Junior PV Officer
Raleigh, NC · On-site
PrimeVigilance provides first class support to our small to large pharmaceutical and biotechnology partners maintaining long lasting relationships and has become one of the global leaders in its ...
Raleigh, NC · On-site
PrimeVigilance provides first class support to our small to large pharmaceutical and biotechnology partners maintaining long lasting relationships and has become one of the global leaders in its ...
Raleigh, NC · On-site
PrimeVigilance provides first class support to our small to large pharmaceutical and biotechnology partners maintaining long lasting relationships and has become one of the global leaders in its ...
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 ...
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 ...
$8.60 - $13.24
16% of jobs
$14.66 is the 25th percentile. Wages below this are outliers.
$13.24 - $17.89
29% of jobs
The median wage is $19.05 / hr.
$17.89 - $22.54
19% of jobs
$26.66 is the 75th percentile. Wages above this are outliers.
$22.54 - $27.19
12% of jobs
$27.19 - $31.83
8% of jobs
$31.83 - $36.48
5% of jobs
$36.48 - $41.13
4% of jobs
$41.13 - $45.77
2% of jobs
$45.77 - $50.42
2% of jobs
$50.42 - $55.07
1% of jobs
$55.07 - $59.71
1% of jobs
$8
$25
$59
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.
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.
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.

We are PrimeVigilance (part of Ergomed PLC), a specialised mid-size pharmacovigilance service provider established in 2008. We are proud to have achieved global organic growth year after year, with staff based across Europe, North America and Asia all covering services within: Medical Information, Pharmacovigilance, Regulatory Affairs and Quality Assurance.
PrimeVigilance provides first class support to our small to large pharmaceutical and biotechnology partners maintaining long lasting relationships and has become one of the global leaders in its field. We cover all therapy areas including medical device.
We love investing in our staff by providing an excellent training and development platform. We value employee experience, well-being and mental health and we acknowledge that a healthy work life balance is a critical factor for employee satisfaction and in turn nurtures an environment from which a high-quality client service can be achieved.
Come and join us in this exciting journey to make a positive impact in patient's lives.
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
Requirements:
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)
Why PrimeVigilance?
We prioritize diversity, equity, and inclusion by creating an equal opportunities workplace and a human-centric environment where people of all cultural backgrounds, genders and ages can contribute and grow.
To succeed we must work together with a human first approach. Why? because our people are our greatest strength leading to our continued success on improving the lives of those around us.
We offer:
Our core values are key to how we operate, and if you feel they resonate with you then PrimeVigilance could be a great company to join!
We look forward to welcoming your application.
Sourced by ZipRecruiter
Medical equipment and supplies manufacturing
1 - 10 Employees
San Antonio, TX, US
1987