1. 招聘职位
  2. 工作地点
  3. 招聘人数
  4. 发布日期
  5. 应聘

岗位职责

1.Direct and oversee the design and implementation of early stage clinical projects;
2.Ensure that all clinical programs have sound scientific and medical basis;
3.Design scientifically rigorous early stage clinical development programs for the various immune oncology programs;
4.Monitor study progress, leading the analyses and data evaluation process for progress reporting and presentations to internal senior management team and external advisory and other relative groups;
5.Prepare briefing and regulatory documents for regulatory agencies, such as Dossiers, INDs, and communicate with and responses to regulatory agencies about medical and other related issues.



任职要求

1.MD or equivalent, or medical scientist with sub-specialty training in oncology; 
2.Experience in clinical protocol design and implementation; experiences in I/O field required;
3.Three or more years of biotech or pharmaceutical industry related experience is required. Must demonstrate knowledge of clinical trial management, clinical and regulatory processes;
4.Excellent oral and written communication skills, as well as interpersonal skills.

岗位职责

 Direct and oversee the design and implementation of clinical projects developing transformative therapies for life-threatening hematologic malignancies;

 Ensure that all clinical programs have sound scientific and medical basis;

 Design scientifically rigorous clinical development programs for the various hematologic malignancies and or immune oncology programs;

 Monitor study progress, leading the analyses and data evaluation process for progress reporting and presentations to internal senior management team and external advisory and other relative groups;

 Prepare briefing and regulatory documents for regulatory agencies, such as Dossiers, INDs, and communicate with and responses to regulatory agencies about medical and other related issues.

任职要求

MD or equivalent, or medical scientist with sub-specialty training in hematologic oncology;

Experience in clinical protocol design and implementation; experiences in hematologic oncology or I/O field required;

Three or more years of biotech or pharmaceutical industry related experience is required. Must demonstrate knowledge of clinical trial management, clinical and regulatory processes;

Excellent oral and written communication skills, as well as interpersonal skills.

岗位职责

1、负责公司肿瘤领域药物临床试验,重点是方案制定、保证临床方案的设计依据于科学与医学。
2、负责与CDE审评专家、临床专家、其他临床研究人员和相关学科研究人员的沟通与交流;
3、负责相关项目的中国CFDA、 US FDA、EMA、和其他海外的临床和注册申报;

任职要求

1、临床医学肿瘤科硕士6年、博士3年或以上经验,本科必须是临床医学专业, 7-8年制(医学博士)优先考虑;

2、具有优秀的英语口语交流能力,能够有效推动工作效率、保障工作质量;
3、具有良好的团队组织及建设能力,

4、熟悉药物临床研究法规,熟悉肿瘤领域国内外临床研究发展与现状。

岗位职责

1、负责公司类风湿免疫科领域药物临床试验,重点是方案制定、保证临床方案的设计依据于科学与医学。
2、负责与CDE审评专家、临床专家、其他临床研究人员和相关学科研究人员的沟通与交流;
3、负责相关项目的中国CFDA、 US FDA、EMA、和其他海外的临床和注册申报;

任职要求

1、临床医学类风湿免疫科硕士6年、博士3年或以上经验,本科必须是临床医学专业, 7-8年制(医学博士)优先考虑;

2、具有优秀的英语口语交流能力,能够有效推动工作效率、保障工作质量;
3、具有良好的团队组织及建设能力,

4、熟悉药物临床研究法规,熟悉类风湿免疫科领域国内外临床研究发展与现状。

岗位职责

1、负责公司眼科领域药物临床试验,重点是方案制定、保证临床方案的设计依据于科学与医学。
2、负责与CDE审评专家、临床专家、其他临床研究人员和相关学科研究人员的沟通与交流;
3、负责相关项目的中国CFDA、 US FDA、EMA、和其他海外的临床和注册申报;

任职要求

1、临床医学眼科硕士6年、博士3年或以上经验,本科必须是临床医学专业, 7-8年制(医学博士)优先考虑;

2、具有优秀的英语口语交流能力,能够有效推动工作效率、保障工作质量;

3、具有良好的团队组织及建设能力;

4、熟悉药物临床研究法规,熟悉眼科领域国内外临床研究发展与现状。

应聘职位
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