Safety analysis scientistLaboratory Corporation of America
Workplace: MetroManila, Manila
Salary: Agreement
Work form: Full time
Posting Date: 18/11/2025
Deadline: 12/03/2022
Job Overview:
The safety analysis scientist (SAS) is mainly responsible for core safety deliverables related to periodic and ad hoc aggregate reporting and safety monitoring of drug and vaccine products. The SAS will also support deliverables related to cross-functional or benefit-risk assessment teams, as required.
Perform aggregate analysis and case level review of medium to high complexity safety data, including data from clinical trials
Conduct literature and PV database searches
Organize and lead planning and strategy meetings, and perform project management activities for safety reports/deliverables.
Work closely with the safety physician and liaise with cross-functional stakeholders/teams
Author and contribute to various safety reports (or part of such reports) per approved strategy; perform quality review of such reports, as required
Participate, present analyses, and contribute to discussions in safety/benefit-risk review meetings.
Education/Qualifications:
Bachelor's degree in Health or Biomedical Science (6-8 years industry experience or equivalent)
Advanced Degree preferred in Health or Biomedical Science (4-6 years industry experience or equivalent)
Experience:
Authoring and review of periodic and adhoc safety reports (more than 5 years of experience required in safety or clinical documents such as PSURs, DSURs, ACOs, Clinical overviews, Clinical study reports or summaries); experience in signal detection/safety surveillance, risk management, and preparing responses to health authority requests preferred
Experience in safety analysis and writing for biologics, advanced therapy products or drug/vaccine products in development, preferred
Laboratory Corporation of America
The safety analysis scientist (SAS) is mainly responsible for core safety deliverables related to periodic and ad hoc aggregate reporting and safety monitoring of drug and vaccine products. The SAS will also support deliverables related to cross-functional or benefit-risk assessment teams, as required.
Perform aggregate analysis and case level review of medium to high complexity safety data, including data from clinical trials
Conduct literature and PV database searches
Organize and lead planning and strategy meetings, and perform project management activities for safety reports/deliverables.
Work closely with the safety physician and liaise with cross-functional stakeholders/teams
Author and contribute to various safety reports (or part of such reports) per approved strategy; perform quality review of such reports, as required
Participate, present analyses, and contribute to discussions in safety/benefit-risk review meetings.
Education/Qualifications:
Bachelor's degree in Health or Biomedical Science (6-8 years industry experience or equivalent)
Advanced Degree preferred in Health or Biomedical Science (4-6 years industry experience or equivalent)
Experience:
Authoring and review of periodic and adhoc safety reports (more than 5 years of experience required in safety or clinical documents such as PSURs, DSURs, ACOs, Clinical overviews, Clinical study reports or summaries); experience in signal detection/safety surveillance, risk management, and preparing responses to health authority requests preferred
Experience in safety analysis and writing for biologics, advanced therapy products or drug/vaccine products in development, preferred
Laboratory Corporation of America
Other Info
Manila City, Metro Manila
Permanent
Full-time
Permanent
Full-time
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Laboratory Corporation of America
About the company
Position Safety analysis scientist recruited by the company Laboratory Corporation of America at MetroManila, Manila, Joboko automatically collects the salary of , finds more jobs on Safety Analysis Scientist or Laboratory Corporation of America company in the links above