Praxis Precision Medicines

Praxis Precision Medicines

24 open rolesLast updated April 28, 2026 at 5:02 PM UTC

All open jobs at Praxis Precision Medicines

Browse the full live job inventory for Praxis Precision Medicines. This page is focused on current openings, while the overview tab highlights role groups and hiring patterns.

24 open positions
  • Senior PV Scientist

    Lead pharmacovigilance activities, safety data management, and regulatory compliance across US programs.

    • Remote • United States
    • Full Time
    • $136,000 – $156,000/year
    • Min. 3 YOE
  • Director, Commercial Compliance

    Lead the development and scaling of Praxis’s U.S. commercial compliance program, enabling high-integrity, patient-centric commercialization while supporting business agility.

    • Remote • United States
    • Full Time
    • $200,000 – $225,000/year
    • Min. 5 YOE
  • Senior Clinical Trial Manager (CTM)

    Oversees end-to-end clinical trial management, cross-functional coordination, and regulatory submissions to deliver on time and within budget.

    • Remote • United States
    • Full Time
    • $168,000 – $188,000/year
    • Min. 5 YOE
  • Associate Director, Data Management

    Lead data management oversight and external vendors across studies, ensuring quality and regulatory compliance.

    • Remote • United States
    • Full Time
    • $166,000 – $188,000/year
    • Min. 5 YOE
  • Statistical Data Scientist

    Senior data scientist leads development and automation of analytical pipelines and statistical models for regulatory submissions.

    • Remote • United States
    • Full Time
    • $180,000 – $200,000/year
    • Min. 8 YOE
  • Senior Director, Medical Affairs, Neurology/CNS

    Lead Neurology Medical Affairs strategy across late-stage to post-marketing, engaging KOLs and patient advocacy groups.

    • Remote • United States
    • Full Time
    • $275,000 – $335,000/year
    • Min. 10 YOE
  • Senior Director, Quality Excellence (Systems & Technology)

    Strategic quality leader shaping and advancing enterprise QMS and GxP system lifecycle programs across clinical, manufacturing, and commercial operations.

    • Remote • United States
    • Full Time
    • $230,000 – $250,000/year
    • Min. 15 YOE
  • Clinical Trial Liaison

    Drive high-quality trial execution by partnering with clinical sites, delivering protocol expertise, and mitigating recruitment/retention risks.

    • Remote • United States
    • Full Time
    • $130,000 – $150,000/year
  • Head of Global Medical Affairs

    Leads medical affairs, builds a global team, and drives neuroscience strategy and commercialization.

    • Remote • United States
    • Full Time
    • $310,000 – $360,000/year
    • Min. 15 YOE
  • Senior Accountant

    Senior Accountant supporting monthly close, FP&A budgeting/forecasting, and cross-functional analysis to scale Praxis.

    • Remote • United States
    • Full Time
    • $85,000 – $105,000/year
    • Min. 3 YOE
  • TMF Operations Lead

    TMF operations lead ensuring accuracy, compliance, and inspection readiness across trial documentation.

    • Remote • United States
    • Full Time
    • $95,000 – $118,000/year
    • Min. 5 YOE
  • Senior Medical Writer - US

    Medical writing lead for regulatory documents supporting clinical trials and regulatory submissions.

    • Remote • United States
    • Full Time
    • $130,000 – $150,000/year
    • Min. 4 YOE
  • Principal Scientist, Analytical Development

    Lead analytical development activities across method development, validation and GMP testing for CMC pipeline in a global network.

    • Remote • United States
    • Full Time
    • $162,000 – $182,000/year
    • Min. 5 YOE
  • Quality Systems Manager

    Responsible for designing, implementing, and maintaining GxP quality systems across Praxis programs to support regulatory compliance and commercialization.

    • Remote • United States
    • Full Time
    • $124,000 – $144,000/year
    • Min. 5 YOE
  • Director, Process Chemistry

    Lead process chemistry development across small molecule programs, delivering scalable drug substance for clinical and commercial supply.

    • Remote • United States
    • Full Time
    • $210,000 – $230,000/year
    • Min. 12 YOE
  • Medical Science Liaison - Movement Disorders

    Communicates disease-state data and emerging CNS research to healthcare professionals to support medical strategy and readiness.

    • Remote • United States
    • Full Time
    • $145,000 – $175,000/year
    • Min. 5 YOE
  • Senior Medical Science Liaison - Movement Disorders

    Senior scientific leader leads MSL team, shaping field strategy and cross-functional execution in movement disorders.

    • Remote • United States
    • Full Time
    • $190,000 – $225,000/year
  • Lead, PSP Operations

    Operationalizes HUB and PSP, building workflows, training, and quality controls for launch.

    • Remote • United States
    • Full Time
    • $180,000 – $200,000/year
    • Min. 7 YOE
  • Senior Manager, Analytical Development

    Lead analytical development activities for small molecule substances and products within CDMO network, ensuring compliant data and collaborative execution.

    • Remote • United States
    • Full Time
    • $140,000 – $160,000/year
    • Min. 10 YOE
  • Director, Commercial FP&A

    Lead FP&A for commercial organization, building forecasting and ROI analyses to enable scaling toward multi-billion-dollar revenue.

    • Remote • United States
    • Full Time
    • $200,000 – $220,000/year
    • Min. 12 YOE
  • Software Engineer, Consultant

    Describes design, development, and deployment of production-grade software across frontend, backend, and data layers within eDiary and clinical data platforms.

    • Remote • Brazil
    • Full Time
    • Min. 3 YOE
  • Executive Director, Process Chemistry

    Owns and drives global API strategy across Praxis’ portfolio, aligning regulatory, manufacturing and CMC plans to accelerate timelines.

    • Remote • United States
    • Full Time
    • $280,000 – $306,000/year
    • Min. 12 YOE
  • Senior Regulatory Submissions, Manager

    Oversees planning, tracking, coordinating, compiling, QC, submitting and archiving regulatory submissions to U.S. and international agencies.

    • Remote • United States
    • Full Time
    • $120,000 – $140,000/year
    • Min. 7 YOE
  • Sr Manager / AD, Regulatory Strategy

    Strategic regulatory leadership coordinating global submissions and lifecycle planning for INDs, CTAs, and NDAs across multiple programs.

    • Remote • United States
    • Full Time
    • $160,000 – $180,000/year
    • Min. 6 YOE