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Manager, Regulatory and PV Delivery
Summary:
The Manager, Regulatory and PV Delivery is responsible for developing the strategy based on regulatory requirements and for driving regulatory and PV deliverables based on an established PV and regulatory plan. They actively assist senior management in securing new business by participating to BDMsEmployment Type: Full-time
Experience Level: Mid-Senior Level
Senior Pharmacovigilance Associate
Summary:
Performing activities in the scope of ICSR management unit within agreed extent and timeframe: Processing Individual Case Safety Reports (ICSRs) from all sources in compliance with applicable regulations, PrimeVigilance procedures and in accordance with client specific requirements and timelines PerEmployment Type: Full-time
Experience Level: Entry Level
Tags: Science Pharmaceuticals
Senior Pharmacovigilance Associate
Summary:
Performing activities in the scope of ICSR management unit within agreed extent and timeframe: Processing Individual Case Safety Reports (ICSRs) from all sources in compliance with applicable regulations, PrimeVigilance procedures and in accordance with client specific requirements and timelines PerEmployment Type: Full-time
Experience Level: Entry Level
Tags: Science Pharmaceuticals
Senior Pharmacovigilance Associate
Summary:
Performing activities in the scope of ICSR management unit within agreed extent and timeframe: Processing Individual Case Safety Reports (ICSRs) from all sources in compliance with applicable regulations, PrimeVigilance procedures and in accordance with client specific requirements and timelines PerEmployment Type: Full-time
Experience Level: Entry Level
Tags: Science Pharmaceuticals
Senior Pharmacovigilance Associate
Summary:
Performing activities in the scope of ICSR management unit within agreed extent and timeframe: Processing Individual Case Safety Reports (ICSRs) from all sources in compliance with applicable regulations, PrimeVigilance procedures and in accordance with client specific requirements and timelines PerEmployment Type: Full-time
Experience Level: Entry Level
Tags: Science Pharmaceuticals
Senior Pharmacovigilance Associate
Summary:
Performing activities in the scope of ICSR management unit within agreed extent and timeframe: Processing Individual Case Safety Reports (ICSRs) from all sources in compliance with applicable regulations, PrimeVigilance procedures and in accordance with client specific requirements and timelines PerEmployment Type: Full-time
Experience Level: Entry Level
Tags: Science Pharmaceuticals
Senior Pharmacovigilance Associate
Summary:
Performing activities in the scope of ICSR management unit within agreed extent and timeframe: Processing Individual Case Safety Reports (ICSRs) from all sources in compliance with applicable regulations, PrimeVigilance procedures and in accordance with client specific requirements and timelines PerEmployment Type: Full-time
Experience Level: Entry Level
Tags: Science Pharmaceuticals
EDC Developer (Medidata RAVE and Zelta v1.0)
Summary:
The EDC Developer within the ERGOMED Data Management (DM) department is responsible for all tasks linked to the building of the EDC application for complex projects. The EDC Developer represents a position under direction of the Director of Data Management, with oversight by the Project Data ManagerEmployment Type: Full-time
Experience Level: Mid-Senior Level
Tags: Research Pharmaceuticals
PV Project Manager
Summary:
Acting as the primary contact point for project-related matters 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 basEmployment Type: Full-time
Experience Level: Mid-Senior Level
PV Project Manager
Summary:
Acting as the primary contact point for project-related matters 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 basEmployment Type: Full-time
Experience Level: Mid-Senior Level
PV Project Manager
Summary:
Acting as the primary contact point for project-related matters 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 basEmployment Type: Full-time
Experience Level: Mid-Senior Level
Sales Development Account Manager
Summary:
The Sales Development Account Manager focuses on customer acquisition. This position is responsible for searching new potential clients-leads and reaching out to relevant prospects to bring new business opportunities. Generate and pre-qualify new leads by using appropriate company resources, programEmployment Type: Full-time
Experience Level: Mid-Senior Level
GCLP Auditor (Freelance - CAP/CLIA experience required)
Summary:
Planning, preparation, conduct, reporting and follow up of various types of GCLP audits including CAP/CLIA according to expected quality and timelines Executing audits based on a comprehensive understanding of all regulatory requirements and Good Clinical Laboratory Practice (GCLP). Performing GCLPEmployment Type: Full-time
Experience Level: Mid-Senior Level
Marketing Associate
Summary:
The Marketing Associate supports Ergomed’s global conference and event marketing activities, coordinating registrations, logistics, vendor communications, materials, invoicing, and event tracking. Working closely with internal teams and external partners, the role ensures events are delivered accuraEmployment Type: Full-time
Experience Level: Associate
Manager, Regulatory Registration and Compliance
Summary:
The Manager, Regulatory Registration and Compliance is responsible for developing the strategy based on regulatory requirements and for preparing/reviewing relevant Project Plans, joint operating procedures, and/or templates. They actively assist senior management in securing new business by particiEmployment Type: Full-time
Experience Level: Associate
Tags: Research Pharmaceuticals
PV Auditor - Freelance Position
Summary:
ADAMAS Consulting is looking for PV Auditor on a freelance basis to cover audits across USA and Canada. Both full and part time (0.6+ FTE) will be considered Planning, preparation, conduct, reporting and follow up (including CAPA plans) of various types of Pharmacovigilance (PV) audits according toEmployment Type: Full-time
Experience Level: Mid-Senior Level
Manager, Regulatory Registration and Compliance
Summary:
The Manager, Regulatory Registration and Compliance is responsible for developing the strategy based on regulatory requirements and for preparing/reviewing relevant Project Plans, joint operating procedures, and/or templates. They actively assist senior management in securing new business by particiEmployment Type: Full-time
Experience Level: Associate
Tags: Research Pharmaceuticals
Manager, Regulatory Registration and Compliance
Summary:
The Manager, Regulatory Registration and Compliance is responsible for developing the strategy based on regulatory requirements and for preparing/reviewing relevant Project Plans, joint operating procedures, and/or templates. They actively assist senior management in securing new business by particiEmployment Type: Full-time
Experience Level: Associate
Tags: Research Pharmaceuticals
Manager, Regulatory Registration and Compliance
Summary:
The Manager, Regulatory Registration and Compliance is responsible for developing the strategy based on regulatory requirements and for preparing/reviewing relevant Project Plans, joint operating procedures, and/or templates. They actively assist senior management in securing new business by particiEmployment Type: Full-time
Experience Level: Associate
Tags: Research Pharmaceuticals
Manager, Regulatory Registration and Compliance
Summary:
The Manager, Regulatory Registration and Compliance is responsible for developing the strategy based on regulatory requirements and for preparing/reviewing relevant Project Plans, joint operating procedures, and/or templates. They actively assist senior management in securing new business by particiEmployment Type: Full-time
Experience Level: Associate
Tags: Research Pharmaceuticals
Global People Services Associate (HR Ops_6 months - 1 yr experience)
Summary:
The Global People Services Associate acts as a support in a central hub for transactional HR activities. The Global People Services Associate provides efficient, consistent support to all employees and managers. Employee Support: Responding to HR-related questions from employees and managers (benefiEmployment Type: Full-time
Experience Level: Associate
GMP Auditor (Freelance)
Summary:
Planning, preparation, conduct, reporting and follow up of various types of GMP audits according to expected quality and timelines Executing audits based on a comprehensive understanding of all regulatory requirements and Good Manufacturing Practice (GMP) Performing GMP quality assurance projects onEmployment Type: Full-time
Experience Level: Mid-Senior Level