Medical Writer

Job not on LinkedIn

🕒 June 30

🇺🇸 United States – Remote

⏳ Contract/Temporary

🟡 Mid-level

🟠 Senior

🏥📝 Medical Writer

👻 Ghost score 41%

What it means: how likely this posting is sitting open without active hiring.How to read it: 60% or higher means we think this is a ghost. Lower scores are less of a worry.How we score it: age, reposts, open roles vs team size, how fast jobs close, and whether pay is listed.Fine print: an estimate from public data, not a judgment of the company. Real jobs can score high, so treat it as a hint, not a fact.

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Praxis Precision Medicines, Inc.

WebsiteLinkedInAll Job Openings

51 - 200 employees

🏥 Healthcare

🧬 Biotechnology

💊 Pharmaceuticals

Healthcare • 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.

📋 Description

• 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

🎯 Requirements

• 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

🏖️ Benefits

• Remote work options • Professional development opportunities • Diverse and inclusive work environment