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Junior PV Officer

Role overview

Qualifications

  • Life science / bio medical background – healthcare related degree (chemistry, biology, biotechnology, veterinary science)
  • Minimum 2 years of work experience in pharmacovigilance
  • Excellent communication (written and verbal) skills
  • English – fluent (spoken, written)

Responsibilities

  • Providing support to other activities undertaken by the project team on behalf of the client and the company
  • Processing Individual Case Safety Reports (ICSRs) from all sources in compliance with applicable regulations
  • Performing ICSR follow up and SAE/SUSAR Management
  • Mentoring and training of new and more junior employees within the department

Key facts

Other skills

  • Teamwork
  • Detail Oriented
  • Multitasking
  • Planning
  • Time Management
  • Microsoft Office
  • Communication

About the company

PrimeVigilance logo

PrimeVigilance

Contract Research Organizations (CRO)

PrimeVigilance, an Ergomed company, was set up by former Pharmacovigilance Regulators in 2008. We have grown to become the leading Pharmacovigilance specialist company, delivering global solutions for both clinical safety and post-marketing pharmacovigilance, as well as medical information from our offices. Having successfully delivered Pharmacovigilance (PV) and Medical Information (MI) services for over 14 years, our experience enables us to offer a comprehensive, top quality, cost-effective, and innovative safety solution. Our flexible approach, tailor-made to work with clients, allows us to deliver the services that meet your clinical and post-marketing needs.From its operational hubs based in Europe, the USA, and Japan. PrimeVigilance manages a global Pharmacovigilance system with a choice of leading drug safety databases, stretching to more than 100 countries.• 900+ highly qualified professionals• Global leader in QPPV services• 24/7 multilingual call center• Choice of leading drug safety databases• Robotic Process Automation (RPA) expertise• Access to regulatory experts and key opinion leadersGLOBAL LIFE CYCLE MANAGEMENT SERVICES• PHARMACOVIGILANCE • PHARMACOEPIDEMIOLOGY & BENEFIT-RISK MANAGEMENT• AUDIT & INSPECTION• QUALITY MANAGEMENT• REGULATORY SCIENCE

Company details

IndustryContract Research Organizations (CRO)
Company size501 - 1000

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Job description

Company Description

Medicine moves forward here. So will you. 

At PrimeVigilance, patient safety is not one part of the job. It is why we exist. 

We are a global pharmacovigilance specialist. Our teams help clients navigate complex regulations while keeping patient safety at the center of every decision, from early development through to post-marketing surveillance. Increasingly, the value we create is not only in processing safety data but in interpreting it: spotting the signal that matters early and turning it into insight our clients can act on. 

That work takes curious minds, problem-solvers and experts who care about getting it right. It also takes a culture worth staying for. Across Europe, North America, South America, Asia and Australia, we work in an environment built on kindness, flexibility, growth and belonging, where colleagues support one another and good ideas are heard wherever they come from. 

If you want a role with real purpose, global reach and the chance to keep growing while you help protect patients, you will feel at home here. We would love to hear from you. 

Job Description

  • Providing support to other activities undertaken by the project team on behalf of the client and the company 

  • Performing activities in the scope of ICSR management unit within agreed extent and timeframe (including, but not limited to): 

  • Processing Individual Case Safety Reports (ICSRs) from all sources in compliance with applicable regulations, PrimeVigilance procedures and in accordance with client specific requirements and timelines 

  • Performing ICSR follow up 

  • SAE/SUSAR Management (unblinding, clinical trial reconciliation, protocol review, Safety Management Plan review) 

  • Reconciliation (clinical, partners) 

  • Personal data protection 

  • Product Quality Complaint handling and interaction with Quality Assurance 

  • Medical Information interaction 

  • MedDRA and WHO coding 

  • Database Outputs and Reports (including data for monthly reporting to clients) 

  • Workflow & resource management 

  • Mentoring and training of new and more junior employees within the department 

  • Support of PV processes related to the ICSR management within PrimeVigilance and also to clients 

  • More senior colleague may perform tasks assigned as per SOP to more junior position 

  • Performing activities in the scope of ICSR management unit within agreed extent and timeframe 

  • Supporting the RA & PV Network Department as needed, including acting as the LCPPV (Local Contact Person for Pharmacovigilance) for the specified country and taking on the role of PRLS (Person Responsible for Local Screening) for the designated language, as agreed with the line manager 

 

 

 

Qualifications

Requirements:  

  • Life science / bio medical background – healthcare related degree (chemistry, biology, biotechnology, veterinary science) and demonstrated experience in Pharmacovigilance case processing    
  • Minimum 2 years of work experience in pharmacovigilance 
  • Excellent communication (written and verbal) skills 

  • Organization skills, including attention to details and multitasking 

  • Delegation skills 

  • Planning and time management 

  • Technical skills 

  • Team working 

  • English – fluent (spoken, written) 

  • Advanced literacy (MS Office) 

Additional Information

When you join Ergomed Group, you make a difference by helping to bring safe and effective pharmaceutical treatment to patients around the world. You’ll join a passionate and collaborative team of experts in clinical research, pharmacovigilance, and quality consulting.  

We are diverse in many ways, yet our values unite us. Our values are how we work, not words on a wall. If they sound like you, you will feel at home here. 

  • Quality: we hold ourselves to the standard patients deserve. 

  • Integrity and trust: we do the right thing, especially when it is hard. 

  • Drive and passion: we care about the outcome, because someone is waiting on it. 

  • Agility and responsiveness: we move quickly, because patients cannot wait. 

  • Belonging: everyone is welcome, and every voice counts. 

  • Collaborative partnerships: we go further by going together. 

We look forward to welcoming your application. 

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MR

Marcus Rivera

Chief Revenue Officer

m.rivera@company.com
linkedin.com/in/marcusrivera
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