崗位職責(zé):
Regulatory Compliance
?Responsible for data collection, processing, documentation, reporting and follow-up of required adverse events (AE) reports within required timeline and quality for assigned projects;
?Tracking and archiving all safety reports and documents;
?Ensure compliance of PV audit and inspection in routine job and periodically review and to track, take action and close audit finding;
?Notify line manager (LM) of significant issues in a timely manner.
Monitor and Manage Investigational and Marketed Products Safety
?Proactively review and evaluate the clinical implications of safety data from different source for assigned projects;
?Review protocols, IBs and all safety sections of clinical and/or regulatory submission documents;
?Draft, review SAE case follow up queries;
?Draft SUSAR notification letter;
?Responsible for regulatory submission for safety expedited report within required timeline and quality.
?Implement other safety monitor responsibilities assigned by LM;
任職要求:
?Bachelor Degree in Medicine/Master or PhD preferred
?Fluent written and spoken English and Chinese
?Computer Skill: Computer literacy, knowledge with
?Medical PV knowledge and experience required
?Good knowledge of ICH, FDA and EMA PV regulatory requirement
?Good problem solving skills, communication skills and ability to learn new knowledge
?Good player to work both with a team as well as independently
職位福利:股票期權(quán)、五險(xiǎn)一金、交通補(bǔ)助、餐補(bǔ)、通訊補(bǔ)助、帶薪年假、補(bǔ)充醫(yī)療保險(xiǎn)、定期體檢