Jobs at ProPharma Group
ProPharma provides regulatory sciences, clinical research, quality and compliance, pharmacovigilance, medical information, FSP, and digital transformation services. It supports pharmaceutical, biotechnology, and medical device companies from development through commercialization, helping clients ma…
- Industry
- Biotech & Pharma, Healthcare & Health Tech, Consulting & IT Services
- Company size
- 1,001–5,000 employees
- Open roles
- 62
- Data Integrity Program Lead ConsultantRaleigh, NCFull-time · Hybrid, On-site—
- Project Coordinator, GoClinicalZagreb, CroatiaFull-time · Remote, Hybrid—
- Global Admin Coordinator - AuditHyderabad, IndiaFull-time · Hybrid—
- Pharmacovigilance Specialist, Case ProcessingBelgrade, Serbia + 2 moreFull-time · Hybrid—
- Pharmacovigilance Specialist, Case ProcessingBelgrade, Serbia + 2 moreFull-time · Hybrid—
- Senior Pharmacovigilance Manager, QPPV OfficeBerlin, GermanyFull-time · Hybrid, On-site—
- CEE Regulatory Affairs and Pharmacovigilance SpecialistBelgrade, SerbiaFull-time · Remote, Hybrid—
- French Speaking Medical Information Specialist - Graduate OpportunityUnited KingdomFull-time · Remote, Hybrid—
- Project Manager, GoClinicalDeerfield Beach, FLFull-time · Remote, Hybrid, On-site—
- GVP/GCP Auditor, Compliance & Quality Assurance (Japan)Tokyo, Japan + 1 moreFull-time · Remote, Hybrid—
- Clinical Project Specialist - HybridBelgrade, Serbia + 2 moreFull-time · Hybrid—
- German Speaking Medical Information Specialist - Graduate OpportunityUnited Kingdom + 1 moreFull-time · Remote, Hybrid—
- GMP Compliance and Quality Assurance Auditor and SOP Technical Writer.Raleigh, NCFull-time · Remote, Hybrid—
- Pharmcovigilance Case processing & Quality Product Complaint SpecialistStockholm, SwedenFull-time · Hybrid—
- Principal Consultant - Product Lifecycle Management - Permanent positionLeiden, Netherlands + 4 moreFull-time · Hybrid—
- Compliance and Quality Assurance Consultant - Product Quality Complaints - Permanent roleStockholm, Sweden + 2 moreFull-time · Remote, Hybrid—
- Quality Record Investigation Lead ConsultantRaleigh, NCFull-time · Hybrid, On-site—
- Quality Record Investigation ConsultantRaleigh, NCFull-time · Remote, Hybrid, On-site—
- Principal Medical Writer (Device)Chicago, ILFull-time · Hybrid—
- PV Specialist, Case ProcessingMakati City, PhilippinesFull-time · Hybrid—
- Director, Business Development- Quality and ComplianceBelgrade, Serbia + 7 moreFull-time · Remote, Hybrid—
- Senior Project Manager - Rare DiseaseChicago, ILFull-time · Remote, Hybrid—
- Image Service Product Owner (Consultant)Raleigh, NCFull-time · Remote, Hybrid—
- Compliance and Quality Assurance Consultant - Permanent positionStockholm, Sweden + 1 moreFull-time · Remote, Hybrid, On-site—
- Principal Medical WriterUnited StatesFull-time · Hybrid—
- Safety Specialist, Pharmacovigilance Case ProcessingSwedenFull-time · Hybrid, On-site—
- Pharmacovigilance Client Account Manager, Client ServicesUnited StatesFull-time · Remote, Hybrid—
- Senior Pharmacovigilance Client Account Manager, Client ServicesUnited StatesFull-time · Remote, Hybrid—
- Pharmacovigilance Safety Surveillance SpecialistMakati City, PhilippinesFull-time · Hybrid, On-site—
- Senior Pharmacovigilance Specialist, Regulatory Intelligence and SubmissionsBelgrade, SerbiaFull-time · Hybrid—
- Director, Business Development (Regulatory Sciences)United StatesFull-time · Remote, Hybrid—
- Cell & Gene Therapy SME - USUnited StatesFull-time · Hybrid—
- Principal Medical Writer (Consultant)United StatesFull-time · Hybrid—
- Director, Business Development (Medical Information Services)United StatesFull-time · Remote, Hybrid—
- Multilingual Medical Information Specialist - Korean/EnglishMelbourne, AustraliaFull-time · Remote, Hybrid—
- Registered Nurse-Clinical Trial-Alexandria, VAUnited StatesFull-time · Remote, Hybrid, On-site—
- Senior Pharmacovigilance Consultant, Alliance ManagementStockholm, Netherlands + 6 moreFull-time · Remote, Hybrid—
- Registered Nurse-Clinical Trial-Fairfax, VAUnited StatesFull-time · Remote, Hybrid, On-site—
- Study Coordinator - High Point, NCUnited StatesFull-time · Remote, Hybrid, On-site—
- Research AssistantUnited StatesFull-time · Remote, Hybrid, On-site—
- Medical Information WriterIndiaFull-time · Remote, Hybrid—
- Computer System Validation EngineerBelgrade, SerbiaFull-time · Hybrid—
- GVP/GCP Auditor, Compliance & Quality Assurance – Japan—Full-time · Hybrid—
- Director, Business Development (CRO & FSP)United StatesFull-time · Remote, Hybrid—
- IT Access, Automation, and System AdministratorUnited StatesFull-time · Remote, Hybrid—
- Met us at NIBRT? Start your career in Medical Information with ProPharmaIrelandFull-time · Remote, Hybrid—
- Multilingual Medical Information Specialist, JapanTokyo, JapanFull-time · Remote, Hybrid—
- VP/Sr. VP of Advertising & Promotional ReviewUnited StatesFull-time · Remote, Hybrid—
See all 62 ProPharma Group roles
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