招聘岗位: 放射性药物研发总监/经理
工作职责:
1. 负责正电子放射性药品临床前研究项目的实验设计与执行,以及进行相关文献的查阅及整理;
2. 能够对正电子放射性药物领域的最新技术积极地提出建议、进行探索与实施工作;
3. 负责正电子放射性药物平台的建设与维护工作;
4. 负责正电子放射性药品的注册申报工作;
5. 协调CRO 和其他合作单位的研发合作项目;
6. 按照GMP/GLP 要求进行药品生产质量管理与检验。
任职资格:
1. 有机化学、药物化学、分析化学、放射药理学等相关专业博士学历;
2. 3-5 年以上放射性同位素合成、纯化和标记工作及其动物研究和药理学研究相关工作经验;
3. 熟悉中美放射性药品管理和注册法规;
4. 拥有GMP/GLP 相关工作经验;
5. 熟悉HPLC、TLC 等仪器原理与操作;
6. 有与多领域工作小组合作及与CRO 机构合作的经验;
7. 优秀的研发工作领导与管理能力;
8. 优秀的沟通与人际交流能力;
9. 中英文写作与口语熟练。
Position: R&D Director/Manager, PET radiopharmaceutical
Responsibilities:
1. Design and perform research in preclinical development studies of PET radiopharmaceuticals;
2. Actively propose, explore, and implement relevant new technology in the field of PET radiopharmaceutical development;
3. Establish and maintain state--‐of-the--art R&D platform for PET radiopharmaceutical;
4. Lead the drug registration process in both China and United States;
5. Supervise and coordinate R&D activities conducted at CROs and other research collaborators;
6. Conduct quality control based on GMP/GLP requirements.
Qualifications:
1. Doctoral degree in Organic Chemistry, Medicinal Chemistry, Analytic Chemistry, Radiopharmacology or a relevant scientific discipline
2. Minimum 3--‐5 years’ experience in synthesis, purification, labeling, animal studies, and pharmacological studies of radiopharmaceuticals;
3. Be Familiar with regulations and policies of radiopharmaceuticals in both China and United States;
4. Be Familiar with GMP and GLP requirements;
5. Be Familiar with HPLC and TLC technology desired;
6. Experience with working with multiple disciplinary teams and CROs;
7. Excellent leadership and management skills;
8. Strong communication and interpersonal skills;
9. Must be fluent in Chinese and English, both written and spoken. |