HGR Supervisor

该职位来源于猎聘

Job Purpose 工作目标

负责产品层面人类遗传资源申报及合规管理，确保相关临床项目按计划合规开展。

Responsible for the HGRAC submission and compliance management at the product level, ensuring clinical projects are carried out as planned and in compliance with HGRAC regulations.

Roles & Responsibility 主要职责

负责拟制产品层面的人遗申报策略和申报计划。 Responsible for developing the HGR application strategy and plan at the product level. 2.

负责审核临床项目研究方案、知情同意书、合同等相关材料。 Responsible for reviewing clinical project materials such as research protocols, informed consent forms, contracts, etc. 3.

负责人遗申报材料的准备、审核和递交。 Responsible for the preparation, review, and submission of HGR application materials. 4.

协同项目组做好所负责产品的人遗合规管理。 Collaborate with the project team to ensure compliance management of HGR for the assigned products.

Job Requirement 工作要求

医学、生物学、药学相关专业本科或以上学历。 Bachelor's degree or higher in medicine, biology, pharmacy, or a related field. 2.

有2年以上人遗申报管理经验，具备良好的项目管理能力。 At least 2 years of experience in HGR application management, with strong project management skills. 3.

良好的沟通交流能力和团队合作精神，工作认真细致。 Excellent communication skills and teamwork spirit. Attention to detail. 4.

良好的中英文表达能力。 Proficiency in both written and spoken English and Chinese.