Clinical Trial Liaison
Drive site-based trial execution, deliver protocol expertise, and manage risks to improve enrollment and retention.
Remote • United States
- Full Time
- $130,000 – $150,000
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Drive site-based trial execution, deliver protocol expertise, and manage risks to improve enrollment and retention.
Lead and develop global medical affairs to drive neuroscience product commercialization and cross-functional strategy.
Support monthly close, FP&A budgeting/forecasting, and financial reporting in a biotech-focused finance team.
Lead TMF program, ensuring inspection-ready documentation, compliance, and process improvements across trials.
Regulatory-compliant medical writing for clinical trials and submissions, leading documents and coordinating cross-functional teams.
Lead PV operations, oversee safety reporting, and drive pharmacovigilance strategies across global partners.
Lead analytical development activities, validating and troubleshooting methods within Praxis’ CMC, collaborating across teams to deliver scalable, GMP-compliant diagnostics for neurological medicines.
Quality Systems Manager responsible for designing, implementing, and maintaining GxP-compliant quality systems company-wide across Praxis programs.
Leads process chemistry for drug substance development from lab to commercial supply, collaborating across CMC and CRO/CDMO partners.
Deliver accurate, balanced, and compliant scientific exchange on disease state, clinical data, and the ulixacaltimide profile.
Lead field medical strategy and team execution for neurology in a pre-launch/launch setting across movement disorders.
Operationalize HUB, stand up PSP operations, and drive launch readiness with HIPAA compliance and data integrity.
Lead analytical development programs for small molecule drug substances and drug products, coordinating CDMO partners and ensuring cGMP compliance.
Strategic FP&A partner to Commercial guiding launch readiness and scaling to multi-billion-dollar revenue.
Design, develop, and maintain reliable, production-grade code across frontend, backend, and data layers with regulatory compliance focus.
Executive leadership for global API strategy across small molecules and oligonucleotides, driving CMC governance and scalable manufacturing innovations.
Oversees planning, tracking, coordinating, compiling, QC, submitting, and archiving regulatory submissions to U.S. and international agencies.
Senior regulatory strategist to lead global regulatory strategies, IND lifecycle management, and health authority interactions across clinical programs.