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
Control/Assurance Manager. The ideal candidate will have experience working in a laboratory setting and possess a standards - Coordinate with production teams to address any quality issues - Monitor and analyze data to identify 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 will put your CV on file and contact you regarding any future vacancies that arise. See Description See
Control/Assurance Manager. The ideal candidate will have experience working in a laboratory setting and possess a standards - Coordinate with production teams to address any quality issues - Monitor and analyze data to identify 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 will put your CV on file and contact you regarding any future vacancies that arise. See Description See
affairs scientist or regulatory affairs associate experience at a pharmaceutical company to apply. Ideally exposure and training to the docuBridge software. Any relevant tertiary qualification is sufficient. BSc 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.
affairs scientist or regulatory affairs associate experience at a pharmaceutical company to apply. Ideally exposure and training to the docuBridge software. Any relevant tertiary qualification is sufficient. BSc 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.
affairs scientist or regulatory affairs associate experience at a pharmaceutical company to apply. Ideally exposure and training to the docuBridge software. Any relevant tertiary qualification is sufficient. BSc 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.
affairs scientist or regulatory affairs associate experience at a pharmaceutical company to apply. Ideally exposure and training to the docuBridge software. Any relevant tertiary qualification is sufficient. BSc 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.
Risk Management: Identify, mitigate, and resolve any risks or issues related to remuneration practices Remuneration Practitioner (GRP) certification. 8 years ‘experience in Human Resource Management in specific Remuneration
Risk Management: Identify, mitigate, and resolve any risks or issues related to remuneration practices Remuneration Practitioner (GRP) certification. 8 years ‘experience in Human Resource Management in specific Remuneration
to 8 Years experience in laboratory environment