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Primevigilance Jobs in Raleigh, NC (NOW HIRING)

Ergomed

Senior Submissions Officer

Raleigh, NC · On-site

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 ...

Ergomed

Senior Submissions Officer

Raleigh, NC · On-site +1

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 ...

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$25

$59

How much do primevigilance jobs pay per hour?

As of Aug 13, 2026, the average hourly pay for primevigilance in Raleigh, NC is $25.46, according to ZipRecruiter salary data. Most workers in this role earn between $14.64 and $29.74 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive in the primevigilance position?

To thrive in a Pharmacovigilance Specialist role at PrimeVigilance, you need a solid background in life sciences or pharmacy, knowledge of drug safety regulations, and experience with pharmacovigilance processes. Proficiency with safety databases (such as Argus or ARISg), standard coding systems (MedDRA, WHO-DRUG), and relevant certifications like a PV certification or GVP training are highly valuable. Excellent attention to detail, strong analytical thinking, written communication skills, and the ability to work collaboratively stand out in this position. These skills ensure the accuracy and integrity of safety data, compliance with regulatory standards, and effective teamwork in monitoring the safety of medicinal products.

What are some typical daily responsibilities of a pharmacovigilance specialist at Primevigilance?

Pharmacovigilance Specialists at PrimeVigilance are responsible for processing and evaluating adverse event reports, performing case assessments, writing and submitting regulatory reports, and maintaining accurate drug safety documentation. The role involves communicating with healthcare professionals, clients, and regulatory authorities to clarify or follow up on safety information. On a daily basis, you will use safety databases and coding systems to ensure data accuracy and consistency while contributing to ongoing risk management activities. This position typically works as part of a multidisciplinary team and offers opportunities to collaborate with medical writers, regulatory experts, and clinical research professionals.

What is a primevigilance?

A Primevigilance job typically involves roles in pharmacovigilance, which focuses on drug safety and monitoring adverse effects of pharmaceutical products. Professionals in this field assess and report adverse drug reactions (ADRs), ensure regulatory compliance, and contribute to risk management. Roles may include drug safety associates, medical reviewers, and regulatory specialists. These jobs are crucial for maintaining patient safety and supporting healthcare professionals with accurate drug safety data.

What job categories do people searching Primevigilance jobs in Raleigh, NC look for? The top searched job categories for Primevigilance jobs in Raleigh, NC are:
What cities near Raleigh, NC are hiring for Primevigilance jobs? Cities near Raleigh, NC with the most Primevigilance job openings:
Primevigilance jobs near you
Infographic showing various Primevigilance job openings in Raleigh, NC as of August 2026, with employment types broken down into 100% Full Time. Highlights an 67% Physical, and 33% Remote job distribution, with an average salary of $52,960 per year, or $25.5 per hour.

Senior Submissions Officer

PrimeVigilance

Raleigh, NC

Full-time

Posted 6 days ago

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
  • Supporting the client in all aspects of safety submission
  • Supports the Submission Manager in development, documentation, implementation and maintenance of submission processes and standards
  • Ensures personal knowledge and understanding of global regulatory reporting requirements to ensure compliance
  • Performing submissions of ICSRs/aggregate reports to all concerned parties
  • Performing exchanges of ICSRs with all concerned parties as per applicable documents
  • Providing support in all PV operations associated with Safety Reporting
  • Performing Quality control of ICSR Reportability Assessment
  • Performing Quality control of daily safety submission activities
  • Active participation in trainings, maintenance and development of quality system documents for Safety Reporting area
  • Provide training for junior members of the team
  • Acts as an SME for Submissions in audits and inspections representing Submissions business processes and standards
Qualifications
  • Life science graduate, pharmacy, nursing or other healthcare related qualification
  • 3-5 years of work experience in pharmacovigilance with at least 2 years of experience working on submissions
  • Organization skills, including attention to detail and multitasking
  • Management skills, including time and issue management
  • Communication skills, including clear and effective interaction with internal and external stakeholders

English - fluent (spoken, written)


Additional Information

Why PrimeVigilance?

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.