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PrimeVigilance, an Ergomed company, was set up by former Pharmacovigilance Regulators in 2008. We have grown to become the leading Pharmacovigilance specialist company, delivering global solutions for both clinical safety and post-marketing pharmacovigilance, as well as medical information from our offices. Having successfully delivered Pharmacovigilance (PV) and Medical Information (MI) services for over 14 years, our experience enables us to offer a comprehensive, top quality, cost-effective, and innovative safety solution. Our flexible approach, tailor-made to work with clients, allows us to deliver the services that meet your clinical and post-marketing needs.From its operational hubs based in Europe, the USA, and Japan. PrimeVigilance manages a global Pharmacovigilance system with a choice of leading drug safety databases, stretching to more than 100 countries.• 900+ highly qualified professionals• Global leader in QPPV services• 24/7 multilingual call center• Choice of leading drug safety databases• Robotic Process Automation (RPA) expertise• Access to regulatory experts and key opinion leadersGLOBAL LIFE CYCLE MANAGEMENT SERVICES• PHARMACOVIGILANCE • PHARMACOEPIDEMIOLOGY & BENEFIT-RISK MANAGEMENT• AUDIT & INSPECTION• QUALITY MANAGEMENT• REGULATORY SCIENCE
Remote model
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Hires remotely from
33 countries
Hires remotely from
Live jobs
Medical Information Associate
Junior (1-2 years)
VP / Senior Director / Director Business Development
Expert & Leadership (>10 years)
Clinical Team Manager
Senior (5-10 years)
Centralized Monitor
Senior (5-10 years)
Quality Manager, Quality Assurance
Senior (5-10 years)
Senior Clinical Research Associate (West Coast based)
Senior (5-10 years)
Trial Master File Specialist (TMFS) II/Snr TMF - TMF and ALCOA principles experience required
Mid-level (2-5 years)
Senior Auditor, Quality Assurance (Pharmacovigilance Audit/GCP Audit experience required)
Senior (5-10 years)
Site Manager
Senior (5-10 years)
IT Project Manager
Senior (5-10 years)
Senior Clinical Research Associate (East Coast based)
Senior (5-10 years)
Business Development Director (Clinical Research), UK and Nordics
Expert & Leadership (>10 years)
Medical Writer III (Pharmacovigilance)
Senior (5-10 years)
CRA II
Mid-level (2-5 years)
Clinical Research Associate II / Senior CRA (Spanish, Portuguese & English fluency)
Mid-level (2-5 years)
Clinical Research Associate II / Senior CRA (French Speaking)
Mid-level (2-5 years)
Clinical Research Associate II / Senior CRA
Mid-level (2-5 years)
GMP Auditor (Freelance)
Senior (5-10 years)
Senior Pharmacovigilance Project Manager/PV Project Manager- Europe
Senior (5-10 years)
Senior Pharmacovigilance Project Manager- Europe
Senior (5-10 years)
Local Contact Person for Pharmacovigilance and Regulatory Affairs (Permanent or Contractor)
Senior (5-10 years)
Local Contact Person for Pharmacovigilance and Regulatory Affairs (Contractor position)
Senior (5-10 years)
Local Contact Person for Pharmacovigilance and Regulatory Affairs (Contractor)
Senior (5-10 years)
Director, Business and Process Optimization (Pharmacovigilance)
Expert & Leadership (>10 years)
Safety Systems Specialist
Senior (5-10 years)
Senior Benefit/Risk Associate
Senior (5-10 years)
Pharmacovigilance Officer (senior level position)
Senior (5-10 years)
Manager, Regulatory and PV Delivery
Senior (5-10 years)
Last 90 days vs. the 90 days before
Rolling 12 months
Peak month
Jul · 58roles
Avg / month
20.2 roles
Momentum
+97% QoQ
What people ask before applying to PrimeVigilance
PrimeVigilance currently has 28 open remote roles listed on Jobgether. Open any role from the list on this page to see the details and apply directly.
PrimeVigilance has 501–1,000 employees.
PrimeVigilance operates in Clinical Research (CRO).
PrimeVigilance was founded in 2008.
See which PrimeVigilance roles match your profile, requirement by requirement, before you send a single application.
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