Senior Scientist in Pharmacological Research

RegeneCore Biotech·
南京
2w ago
RecruitmentUnknownPhD
Market Rate — Computer User Support Specialists
25th
$45K
Median
$58K
75th
$74K

BLS 2024 data (national)

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.

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.
RegeneCore Biotech

RegeneCore Biotech

BIOTECHNOLOGY

Nanobody Screening Technology

LocationChina - Nanjing
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