End-to-end bespoke solutions that de-risk & accelerate our partners' and sponsors' drug and device development programs
Raleigh, North Carolina
At ProPharma, we help pharmaceutical, biotechnology, and medical device companies bring life-changing therapies to market. From early development through clinical, regulatory approval, and commercialization, we provide expert guidance to navigate complex challenges and accelerate success. Our mission is simple: improving patient health and safety by delivering the highest-quality regulatory, compliance, clinical research, pharmacovigilance, and medical information services throughout the entire product lifecycle. With over 20 years of expertise in regulatory sciences, clinical research solutions, quality & compliance, pharmacovigilance, medical information, and R&D technology, ProPharma partners with clients across the complete product lifecycle through an advise-build-operate model. Our end-to-end suite of consulting solutions de-risks and accelerates high-profile drug and device programs, ultimately improving patient health and safety. Discover how ProPharma can help you inspire the future of science!
Hybrid · Canada
The Medical Information Specialist responds to unsolicited medical and safety inquiries from healthcare professionals and consumers while ensuring accurate documentation of adverse events. They maintain quality standards by performing checks on inquiries and adhering to regulatory requirements and internal SOPs.