Ergomed
Senior Submissions Officer
At a Glance
- Location
- Raleigh, North Carolina, United States
- Employment
- Full-time
- Experience
- 3–5 years
- Department
- ICSR Management
- Posted
- 2026-08-05T20:49:23.749Z
Key Requirements
Domain Knowledge
- Healthcare
Requirements
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)
Compensation & Benefits
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.
Responsibilities
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
About the Company
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.