summary
about the company.
A biotechnology company specializing in peptide research and development, the company focuses on the production and application of peptide-based products in the fields of healthcare and pharmaceuticals.
about the team.
...
about the job.
1. Responsible for in vitro and in vivo pharmacological studies of new drug development, for drug efficacy evaluation during the new drug development process. This includes project initiation research, experimental protocol design, new method development and validation, result statistical analysis, and review of experimental reports.
2. Primarily responsible for the design of in vivo pharmacokinetic experimental protocols, participation in animal model establishment and validation, as well as drug evaluation protocol design.
3. Assist in solving difficult problems undertaken by all departments, providing solutions through literature research, consultation with internal and external experts, and supervising the successful resolution of issues.
4. Assist in the preparation of drug registration application materials.
5. Participate in communication with external clients, CRO commissioning, organization liaison, supervision coordination, and progress tracking.
6. Participate in the management of the team.
skills and experience required.
1. Doctoral degree in biology, pharmacology, or pharmacy, with more than two years of relevant work experience.
2. Able to independently design PK schemes based on drug molecular characteristics, and interpret PK data to support molecular or dosing scheme optimization. Candidates with more than two years of DMPK experience in CRO or R&D pharmaceutical companies are preferred.
3. Familiar with pharmacology and related basic knowledge, and able to design and implement mechanism research schemes based on the characteristics of drug action.
4. Familiar with the technical specifications of pharmacology, toxicology, and non-clinical research, able to formulate implementation plans for new drug development projects according to relevant technical requirements.
5. Responsible for project progress and problem-solving ability. Able to report interim research results and encountered problems in a timely manner, and propose methods to solve problems and follow-up research plans.
6. Possess a high sense of responsibility and team spirit, able to actively execute and cooperate with superior arrangements.
7. Good English reading, writing, and communication skills.
about the company.
A biotechnology company specializing in peptide research and development, the company focuses on the production and application of peptide-based products in the fields of healthcare and pharmaceuticals.
about the team.
A company that is open to accepting new ideas and suggestions is one that fosters a culture of innovation and collaboration. It welcomes creativity and encourages employees to share their insights and perspectives.
about the job.
1. Responsible for in vitro and in vivo pharmacological studies of new drug development, for drug efficacy evaluation during the new drug development process. This includes project initiation research, experimental protocol design, new method development and validation, result statistical analysis, and review of experimental reports.
2. Primarily responsible for the design of in vivo pharmacokinetic experimental protocols, participation in animal model establishment and validation, as well as drug evaluation protocol design.
3. Assist in solving difficult problems undertaken by all departments, providing solutions through literature research, consultation with internal and external experts, and supervising the successful resolution of issues.
...
skills and experience required.
1. Doctoral degree in biology, pharmacology, or pharmacy, with more than two years of relevant work experience.
2. Able to independently design PK schemes based on drug molecular characteristics, and interpret PK data to support molecular or dosing scheme optimization. Candidates with more than two years of DMPK experience in CRO or R&D pharmaceutical companies are preferred.
3. Familiar with pharmacology and related basic knowledge, and able to design and implement mechanism research schemes based on the characteristics of drug action.
4. Familiar with the technical specifications of pharmacology, toxicology, and non-clinical research, able to formulate implementation plans for new drug development projects according to relevant technical requirements.
5. Responsible for project progress and problem-solving ability. Able to report interim research results and encountered problems in a timely manner, and propose methods to solve problems and follow-up research plans.
6. Possess a high sense of responsibility and team spirit, able to actively execute and cooperate with superior arrangements.
7. Good English reading, writing, and communication skills.
See what comes ahead in the application process. Find out how we help you land that job.
Applying with us is easy. We will review your application and see if you are a good fit for the job and the company.
Our consultant will call you at a suitable time to discuss your application and further career aspirations.
If you’ve never worked with us before, we’ll need some basic additional pieces of information to confirm your eligibility for work.
Next, we just need to verify a few things - we’ll make the relevant compliance checks and keep you posted.
As part of the process in ensuring you’re perfect for the role, we’ll make contact with any relevant references you’ve provided.
Our expert team will either arrange an interview for the role you’ve applied for, or if they believe there’s a better opportunity, they’ll suggest alternative options too.
We’ll ensure that you’re fully prepared ahead of your interview and know exactly what to expect - good luck!
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