Our client is one of the largest providers of information technology, consulting services and business-process solutions.
- Overall in-charge of day-to-day activities for sub-process in Pharmacovigilance/Drug Safety - Ensure Service Level Agreements are met by the whole of the Drug Safety group - Provide technical expertise to Pharmacovigilance/Drug Safety team. - Direct reports development in identifying training needs. - Address Performance Improvement Plans. - Manage and coordinate across Pharmacovigilance/Drug Safety sub-processes (Client specific) - Act as a gatekeeper for the changes requested to service or process (client specific) - Ensure compliance to SOPs. - Perform tasks/activities as communicated by the Project Manager. Documentation of all project related activities.
- Graduate/Postgraduate with a clinical degree or PG in science with 3-4 years relevant experience in Drug Development Services, Pharmacovigilance or Clinical Data Management - Knowledge of drug safety & clinical development and ICH/GCP principles - Knowledge of US and EU Pharmacovigilance regulatory - Excellent written and verbal communication skills and ability to present and critically discuss clinical data in both internal and external discussions.
- The chance to work in a dynamic, multicultural organization - Opportunity to work in a stable position - Well structured trainig plan from the first day - Competative salary and compensation package - Long-term opportunity - Chance to grow within the team
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