ERGOMED
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.
Oncology • Neurology • Respiratory diseases • Orphan drugs • Metabolic diseases
Pharmacovigilance Project Manager - LCPPV responsibilities
6 hours ago
ERGOMED
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.
Oncology • Neurology • Respiratory diseases • Orphan drugs • Metabolic diseases
📋 Description
• Acting as the primary contact point for project-related matters and as a LCPPV • Managing client’s expectations to make sure the client is satisfied with services of PrimeVigilance, and that the work PrimeVigilance delivers meets, or even exceeds, the clients’ expectations • Preparing project scope and objectives based on the signed agreement between the client and PrimeVigilance • Project activities planning, including deadlines and interim milestones • Reporting for the client and the PrimeVigilance management, e.g., preparation of Monthly reports, serving as basis for invoicing
🎯 Requirements
• Proven track record of demonstrated Pharmacovigilance activities including processing and quality review of ICSRs • Writing or contributing to aggregate reports, literature screening, reconciliation, and preparation of SOPs • PV Project Management experience from ideally a service provider/CRO • Health Care Professional or Life Science Graduate • Be comfortable with communicating at senior levels within pharmaceutical organizations • Have good leadership qualities including skills in planning, mentoring, meeting facilitation, communication and problem solving • Must be Fluent in both English and German
🏖️ Benefits
• Training and career development opportunities internally • Strong emphasis on personal and professional growth • Friendly, supportive working environment • Opportunity to work with colleagues based all over the world, with English as the company language
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