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上海赞荣医药科技有限公司

上海赞荣医药科技有限公司
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  • 单位性质:民营企业
  • 单位行业:科学研究和技术服务业
  • 单位规模:少于50人
  • 工作城市:浦东新区
  • 发布日期:2021-06-10 15:06
信息来源: 中南大学就业信息网 温馨提示:求职需提高谨慎,辨别信息真伪,勿上当受骗。

Biologist Project manager/ senior manager

Responsibilities:

(1)Propose differentiated(具有差异化的)drug discovery projects from biology perspective

(4)Demonstrated scientific expertise and reputation in targeted cancer therapy

(3)Industrial experience is not required (this is not a typo, indeed not required, we trust you can grow with company while contributing your previous research experience to the company.)

Qualifications:

(1)Demonstrated ability to think strategically, design and direct original research, draw sound conclusions

(4)PhD thesis and post-doc research in DNA damage response signaling or cancer signaling biomarker is must

(5)Industrial experience is not required (this is not a typo, indeed not required, we trust you can grow with company while contributing your previous research experience to the company.)


Translational science associate director/director/senior director

Responsibilities

1.Identify biomarker and develop relevant assays or animal models at CRO or internally.

2.Interact closely with preclinical and clinical departments, provide insight of the target biology, clinical benefit/outcome and trial design, combination therapy and patient stratification, etc.

3.Identify biomarker and develop relevant assays or animal models at CRO or internally.

4.Key contributor for target identification and target validation.

Qualifications:

1.Extensive experience in oncology. Familiar with target/diseases biology, pre-clinical and clinical development.

2.Postdoc training and experience in translational medicine/research is desirable.

3.Extensive experience in oncology. Familiar with target/diseases biology, pre-clinical and clinical development.



Project Manager of DMPK

Responsibilities:

1.Coordinate and oversee DMPK CROs in terms of study request, data quality, onsite inspection and other related activities.

4.Support Pre-IND and IND filing package preparation.

5.Lead or coach CRO in trouble shooting and development of new DMPK assays as required.

Qualifications:

1.In vitro ADME hands-on experience preferred.

2.0-2 years of relevant drug discovery experience in a pharmaceutical or biotechnology company.

3.In vitro ADME hands-on experience preferred.

4.Good interpersonal communication skills; good oral and written English.

5.Enthusiasm for in-depth DMPK knowledge and related cutting-edge technologies.