
5001 - 10000 employees
Founded 2001
đĽ Healthcare
đŚ Logistics
đ Manufacturing
đ° $8.6M Venture Round on 2020-10
Healthcare ⢠Logistics ⢠Manufacturing
ProPharma is a leading research consulting organization in the life sciences industry. The company specializes in providing custom solutions across the full product lifecycle, from early discovery to post-market monitoring. ProPharma's services include regulatory sciences, clinical research solutions, quality and compliance services, pharmacovigilance, medical information, and R&D technology. Known for its deep domain expertise, ProPharma assists clients in the pharmaceuticals, biotechnology, and medical device sectors with regulatory support, clinical development, and quality management. ProPharma's global team supports a wide range of therapeutic areas including oncology, cardiovascular, and rare diseases, among others, ensuring effective and efficient delivery of life-saving therapies.
đĄ We watch ProPharma's careers page
Every hour
how often we check
12
roles posted in the last 30 days
About 30 days
usual time to fill a role
38
roles closed in the last year
Selected: đ Date Added.
đ 3 days ago
Pharmacovigilance Specialist processing adverse-event cases for ProPharmaâs biotech, medical-device, and pharmaceutical clients. Coding MedDRA cases, preparing narratives, and supporting global safety compliance.
đ United Kingdom, Serbia, +2 more countries â Remote
đ° $8.6M Venture Round on 2020-10
â° Full Time
đ˘ Junior
đĄ Mid-level
đ§Ş Clinical Research
đŹđ§ UK Skilled Worker Visa Sponsor
đť Ghost score 10%
đ 3 days ago
Senior Pharmacovigilance Manager leading QPPV/LPPV services and PV teams for ProPharmaâs pharmaceutical, biotech, and medical-device clients. Overseeing regulatory compliance, client delivery, budgets, training, and audits.
đ Germany, Netherlands, +1 more countries â Remote
đ° $8.6M Venture Round on 2020-10
â° Full Time
đ Senior
đ§Ş Clinical Research
đť Ghost score 10%
đ 4 days ago
French-English Medical Information Specialist responding to drug safety enquiries for ProPharmaâs pharmaceutical, biotech, and medical device clients. Documenting adverse events and delivering compliant medical information remotely.
đ Serbia, United Kingdom â Remote
đ° $8.6M Venture Round on 2020-10
â° Full Time
âŞď¸ Entry-level
⨠French
đť Ghost score 10%
đŁď¸đŤđˇ French Required
đ 4 days ago
GVP/GCP Auditor supporting ProPharmaâs biotech, medical-device, and pharmaceutical clients. Managing audits, QMS, QA oversight, and regulatory compliance projects.
đ Japan, Australia â Remote
đ° $8.6M Venture Round on 2020-10
â° Full Time
đ´ Lead
đ§ QA Engineer (Quality Assurance)
đť Ghost score 10%
đŁď¸đŻđľ Japanese Required
đ October 23
Medical Information Specialist responding to German-English drug safety and product inquiries. Supporting pharmaceutical, biotech, and medical device companies with compliant medical information services.
đ Serbia, United Kingdom, +1 more countries â Remote
đ° $8.6M Venture Round on 2020-10
â° Full Time
âŞď¸ Entry-level
⨠German
đť Ghost score 10%
đŁď¸đŠđŞ German Required
đ October 20
Medical Information Specialist responding to medical and safety inquiries for ProPharma pharmaceutical clients. Documenting adverse events, product complaints, and regulatory information accurately.
đ United States, Canada â Remote
đ° $8.6M Venture Round on 2020-10
â° Full Time
đĄ Mid-level
đ Senior
đŚ H1B Visa Sponsor
đť Ghost score 10%
đ October 16
Principal Consultant leading product lifecycle integration projects for ProPharmaâs biotech, medical device, and pharmaceutical clients. Managing cross-functional teams, governance, budgets, supply, risks, and regulatory compliance.
đ Netherlands, Sweden, +4 more countries â Remote
đ° $8.6M Venture Round on 2020-10
â° Full Time
đ´ Lead
đŞ Product Specialist
đť Ghost score 10%
đ September 28
Quality assurance consultant supporting GxP compliance, audits, QMS, and regulatory projects for ProPharmaâs pharmaceutical, biotech, and medical-device clients. Advising clients on GMP issues, CAPA, and quality systems.
đ Sweden, Croatia â Remote
đ° $8.6M Venture Round on 2020-10
â° Full Time
đĄ Mid-level
đ Senior
đ§ QA Engineer (Quality Assurance)
đť Ghost score 12%
đŁď¸đ¸đŞ Swedish Required
đ September 22
Senior pharmacovigilance specialist managing ICSR, periodic, xEVMPD, and regulatory intelligence submissions. Supporting ProPharmaâs biotech, medical device, and pharmaceutical clients.
đ United States, Serbia, +2 more countries â Remote
đ° $8.6M Venture Round on 2020-10
â° Full Time
đ Senior
đ Compliance
đŚ H1B Visa Sponsor
đť Ghost score 14%