Director of Pathology in NCS
罗氏研发(中国)有限公司
- 公司规模:50-150人
- 公司性质:外资(欧美)
- 公司行业:制药/生物工程
职位信息
- 发布日期:2012-08-31
- 工作地点:上海
- 招聘人数:1
- 工作经验:五年以上
- 学历要求:博士
- 语言要求:英语熟练
- 职位类别:医药技术研发管理人员
职位描述
Description:
1. Act a toxicology and pathology leader for NCS of pRED China both inside & outside Roche
2. As a member of NCS management team, actively involve in setting up strategy and direction for the department;
3. Manage toxicology and pathology operation;
4. Establish a close collaboration with global NCS toxicology and pathology department;
5. Act as study or peer review pathologist for toxicology studies;
6. Act as discovery pathologist to support efficacy and animal model studies;
7. Be responsible for addressing nonclinical related pathology questions raised by peers or regulatory authorities for clinical trials and product registration worldwide;
8. Service as a champion in NCS to lead investigative toxicology and pathology studies as necessary to study the mechanism of toxicities identified in routine toxicology studies.
Qualification:
1.Education: DVM, Ph.D. or equivalent in veterinary pathology, ;
2.Board certification by the American or European Colleage of Vetrinary Pathologists (ACVP or ECVP) or equivalent3.Years of experience: at least 5 years of toxicologic pathology experience , ideally within pharma or biotech; training and experience in toxicology project support is highly desired;
4.Scientific Experience:
·Proven track record as a toxicologic pathologist with experience in supporting drug discovery and development projects;
·Experience with animal efficacy model development and evaluation;
·Experience of designing and executing complex toxicology program to support drug development projects is highly desired;
·Experience of representing preclinical safety department at cross functional drug R&D organization;
5.Knowledge:
·Broad background knowledge in pathology, toxicology, and safety assessment;
·Must be familiar with GLP regulations;
·Knowledge of new technologies in molecular pathology and image analysis is a plus;
6.Abilities:
·Ability to build trustful and effective working relationship with external and internal collaborators, such as CROs, universities, research institutes, and regulatory agencies;
·Be able to represent NCS of pRED China at international meetings or Roche internal global meeting;
7.Leadership competency:
·Proven track record of leading a group with different scientific background;
·Self-motivated with a strong ability to motivate others to deliver milestone within project timeline;
8.Skills:
·Good interpersonal and managerial skills
·Excellent English communication skills
1. Act a toxicology and pathology leader for NCS of pRED China both inside & outside Roche
2. As a member of NCS management team, actively involve in setting up strategy and direction for the department;
3. Manage toxicology and pathology operation;
4. Establish a close collaboration with global NCS toxicology and pathology department;
5. Act as study or peer review pathologist for toxicology studies;
6. Act as discovery pathologist to support efficacy and animal model studies;
7. Be responsible for addressing nonclinical related pathology questions raised by peers or regulatory authorities for clinical trials and product registration worldwide;
8. Service as a champion in NCS to lead investigative toxicology and pathology studies as necessary to study the mechanism of toxicities identified in routine toxicology studies.
Qualification:
1.Education: DVM, Ph.D. or equivalent in veterinary pathology, ;
2.Board certification by the American or European Colleage of Vetrinary Pathologists (ACVP or ECVP) or equivalent3.Years of experience: at least 5 years of toxicologic pathology experience , ideally within pharma or biotech; training and experience in toxicology project support is highly desired;
4.Scientific Experience:
·Proven track record as a toxicologic pathologist with experience in supporting drug discovery and development projects;
·Experience with animal efficacy model development and evaluation;
·Experience of designing and executing complex toxicology program to support drug development projects is highly desired;
·Experience of representing preclinical safety department at cross functional drug R&D organization;
5.Knowledge:
·Broad background knowledge in pathology, toxicology, and safety assessment;
·Must be familiar with GLP regulations;
·Knowledge of new technologies in molecular pathology and image analysis is a plus;
6.Abilities:
·Ability to build trustful and effective working relationship with external and internal collaborators, such as CROs, universities, research institutes, and regulatory agencies;
·Be able to represent NCS of pRED China at international meetings or Roche internal global meeting;
7.Leadership competency:
·Proven track record of leading a group with different scientific background;
·Self-motivated with a strong ability to motivate others to deliver milestone within project timeline;
8.Skills:
·Good interpersonal and managerial skills
·Excellent English communication skills
公司介绍
罗氏研发(中国)有限公司,位于上海张江高科技园区,是中国第一家由跨国制药企业独资拥有的药物研发中心,我们将通过尝试新的药物研发途径,为国内乃至国际市场提供具有临床差异性的药物。经过5年的发展,罗氏研发(中国)有限公司从早期药物发现工作起步,建立了从早期研究到早期开发全功能的药物研发业务部门,成为一个在中国拥有大批业内专家和广泛合作伙伴的药物研发组织。我们正在寻找药物研发行业内的领军人物加入我们,让我们共同创造医疗保健领域的美好明天。
联系方式
- 公司地址:上海张江高科技园区蔡伦路720弄5号
- 邮政编码:201203
- 联系人:HR
- 传真:(021)50790291