ProPharma Group careers
72 open roles at ProPharma Group (Company) in Belgrade, Makati City, London. Read from its own careers site. Search and filter these.
ProPharma helps navigate the complexities of drug development and ensure patient health and safety throughout the product lifecycle. propharmagroup.com
- Drug Safety Assistant
- Clinical Project Specialist - Hybrid
- German Speaking Medical Information Specialist - Graduate Opportunity
- Freelance SCRA - IRE - 0.8FTE
- Registered Nurse-Clinical Trial-New Glasgow, Nova Scotia CAN
- Pharmcovigilance Case processing & Quality Product Complaint Specialist
- Principal Pharmacovigilance Specialist
- GMP Compliance and Quality Assurance Auditor and SOP Technical Writer.
- Medical Information Specialist (Nurse)
- Quality Specialist
- Principal Consultant - Product Lifecycle Management - Permanent position
- Compliance and Quality Assurance Consultant - Product Quality Complaints - Permanent role
- Principal Medical Writer (Device)
- Interim VP, Regulatory Affairs
- Quality Record Investigation Lead Consultant
- Quality Record Investigation Consultant
- PV Specialist, Case Processing
- Director, Business Development- Quality and Compliance
- Director, Promotional Review & Labeling Services
- Registered Nurse-Clinical Trial-Chandler, Arizona
- Sterility Assurance Senior Consultant
- Program Lead/Sterility Assurance Review Senior Consultant
- Environmental Monitoring Program Lead Consultant
- Contract Adult Nurse - Poland
- Senior Clinical Research Associate - Alzheimer's Disease
- Image Service Product Owner (Consultant)
- Senior Project Manager - Rare Disease
- Compliance and Quality Assurance Consultant - Permanent position
- Safety Specialist, Pharmacovigilance Case Processing
- Principal Medical Writer
- Senior Pharmacovigilance Client Account Manager, Client Services
- Pharmacovigilance Client Account Manager, Client Services
- Director, Medical Writing
- Contract Adult Nurse - Spain
- Senior Pharmacovigilance Specialist, Regulatory Intelligence and Submissions
- Pharmacovigilance Safety Surveillance Specialist
- Medical Information Assistant
- Quality Documentation Specialist
- Senior Clinical Lead
- Computer System Validation Engineer
- Director, Business Development (Regulatory Sciences)
- Regulatory Promotional Review Consultant
- Director, Business Development (Medical Information Services)
- Principal Medical Writer (Consultant)
- Cell & Gene Therapy SME - US
- Multilingual Medical Information Specialist - Korean/English
- Multilingual Medical Information Specialist, Japan
- Senior Pharmacovigilance Consultant, Alliance Management
- 12 month FTC- Spanish speaking Medical Information Specialist
- Spanish Speaking Medical Information Specialist - Graduate Opportunity