
1001 - 5000 employees
Founded 1997
đź Consulting
đĽ Healthcare
đŚ Logistics
Consulting ⢠Healthcare ⢠Logistics
ERGOMED is a global group providing specialized services to the biotechnology and pharmaceutical industries. It operates under different service lines, including Ergomed Clinical Research, PrimeVigilance, and ADAMAS Consulting, and is dedicated to providing full-service clinical research organization (CRO) capabilities. Focused on oncology, rare diseases, and complex trials, it also offers end-to-end pharmacovigilance and medical information services, as well as comprehensive GxP audits. Ergomed is committed to supporting drug development with a global presence in around 100 countries.
đĽ 3 hours ago
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1001 - 5000 employees
Founded 1997
đź Consulting
đĽ Healthcare
đŚ Logistics
Consulting ⢠Healthcare ⢠Logistics
ERGOMED is a global group providing specialized services to the biotechnology and pharmaceutical industries. It operates under different service lines, including Ergomed Clinical Research, PrimeVigilance, and ADAMAS Consulting, and is dedicated to providing full-service clinical research organization (CRO) capabilities. Focused on oncology, rare diseases, and complex trials, it also offers end-to-end pharmacovigilance and medical information services, as well as comprehensive GxP audits. Ergomed is committed to supporting drug development with a global presence in around 100 countries.
⢠Provide support to other activities undertaken by the project team on behalf of the client and the company ⢠Line manage assigned ICSR staff ⢠Create and maintain project-specific KPIs for contracted ICSR activities ⢠Optimize procedures, trainings and other actions to increase ICSR team efficiency ⢠Propose process changes to the ICSR Operational Lead ⢠Manage ICSR deviations with support from the ICSR Operational Lead ⢠Review trackers and timesheet data and ensure accuracy ⢠Participate in ICSR processing and second quality control of cases ⢠Support other departments as approved and instructed by the ICSR Operational Lead ⢠Act as the assigned team subject matter expert and support other SMEs ⢠Support the RA & PV Network Department as needed ⢠Act as the LCPPV for the specified country and PRLS for the designated language, as agreed with the line manager
⢠Life science graduate, pharmacy, nursing, other healthcare related qualification or experience in pharmacovigilance ⢠5-6 years of work experience in pharmacovigilance ⢠Minimum 3 years of work experience in a line manager role ⢠Excellent written and verbal communication skills ⢠Organization skills, including attention to details and multitasking ⢠Delegation skills ⢠Planning and time management skills ⢠Technical skills ⢠Team working skills ⢠Fluent English, spoken and written ⢠Advanced literacy in MS Office
⢠Flexible/remote work arrangements ⢠Supportive, collaborative and inclusive work culture ⢠Growth and professional development opportunities ⢠Opportunity to work with global teams and contribute to patient safety ⢠Passionate team of experts in clinical research, pharmacovigilance, and quality consulting
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