Jobs No Experience No Matric Needed Jobs in Centurion Gauteng
Scientific / QA
Pharmacovigilance Physician - Centurion Salary Dependent On Experience And Qualification
Express Employment Professionals Sa - Midrand
Centurion
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 Safety reports, and RMPs is mandatory. Prior experience in supporting business development activities
share this job on whatsappRegulatory Affairs Scientist (pharma). Centurion. Up To R50k P/m Bonus. R40k To R50k P/m, Plus Bonus
Specialist Search RecruitmentCenturion
R40k to R50k p/m, plus bonus experienced regulatory affairs pharmacist team. You need at least TWO full years of regulatory affairs scientist scientist or regulatory affairs associate experience at a pharmaceutical company to apply. Ideally, you 2 full years of RA Scioentist or RA Associate experience at a pharma company to apply. Salary is negotiable influenced by your qualifications, your level of experience, and your number of years in a similar role.
Regulatory Project Manager Centurion
Specialist Search RecruitmentCenturion
R40k to R50k p/m, plus bonus experienced regulatory affairs pharmacist team. You need at least TWO full years of regulatory affairs scientist scientist or regulatory affairs associate experience at a pharmaceutical company to apply. Ideally, you 2 full years of RA Scioentist or RA Associate experience at a pharma company to apply. Salary is negotiable influenced by your qualifications, your level of experience, and your number of years in a similar role.
Pharmacovigilance Physician Centurion
Express Employment Professionals Sa - MidrandCenturion
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 Safety reports, and RMPs is mandatory. Prior experience in supporting business development activities
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