Senior Medical Writer
ProPharmaHighlight
Summary
About the Role
About You
- Bachelor's degree or higher in a medical or scientific discipline.
- Minimum of 5 years of experience in writing clinical and/or regulatory documents for drugs, biologics, and/or medical devices.
- Advanced knowledge of clinical research principles and regulatory submission requirements.
- Exceptional project management skills and strong communication skills.
Benefits
- Opportunity to work in a collaborative and innovative environment.
- Commitment to diversity, equity, and inclusion.
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!