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Pv Scientist Jobs (NOW HIRING)

Praxis Precision Medicines, Inc.

Senior PV Scientist

OR · On-site +1

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 ...

Biogen

Associate Director, PV Scientist

Cambridge, MA · On-site

$172K - $237K/yr

Serve as the lead PV Scientist for a specific product or group of products (investigational and/or marketed), providing strategic direction and scientific oversight. * Oversee signal detection and ...

Biogen

Associate Director, PV Scientist

Cambridge, MA · Hybrid

$172K - $237K/yr

Serve as the lead PV Scientist for a specific product or group of products (investigational and/or marketed), providing strategic direction and scientific oversight. * Oversee signal detection and ...

Praxis Precision Medicines, Inc.

Senior PV Scientist

$136K - $156K/yr

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 ...

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How much do pv scientist jobs pay per hour?

As of Jul 22, 2026, the average hourly pay for pv scientist in the United States is $61.42, according to ZipRecruiter salary data. Most workers in this role earn between $42.55 and $73.80 per hour, depending on experience, location, and employer.

What does a typical day look like for a PV Scientist?

A typical day for a PV Scientist involves reviewing and analyzing individual case safety reports, assessing potential safety signals, and preparing regulatory safety documents and risk management plans. You may participate in team meetings with cross-functional partners such as clinical, regulatory, and medical affairs teams to discuss ongoing safety concerns or emerging issues. Additionally, you’ll interact with global health authorities, respond to their inquiries, and ensure compliance with evolving drug safety regulations. The work is detail-oriented and deadline-driven, but it also offers valuable opportunities for professional growth and meaningful contributions to patient safety.

What are the key skills and qualifications needed to thrive in the Pv Scientist position, and why are they important?

To thrive as a PV (Pharmacovigilance) Scientist, you need an academic background in life sciences or pharmacy, in-depth knowledge of drug safety regulations, and strong analytical skills. Familiarity with pharmacovigilance databases (like Oracle Argus or ARISg), signal detection tools, and regulatory reporting systems is crucial, and certifications such as DSci or PV certifications are advantageous. Excellent written communication, critical thinking, and collaboration skills help you effectively interpret safety data and work cross-functionally. These competencies are essential for ensuring patient safety, regulatory compliance, and effective risk management in pharmaceutical environments.

What is a PV Scientist job?

A PV (Pharmacovigilance) Scientist is responsible for monitoring, assessing, and preventing adverse drug reactions to ensure patient safety. They analyze safety data, contribute to risk management plans, and prepare regulatory reports. PV Scientists collaborate with medical, regulatory, and clinical teams to ensure compliance with global safety regulations. Their role is critical in ensuring drug safety throughout a product’s lifecycle.

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Pv Scientist jobs near you
Infographic showing various Pv Scientist job openings in the United States as of July 2026, with employment types broken down into 94% Full Time, 3% Part Time, and 3% Contract. Highlights an 85% Physical, 5% Hybrid, and 10% Remote job distribution, with an average salary of $127,745 per year, or $61.4 per hour.
Senior PV Scientist

Senior PV Scientist

Praxis Precision Medicines, Inc.

OR • On-site, Remote

Other

Re-posted 11 days ago

Job 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. 

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