Associate Director Preclinical Development

40-55万元/年

杭州市

刷新时间：2021-03-11

职位描述

Position
Responsibilities:

Provide input and support scientifically
sound strategies to drive therapeutic discovery, development and regulatory
decisions through preclinical development.

Enable the utilization of state-of-the-art
approaches to accelerate program progression and address critical program
issues.

Provide input for the design of
immunological and animal pahrmacology studies to achieve characterization and
lead optimization for immunotherapy products

Provide input for the design, conduct,
interpretation, and reporting of all toxicity and safety pharmacology studies
including resulting integrated risk assessments and mitigation strategies.

Address and resolve toxicological issues
arising in drug discovery and development programs, and adequately assess the
relevance of any toxicological findings to human safety.

Collaborate with the Clinical Development and
Regulatory Affairs functions to assure a well-defined IND/CTA submission
planning process for first in human studies and to ensure that the immunology,
pharmacology and toxicology program supports the timing and intent of clinical
trials.

Ability and willingness to work in cross-functional
teams with solid understanding of overall project planning and execution in the
setting of biopharmaceutical R&D.

Education/Experience:

Ph.D. or MS in Immunology, Biochemistry,
Pharmacology or Toxicology or related field.

A minimum of 3-5 years of experience in the
pharmaceutical industry with a proven track record of supporting drug discovery
and early development studies supporting therapeutic development.

Strong background in immunology is highly
preferred

History of success working in cross-functional
teams in drug development, with demonstrated 
accountability and achievement of results.

Reputation as a team player with a strong
track record and documented technical capabilities, drug development exposure
to link discovery research with product development in an overall preclinical
development strategy.

In depth understanding and working
knowledge of regulatory toxicology, GLPs, and US and International Regulatory
Guidelines.

Strong problem solver who is highly
organized with the ability to thrive and lead in a fast-paced innovative,
collaborative environment while remaining flexible, proactive, resourceful and
efficient.

其他要求

招聘人数：1人
汇报对象：COO&CBO
职能类别：其他研发职位

公司介绍

诗迈医药猎头是一家专业从事医药行业猎头服务的科技型企业，总部位于杭州，下属有上海、南京、广州、武汉等多家分公司，同时自主开发国内领先的猎头办公系统及医药人才网站，全面致力于海内外制药、生物、医疗、器械等行业线上线下人力资源整合。
公司与全国各地研发企业、生产企业及销售经营等企业及业内同行建立了良好互动平台，在欧、美、日等国家建立了海归引进平台，同时积极开展医药高等院校公益系列讲座，搭建了以人力、企业为主体的立体化咨询服务网，为医药企业人才队伍建设发挥了积极重要作用，为很多医药企业解决了高端人力之困。