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HomeCompaniesPraxis Precision Medicines, Inc.Senior PV Scientist

Senior PV Scientist

Praxis Precision Medicines, Inc. · United States - Remote · Remote · Active · Greenhouse

Job facts

FieldValue
CompanyPraxis Precision Medicines, Inc.
TitleSenior PV Scientist
Normalized title-
Department / teamPharmacovigilance (PV)
LocationUnited States
Work modelRemote / Remote
Employment type-
Salary-
Statusactive
ATS providerGreenhouse
Posted / first seen2026-03-12 / 2026-05-29
Changed / last seen2026-05-29 / 2026-06-06

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PageWhat it containsOpen
Company jobsActive postings from Praxis Precision Medicines, Inc..Open
Company breakdownsRole, location, ATS, and work model facets for this company.Open
ATS provider jobsActive postings observed through Greenhouse.Open
Provider filtered searchThe same provider as a filtered job collection.Open
Department jobsActive postings in Pharmacovigilance (PV).Open
Work model jobsActive Remote postings.Open
Lifecycle eventsOpen, update, close, and reopen events for this posting.Open
Original postingCanonical source or apply URL captured from the ATS.Open

Linked records

CompanyPraxis Precision Medicines, Inc.
Sourceb8297d7e-52b9-46e1-841b-fcceb434fb6b
ATS providerGreenhouse

Description

Location: This position may be performed remotely, but requires the flexibility and willingness to travel as needed. The Opportunity 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 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. Annualized Base Salary $136,000 — $156,000 USD Company Overview Praxis Precision Medicines is a clinical-stage biopharmaceutical company translating genetic insights into the development of therapies for central nervous system disorders characterized by neuronal imbalance. At Praxis we share a common vision of reshaping the human condition into a more freeing and fulfilled existence by developing high impact medicines for patients and families affected by and living with complex brain disorders. Our core Values of Trust , Ownership , Curiosity and Results are foundational to every aspect of our business and are exemplified by each and every one of our team members. Diversity, Equity & Inclusion Guided by our core values, at Praxis Precision Medicines, Inc. we continue to DARE FOR MORE ® to advance, promote, and champion diversity, equity, and inclusion by encouraging individuals to bring their authentic selves and perspectives to work each day. We are an equal opportunity employer and 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. Attention: Job Scam Alert Praxis has recently become aware of fraudulent job recruitment postings from individuals claiming to represent Praxis. These postings seek financial information in connection with fraudulent opportunities for employment. If you suspect any fraudulent activity or misrepresentation in connection with a Praxis job opportunity, please report it to [email protected] . 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. All unsolicited resumes submitted by recruitment agencies to any Praxis employee in any form or method will be deemed to be the property of Praxis, and Praxis explicitly reserves the right to hire those candidate(s) without any financial obligation to the recruitment agency.

Full job record

Job IDc81efdb28b0852772afbdac2f3c2894a08c2eded
Org ID772627ef-6296-4c10-b894-175088324fbd
Source IDb8297d7e-52b9-46e1-841b-fcceb434fb6b
Board IDb8297d7e-52b9-46e1-841b-fcceb434fb6b
Providergreenhouse
Provider Job Key5148397008
TitleSenior PV Scientist
Normalized Title
Statusactive
Activeyes
Location TextUnited States - Remote
DepartmentPharmacovigilance (PV)
Team
Employment Type
Workplace Typeremote
Remote Policyremote
CountryUnited States
Region
City
Salary Raw
Salary Min
Salary Max
Salary Currency
Salary Period
Source URLhttps://job-boards.greenhouse.io/praxisprecisionmedicines/jobs/5148397008
Apply URLhttps://job-boards.greenhouse.io/praxisprecisionmedicines/jobs/5148397008
First Seen At2026-05-29 23:01:55Z
Last Seen At2026-06-06 07:34:51Z
Last Checked At2026-06-06 07:34:51Z
Last Changed At2026-05-29 23:01:55Z
Inactive At
Source Posted At2026-03-12 15:28:46Z
Source Updated At2026-05-19 20:19:17Z
Raw Payload Uris3://job-postings-prod-raw-590183727216/raw/provider=greenhouse/board=praxisprecisionmedicines/date=2026-06-06/2026-06-06T07-34-51-378Z-47bbfe4b8db4b6feb2b5d43e8b51117aff0cb8042317e416d94e5d4feb1723af.json
Event Fields
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  "last_changed_at": "2026-05-29T23:01:55.963Z",
  "active_status": "active"
}
Parsed Structured
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    "is_remote": true,
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  "inferred_at": "2026-06-06T07:34:51.525Z",
  "launch_scope": {
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  "salary_period": null,
  "workplace_type": "remote",
  "salary_currency": null
}
Extensions
{}
Native Structured
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  "metadata": [],
  "updated_at": "2026-05-19T16:19:17-04:00",
  "departments": [
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  ],
  "company_name": "Praxis Precision Medicines, Inc. ",
  "requisition_id": 4440863008,
  "first_published": "2026-03-12T11:28:46-04:00",
  "application_deadline": null
}
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