POSITION SUMMARY To responsible for timely reporting and processing of respective Serious Adverse Events (SAE), Adverse Event(AE) Serious and non-Serious Adverse Drug Reaction(SADR) and other medically related project information within agreed timeline to Health Authority and other Key Stakeholders. To responsible for document archiving, data tracking communication of respective safety reports in compliance with company’s and relevant regulator’s requirements. JOB FUNCTIONS/RESPONSIBILITYES The responsibilities of the (Senior) Pharmacovigilance Specialist may include, but are not limited to: Perform initial review of the adverse event perform seriousness and relatedness assessment and follow up SAE/AE/ADR/SADR queries to investigator sites or reporter(s) Liaise with the investigational site and or reporter regarding safety issue. Ensure accurate entry of safety data into the safety database or relevant system. May assist the team in create patient adverse event narratives, if appropriate Archive document related to entered safety data and other in accordance with regulatory requirement, respective SOPs and manuals. Communicate with relevant stakeholder (Health Authority, Site Staff) to clarify enquiry of entered data on the safety database May assist the Medical team to train member from other department on how to collect safety information for Spontaneous safety reporting of marketed product to the company. May assist the team member with safety case monitoring/ Screening activity on safety database. May attend the project team meeting and teleconference as needed.

C O M P E T E N C I E S/K E Y P E R F O R M AN C E I N D I C AT O R S

Number, Timeliness and quality of deliverable according to established directives Compliance with internal and external regulations and SOPs.

E D U C A T I O N , E X P E R I E N C E , S K I L L S AN D K N O W L E D G E R E Q U I R E M E N T S/ QUALIFICATIONS

Bachelor/Master or qualified in major of life science; Medical / Science background with relevant clinical experience Knowledge of medical Terminology Excellent communication skill Senior Drug Safety Associate - min 3 years’ experience as Drug Safety Associate or Related Global/Regional CRO/ pharmaceutical industry working experience EXPERIENCE & SKILLS Work experience in life sciences or medically related field, including biopharmaceutical clinical research experience obtained working on clinical trials in a biotech, pharmaceutical or CRO company

上班地址：黄陂南路838弄