regular Client meetings to present/discuss safety data received/reviewed. Advising the Client as requested relevant to PV or pharmacoepidemiology. Extensive experience of PV in the Pharmaceutical Industry, with focus aggregate report writing and risk management. Experience of orphan drug/rare diseases/biologics preferred safety preferred. Experience in clinical research and/or PV is preferred. Experience with leading or supporting agency inquiries, and product quality issues. Experience in reviewing different aggregate report types
equivalent
regular Client meetings to present/discuss safety data received/reviewed. Advising the Client as requested relevant to PV or pharmacoepidemiology. Extensive experience of PV in the Pharmaceutical Industry, with focus aggregate report writing and risk management. Experience of orphan drug/rare diseases/biologics preferred safety preferred. Experience in clinical research and/or PV is preferred. Experience with leading or supporting agency inquiries, and product quality issues. Experience in reviewing different aggregate report types
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Performing scientific functions including maintaining Data Tables and Statistical Tables. Generating and maintaining
Performing scientific functions including maintaining Data Tables and Statistical Tables. Generating and maintaining
Performing scientific functions including maintaining Data Tables and Statistical Tables. Generating and maintaining
Performing scientific functions including maintaining Data Tables and Statistical Tables. Generating and maintaining
Control/Assurance Manager. The ideal candidate will have experience working in a laboratory setting and possess a address any quality issues - Monitor and analyze data to identify trends and potential areas for improvement biology, etc.) - 5 years of experience in quality control/assurance roles - Experience working in a laboratory highly competitive salary for this role based on experience. Apply for this role today, contact Rebecca Grylls