about the company. A top-tier domestic pharmaceutical company.
...
about the job.
Pharmacology and Efficacy Studies:
Lead the selection and development of pharmacology and efficacy models for Endocrinology and Metabolism drug projects.
Utilize internal and external resources to design relevant in vivo experiments based on the project’s development stage to support R&D decision-making.
Collaborate with project leaders to track experiment progress and interpret data.
Target Biology and Translational Research:
Quickly familiarize with and master the biological mechanisms of project targets and required translational research plans.
Propose and develop methods and feasible implementation plans for preclinical in vivo mechanism studies.
Competitive Intelligence Tracking:
Regularly track competitive information for ongoing projects.
Summarize and update relevant clinical or preclinical progress to provide important reference points for project team decisions.
Project Management and Internal Resource Coordination:
Manage R&D outsourcing activities for relevant projects.
Coordinate and communicate with internal platform resources to ensure experimental plans can be smoothly executed.
skills and experience required.
Ph.D. or MD/Ph.D. in Endocrinology and Metabolism, Translational Medicine, Pharmacology, or a related field. Advanced degrees in related disciplines may be considered with appropriate experience.
Experience: 10+ years of experience in Endocrinology and Metabolism and translational research, with at least 2 years in a leadership role within pharmaceutical or biotechnology industries.
Proven track record of leading translational research teams and managing complex projects.
Extensive experience with preclinical and clinical research methodologies.
Preferred with experience in precision medicine and personalized immunotherapy approaches.
Demonstrated expertise in pharmacology, in vivo models, and Endocrinology and Metabolism drug development.
show more
about the company. A top-tier domestic pharmaceutical company.
about the job.
Pharmacology and Efficacy Studies:
Lead the selection and development of pharmacology and efficacy models for Endocrinology and Metabolism drug projects.
Utilize internal and external resources to design relevant in vivo experiments based on the project’s development stage to support R&D decision-making.
Collaborate with project leaders to track experiment progress and interpret data.
Target Biology and Translational Research:
Quickly familiarize with and master the biological mechanisms of project targets and required translational research plans.
Propose and develop methods and feasible implementation plans for preclinical in vivo mechanism studies.
Competitive Intelligence Tracking:
Regularly track competitive information for ongoing projects.
Summarize and update relevant clinical or preclinical progress to provide important reference points for project team decisions.
Project Management and Internal Resource Coordination:
Manage R&D outsourcing activities for relevant projects.
Coordinate and communicate with internal platform resources to ensure experimental plans can be smoothly executed.
skills and experience required.
Ph.D. or MD/Ph.D. in Endocrinology and Metabolism, Translational Medicine, Pharmacology, or a related field. Advanced degrees in related disciplines may be considered with appropriate experience.
Experience: 10+ years of experience in Endocrinology and Metabolism and translational research, with at least 2 years in a leadership role within pharmaceutical or biotechnology industries.
Proven track record of leading translational research teams and managing complex projects.
Extensive experience with preclinical and clinical research methodologies.
Preferred with experience in precision medicine and personalized immunotherapy approaches.
Demonstrated expertise in pharmacology, in vivo models, and Endocrinology and Metabolism drug development.
the application process.
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apply with randstad.
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we'll give you a call.
Our consultant will call you at a suitable time to discuss your application and further career aspirations.
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getting you registered.
If you’ve never worked with us before, we’ll need some basic additional pieces of information to confirm your eligibility for work.
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compliance check.
Next, we just need to verify a few things - we’ll make the relevant compliance checks and keep you posted.
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reference and background check.
As part of the process in ensuring you’re perfect for the role, we’ll make contact with any relevant references you’ve provided.
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the perfect job for you.
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.
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the interview.
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start your new job.
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about the company.a clinical stage biopharmaceutical company dedicated to providing innovative therapeutic solutions to address unmet medical needs globallyabout the job.Responsible for China domestic drug registration and filing, formulating registration strategy, evaluating registration risks, establishing registration pathways, and successfully completing various registration tasks. Drafting and editing IND, NDA, and other types of filing documents, as
about the company.a clinical stage biopharmaceutical company dedicated to providing innovative therapeutic solutions to address unmet medical needs globallyabout the job.Responsible for China domestic drug registration and filing, formulating registration strategy, evaluating registration risks, establishing registration pathways, and successfully completing various registration tasks. Drafting and editing IND, NDA, and other types of filing documents, as
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