816 954 (Europe)
China:
Email: marketing@medicilon.com.cn
Tel: +86 (21) 5859-1500
Responsibilities:
1. Responsible for the entire process management of research and development stages, including the formulation of toxicological research plans for preclinical research projects, control of research quality and progress, and resolution of key technical difficulties.
2. Conduct accurate safety assessments and analytical research on ongoing varieties to study potential clinical toxicity.
3. Responsible for the review and revision of GLP toxicological test plans and formal reports, guiding the preparation of pharmacological and toxicological application materials.
4. Communicate with clients to advance project progress.
5. Establish a scientific project supervision and management system to complete research and development work on time, with quality, and in quantity.
Requirements:
1. Master's degree or above, in fields such as pharmacy, medicine, toxicology, veterinary medicine, or related disciplines.
2. Familiarity with the processes and models of new drug development, possession of GLP toxicology knowledge and experience in toxicological testing, capable of organizing and coordinating preclinical toxicological research activities.
3. Understanding of domestic and international GLP regulatory requirements and related guidelines for preclinical safety evaluation.
4. Knowledge of the new drug development process, the interconnection between toxicology, pharmacodynamics, and pharmacokinetics research, skilled at connecting related research stages, and preferably capable of promoting the smooth progress of systematic drug development evaluation.
5. Possesses strong team management abilities.
Responsibilities:
1. Maintain effective communication with management, project leaders, associate researchers, topic leaders, laboratory managers, etc., review the upcoming project proposals in a timely manner, and provide feedback to the relevant personnel. This includes executing experimental projects in accordance with SOP, GLP, experimental protocols, and under the guidance of topic leaders, while maintaining effective communication with relevant personnel and reporting.
2. Independently complete pathological examination of local tissue sections and issue pathological reports.
3. Conduct pathological examination of long-term toxicity projects under the guidance of a pathologist and issue pathological reports.
4. Perform other duties as assigned by the company.
Requirements:
1. Master's degree or above in pathology, oncology, veterinary pathology, or related fields.
2. Proficient in written and spoken communication skills.
3. Skilled in using Microsoft Word, Excel, and Access software.
4. Keen observation skills; ability to think independently; a minimum requirement for continuous problem-solving abilities.
5. Preference will be given to those with experience in reviewing slides from long-term toxicity and carcinogenicity tests, as well as experience in handling data and writing reports.
Responsibilities:
1. According to the topic arrangement of the team leader or supervisor, rationally plan the experimental scheme and schedule;
2. Standardize experimental operations, obtain reasonable experimental results, ensure progress and rational output, and truthfully report, and handle analytical data such as compound spectra in a standardized manner;
3. Consult literature, communicate and report to the supervisor, and promptly solve problems and difficulties encountered during the experiment;
4. Write experimental notebooks and compound synthesis reports in a standardized manner, ensuring authenticity and timeliness;
5. Strictly abide by company rules and regulations and EHS requirements, and participate in company organized training as required to ensure standardized and safe work.
Requirements:
1. Bachelor's/Master's degree in organic chemistry, applied chemistry, or other related chemical fields;
2. Possess a certain foundation in organic chemistry, and be familiar with basic experimental procedures for organic synthesis, product isolation, and purification;
3. Master literature retrieval methods and have the ability to read and write English literature as well as keep experimental records;
4. Strong sense of responsibility, with good teamwork spirit and communication skills.