
1001 - 5000 employees
Founded 1997
đź’Ľ Consulting
🏥 Healthcare
📦 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.
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1001 - 5000 employees
Founded 1997
đź’Ľ Consulting
🏥 Healthcare
📦 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 • Perform activities within the ICSR management unit within agreed scope and timelines • Process Individual Case Safety Reports (ICSRs) from all sources in compliance with applicable regulations, company procedures, client requirements and timelines • Perform ICSR follow-up, SAE/SUSAR management, including unblinding, clinical trial reconciliation, protocol review and Safety Management Plan review • Perform clinical and partner reconciliation • Handle personal data protection and Product Quality Complaints • Interact with Quality Assurance and Medical Information • Perform MedDRA and WHO coding • Produce database outputs and reports, including data for monthly client reporting • Support workflow and resource management • Support pharmacovigilance processes related to ICSR management for PrimeVigilance and clients • Perform tasks assigned under SOPs to more junior positions, as applicable to senior colleagues • Support the RA & PV Network Department as needed • Act as 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 • Minimum 1 year of work experience in pharmacovigilance • Organization skills, including attention to detail and multitasking • Management skills, including time and issue management • English - advanced (spoken, written) • Advanced literacy (MS Office)
• 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 • Equal opportunities workplace • Human-centric environment • Employee experience, well-being and mental health emphasis • Work-life balance emphasis
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