Job responsibilities
To receive and record the ADR/AEFI reports in the respective database. To receive and record aggregates safety reports (PSUR/PBRERs). To record the safety signal on medicines/vaccines in the prescribed database To conduct the aggregated analysis of Pharmacovigilance data using statistical methods and VigiLyze. To implement the Pharmacovigilance plan within the division To oversee the management of Pharmacovigilance data from Marketing Authorization Holders, Public Health Programs, Health Facilities, Industry, and academia; To recommend regulatory actions from data analysis for the safety and vigilance of medical products and health technologies, To monitor and evaluate data from pharmacovigilance active surveillance; To make follow up for the missing pharmacovigilance data from reporter.
Qualifications
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1
Bachelor’s Degree in Pharmacy
3 Years of relevant experience
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2
Master’s Degree in Pharmacy
1 Years of relevant experience
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3
Bachelor’s Degree in Pharmaceutical Sciences
3 Years of relevant experience
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4
master’s degree in biostatistics
1 Years of relevant experience
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5
Bachelor’s Degree in Biostatistics
3 Years of relevant experience
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6
Master’s Degree in Pharmaceutical Sciences
1 Years of relevant experience
Required competencies and key technical skills
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1Resource management skills
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2Analytical skills
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3Problem solving skills
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4Decision making skills
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5Time management skills
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6Risk management skills
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7Results oriented
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8Digital literacy skills
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9Fluency in Kinyarwanda, English and/or French. Knowledge of all is an added advantage.
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