
51 - 200 employees
🧬 Biotechnology
💊 Pharmaceuticals
Biotechnology • Pharmaceuticals
Praxis Precision Medicines, Inc. is a clinical-stage biopharmaceutical company translating insights from human genetics into the development of precision therapies for central nervous system (CNS) disorders, with a strong focus on genetic epilepsies and neuronal excitation–inhibition imbalance. The company uses genetics-driven target selection, translational tools, patient-guided development, and efficient clinical strategies to advance multiple clinical- and early-stage programs aimed at delivering high-impact treatments for patients with complex brain disorders.
🔥 0 minutes ago
Improve your chances of getting an interview by checking your resume score before you apply.

51 - 200 employees
🧬 Biotechnology
💊 Pharmaceuticals
Biotechnology • Pharmaceuticals
Praxis Precision Medicines, Inc. is a clinical-stage biopharmaceutical company translating insights from human genetics into the development of precision therapies for central nervous system (CNS) disorders, with a strong focus on genetic epilepsies and neuronal excitation–inhibition imbalance. The company uses genetics-driven target selection, translational tools, patient-guided development, and efficient clinical strategies to advance multiple clinical- and early-stage programs aimed at delivering high-impact treatments for patients with complex brain disorders.
• Implements all activities related to the preparation of defined medical and regulatory documents • Supports documents for regulatory submissions to US and global health authorities • Collaborates with cross-functional team members to ensure accurate and timely completion and delivery of high-quality documents • Supports clinical trial transparency and disclosures • Contributes to departmental development through editorial and review support for document templates
• Bachelor’s degree required within a scientific discipline • A minimum of 3 years of medical writing experience in Sponsor or CRO setting • AMWA certification preferred • Experience using medical writing systems and technologies including Veeva RIM • Knowledge of drug development, study conduct processes, ICH guidelines, and FDA/EU guidance or demonstrated success within a regulated industry environment
• Remote work options • Professional development opportunities • Diverse and inclusive work environment
Apply Now🕒 January 28
Medical Writer producing high-quality documents for regulatory and scientific reports at Criterion Edge. Collaborating with project teams to ensure clarity, accuracy, and adherence to deadlines.
🕒 December 3, 2025
Part-time mental health writers or actors needed for AI safety initiatives. Role involves creating and performing clinical scenarios with AI agents in mental health contexts.
🕒 July 7, 2025
Seeking a freelance medical writer for Healthcare Consultancy Group (HCG) projects in Publications and Medical Affairs.
🇺🇸 United States – Remote
💵 $90 - $130 / hour
⏳ Contract/Temporary
🟡 Mid-level
🟠 Senior
🏥📝 Medical Writer