Senior PV Scientist United States - Remote

Location: This position may be performed remotely, but requires the flexibility and willingness to travel as needed. The Opportunity Reporting to the Head of Pharmacovigilance, the Associate Medical Director, PV Scientist supports the medical oversight, analysis, coding, interpretation, and reporting of pharmacovigilance data at Praxis. This role contributes to high-quality safety surveillance, signal detection, benefit-risk evaluation, and regulatory compliance across clinical development programs. As Praxis advances its pipeline and prepares for regulatory submissions, this position plays a critical role in strengthening U.S.-based pharmacovigilance footprint, enhancing vendor oversight, supporting implementation of evolving safety infrastructure, and ensuring inspection readiness. The Associate Medical Director, PV Scientist enables the PV Lead to focus on clinical safety strategy, regulatory submission activities, and labeling development by providing both strategic and operational support across safety activities. Primary Responsibilities Serve as the U.S.-facing PV leader, ensuring timely follow-up on safety actions across global teams and time zones. Proactively identify and resolve operational gaps before they become compliance risks. Own oversight of end-to-end PV service providers, including governance meetings, KPI monitoring, TMF documentation, and continuous process improvement. Ensure quality, timeliness, and regulatory compliance at all times. Contribute to the development and evolution of PV SOPs, safety management plans, and database migrations. Lead or support implementation of new safety tools (e.g., signal detection platforms, monitoring systems) to strengthen proactive surveillance. Support signal detection activities, literature review, aggregate report preparation, and safety governance meetings. Author signal assessments, benefit-risk evaluations, and health hazard evaluations with scientific rigor and clarity. Prepare and/or QC safety narratives, regulatory safety responses, IND/NDA/MAA components, and DSMB materials. Ensure TMF documentation is complete, accurate, and inspection ready. Maintain compliance with global safety reporting requirements. Collaborate with Clinical Operations, Regulatory, Medical Affairs, Commercial, and Quality to ensure aligned safety processes, including call center setup, partner safety data exchange, and commercialization readiness activities. Ensure safety data exchange complies with partner agreements. Author searches for strategies for regulatory queries and internal requests. Maintain rigorous documentation standards to support inspections and audits. Qualifications and Key Success Factors Nurse, Nurse Practitioner, Pharmacist, or Allied Health Professional. Minimum 3-5 years of experience in pharmacovigilance within the pharmaceutical/biotechnology industry. At least 1 year of clinical trial experience highly desirable. Experience with regulatory filings (INDs, NDAs, MAAs). Strong knowledge of FDA, EMA, ICH, and GVP pharmacovigilance regulations. Experience in individual case safety reporting (clinical and post-marketing), aggregate reporting, signal detection, risk management planning, regulatory inspections, and PV SOP development. Experience implementing safety databases and signal detection tools preferred. Familiarity with MedDRA and WHO-Drug coding. Excellent written and verbal communication skills. Key Success Factors at Praxis Ownership mindset: You act like the safety infrastructure is yours. You don’t wait for direction to solve problems. Operational rigor: You create clarity in ambiguity and ensure documentation withstands inspection scrutiny. Scientific judgment: You understand the difference between noise and signal and contribute meaningfully to benefit-risk discussions. Speed with precision: You move quickly without sacrificing quality. Cross-functional credibility: You build trust across Clinical, Regulatory, Medical Affairs, Commercial, and external partners. Builder mentality: You enjoy scaling systems, not just operating within them. Candid communicator: You raise risks early, directly, and constructively. The physical and mental requirements of our roles include but are not limited to regular use of a computer, devices or other office equipment, clear communication, and occasional movement. You'll need comfort with screen work, basic hand coordination, and focus. Reasonable accommodations may be made to enable individuals with disabilities to perform these functions. Praxis Precision Medicines is an equal opportunity employer. We are committed to providing opportunities to all qualified applicants without regard to race, religious creed, color, gender identity or expression, age, national origin, sexual orientation, disability, genetics, military service and veteran status, or any other characteristic protected by federal, state, or local laws. Praxis does not accept unsolicited submissions from recruitment agencies for open positions. We ask all recruitment agencies to refrain from contacting any Praxis employee regarding any position. Compensation and Benefits We offer a competitive total rewards package, including annualized base salary in the range of $136,000 - $156,000 USD. Final salary range may be modified commensurate with job level, education, and experience. Benefits include medical/dental/vision coverage, life insurance, AD&D, disability benefits, 401(k) matching up to 6%, stock incentives, ESPP, discretionary quarterly bonus, wellness benefit, generous PTO, paid holidays, and company-wide shutdowns. Company Overview Praxis Precision Medicines is a clinical-stage biopharmaceutical company translating genetic insights into therapies for CNS disorders. Our core values are Trust, Ownership, Curiosity, and Results. We are focused on diversity, equity, and inclusion and are an equal opportunity employer. #J-18808-Ljbffr Praxis Precision Medicines Inc.