Remote Jobs RockRemote Jobs Rock

Pharmacovigilance Officer (senior level position)

📅 Jul 14
PharmacovigilanceIndividual Case Safety Report ProcessingSAE/SUSAR ManagementClinical Trial Reconciliation
Apply Now

📜 Description

  • Process Individual Case Safety Reports from clinical trials and post-marketing sources, including device and combination products.
  • Manage case workflows in line with applicable regulations, company procedures, client requirements, and timelines.
  • Independently manage SAE/SUSAR submissions, unblinding, and clinical trial reconciliations.
  • Prepare database outputs for periodic reports such as PBRER, DSUR, and PADER.
  • Mentor and train colleagues, and contribute to procedure optimization and development.

🛠️ Requirements

  • Life science / bio medical background – healthcare related degree (chemistry, biology, biotechnology, veterinary science) and demonstrated experience in Pharmacovigilance case processing
  • Demonstrated case processing experience
  • Time and issue management, delegation, organization and multitasking skills with good attention to detail
  • Strong interpersonal and communication skills
  • Advanced English skills, both verbal and written, at least C1
Full 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

At PrimeVigilance, PV Officers are independent case processing team members who are expected to manage a variety of case processing services with full accountability.  

If you join PrimeVigilance, you can expect to work with teams of different sizes, from small clinical trial, to large, generic post-marketing teams. We are always looking for proactive, capable and motivated individuals who aim to surpass any target set in front of them. 

The PV Officer should be a Life science / bio medical background graduate or have other healthcare related degree qualification (chemistry, biology, biotechnology, veterinary science etc.) and have demonstrated experience with several years in case processing. The PV Officer will be working as part of a project team, performing, and supporting contracted pharmacovigilance activities on behalf of PrimeVigilance.  

Responsibilities include:  

  • Processing of Individual Case Safety Reports from all sources (post-marketing and clinical trials, including device and combination products) in compliance with applicable regulations, PrimeVigilance procedures and in accordance with client specific requirements and timelines. As a key member there is an expectation to effectively cover all steps of a workflow cycle, except Medical Review. 
  • Independent SAE/SUSAR Management (submissions, unblinding, clinical trial reconciliations)  
  • Preparation of database outputs for periodic reporting (PBRER, DSUR, PADER, etc.) 
  • Mentoring and training of new and more junior employees within the department, including procedure optimization and development

Qualifications

  • Life science / bio medical background – healthcare related degree (chemistry, biology, biotechnology, veterinary science) and demonstrated experience in Pharmacovigilance case processing    
  • Demonstrated case processing experience 
  • Time and issue management, delegation, organization and multitasking skills with good attention to detail   
  • Strong interpersonal and communication skills   
  • Advanced English skills, both verbal and written, at least C1

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. 

Ergomed

Senior Pharmacovigilance Associate

🕒 14 days ago
Ergomed👥 501 - 1000 employees🏢 Biotechnology

Manage Individual Case Safety Reports (ICSRs) and related pharmacovigilance activities, ensuring regulatory and client requirements are met while supporting patient safety and timely safety-data reporting.

PharmacovigilanceICSR ManagementICSR Follow-upSAE/SUSAR Management
Summit Therapeutics

Associate Director, Patient Engagement and Advocacy

🕒 2 days ago
Summit Therapeutics👥 201 - 500 employees🏢 Biotechnology

Develop and improve patient engagement and advocacy strategies for ivonescimab, bringing patient perspectives into clinical development, Medical Affairs, education, and commercialization through compliant cross-functional programs.

Patient AdvocacyPatient EngagementOncologyMedical Affairs
Waymark

HEDIS Quality Programs, Principal

🕒 4 days ago
Waymark👥 51 - 200 employees🏢 Hospital & Health Care

Own and scale HEDIS and partner quality programs, translating measure requirements into operational workflows and campaigns while coordinating teams, vendors, analytics, and product partners to improve performance.

NCQA HEDISHealthcare Quality ProgramsQuality OperationsPopulation Health
Diverge Health

Care Management Clinical Lead

🕒 5 days ago
Diverge Health👥 51 - 200 employees🏢 Hospital & Health Care

Lead hands-on fee-for-service care management expertise, guiding health centers through clinical and billing questions, onboarding, workflow troubleshooting, and training that scales across the delivery team.

Fee-for-service Care ManagementChronic Care ManagementTransitions Of CareAdvanced Primary Care

Trusted by Remote Workers