Provides clinical, regulatory, and compliance services to life sciences.
| Title |
|---|
| Pharmacovigilance Specialist, Submissions Full Time Hyderabad, Telangana, India · Hybrid |
| Freelance/Contract - Pharmacovigilance Specialist, Case Processing & QPPV Support Contract, Full Time Lund, Skane County, Sweden · Hybrid |
| Commissioning, Qualification & Validation Consultant II Full Time · $135K · 5+ YOE Troy, New York, United States · Hybrid |
| Associate Director, Regulatory Operations – Veeva Vault RIM BS Analyst Full Time, Contract · 5+ YOE Waltham, Massachusetts, United States · Remote |
| Director, Regulatory Affairs CMC Full Time · 10+ YOE Raleigh or Waltham · Hybrid |
| FSP Site Contract Specialist Full Time · 5+ YOE Raleigh, North Carolina, United States · Hybrid |
| Technical Procedure Writer Full Time · 3+ YOE Hyderabad, —, India · Hybrid |
| Project Manager (Contract - Irvine, CA) Full Time, Contract · 5+ YOE Irvine, California, United States · Hybrid |
| CEE Regulatory Affairs Specialist and Pharmacovigilance Officer Full Time · 2+ YOE Macedonia · Hybrid |
| Workday Technical Developer Full Time Hyderabad or United Kingdom · Hybrid |
| Accessioning Technician (Contract-Phoenix, AZ) Full Time Phoenix, Arizona, United States · Hybrid |
| Global Audit Coordinator Full Time Raleigh, North Carolina, United States · Remote |
| Met us at NIBRT? Start your career in Medical Information with ProPharma Full Time Dublin or Ireland · Hybrid |
| Information Specialist Full Time Raleigh, North Carolina, United States · Hybrid |
| Multilingual Medical Information Specialist Full Time Melbourne, Victoria, Australia · Hybrid |
| Multilingual Medical Information Specialist, Japan Full Time Tokyo, /, Japan · Hybrid |
| Multilingual Medical Information Specialist Full Time · 1+ YOE Tokyo, Tokyo, Japan · Onsite |
| Pharmacovigilance Scientist Full Time · 2+ YOE Hyderabad, Telangana, India · Remote |
| Virtual Pharmacovigilance Auditor Full Time Raleigh, North Carolina, United States · Remote |
| Freelance SCRA - 0.4 FTE - Portuguese Speaking Contract, Part Time · 5+ YOE London, England, United Kingdom · Hybrid |
| Instrument Connectivity and Qualification Engineer (Consultant) Full Time United States or Chicago · Hybrid |
| Senior Pharmacovigilance Manager, Benefit Risk Full Time · 7+ YOE Berlin, Berlin, Germany · Hybrid |
| Regulatory Safety Lead (MD) Full Time, Contract · 15+ YOE Raleigh, North Carolina, United States · Remote |
| Empower Integration Engineer (Labvantage) Full Time Raleigh, North Carolina, United States · Hybrid |
| Director, Regulatory Sciences Full Time · 7+ YOE Washington, District of Columbia, United States · Hybrid |
| Activities | Clinical research managementRegulatory compliance consultingPharmacovigilance servicesMedical information servicesR&D technology consulting |
| Headquarters | US |
| Industries | Life SciencesProfessional Services |
| Name | ProPharma |
| Employees | 2,500 |
| Type | Private |
| Subsidiaries | iSafetyDigital Lab ConsultingClinres FarmacijaOneSource RegulatoryRegulatory Compliance Associates |
| Tagline | Provides clinical, regulatory, and compliance services to life sciences. |
| Founded | 2,001 |
| Website | propharmagroup.com |
| Latest Funding Round | Private Equity |
| Latest Funding Year | 2,020 |
| Latest Funding Amount | 744,000,000 |
| Latest Investors | Odyssey Investment Partners |