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
License Experience: Planning experience and understanding of business processes 1-2 years' experience of HSEQR HSEQR Management 2 -3 years' experience in Construction related work. Technical/Core Training Excellent
License Experience: Planning experience and understanding of business processes 1-2 years' experience of HSEQR HSEQR Management 2 -3 years' experience in Construction related work. Technical/Core Training Excellent
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
QUALIFICATIONS / REQUIREMENTS / KNOWLEDGE / SKILLS / EXPERIENCE The Applicant must meet the following requirements: License Planning experience and understanding of business processes 3 years experience in SHEQR Management Management 3 years experience in Contractor Management and Project Management. Excellent knowledge of the IMS;
pharmacoepidemiology. Experience in clinical research and/or PV is preferred. Experience with leading or supporting agency enquiries and product quality issues. Experience in reviewing different aggregate report types Annual Safety reports and RMPs is mandatory. Prior experience in supporting business development activities meetings. Previous experience with authoring/reviewing PV procedures is preferred. Experience with PV processes timelines and changing priorities. Extensive experience in PV in the Pharmaceutical Industry, with a
pharmacoepidemiology. Experience in clinical research and/or PV is preferred. Experience with leading or supporting agency enquiries and product quality issues. Experience in reviewing different aggregate report types Annual Safety reports and RMPs is mandatory. Prior experience in supporting business development activities meetings. Previous experience with authoring/reviewing PV procedures is preferred. Experience with PV processes timelines and changing priorities. Extensive experience in PV in the Pharmaceutical Industry, with a
achieve their individual goals. Qualifications and Experience Bachelor's degree/ Advanced Diploma in Commerce be an added advantage. Relevant 6 - 8 years' experience in forensic investigation into white-collar crime Demonstrable experience of working with law enforcement agencies. Demonstrable experience of litigation
achieve their individual goals. Qualifications and Experience Bachelor's degree/ Advanced Diploma in Commerce be an added advantage. Relevant 6 - 8 years' experience in forensic investigation into white-collar crime Demonstrable experience of working with law enforcement agencies. Demonstrable experience of litigation
achieve their individual goals. Qualifications and Experience Bachelor's degree/ Advanced Diploma in Commerce be an added advantage. Relevant 6 - 8 years' experience in forensic investigation into white-collar crime Demonstrable experience of working with law enforcement agencies. Demonstrable experience of litigation