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. 

• Support the client in all aspects of safety reporting for aggregate reports and related activities
• Performing submissions of aggregate reports to all concerned parties
• Performing and oversight of reporting’s   of Aggregate reports to Regulatory Authorities (RAs), Ethics Committees (ECs), Institutional Review Boards (IRB) and Investigators
• Tracking and archiving Aggregate reports submissions and exchanges 
• Supporting the client with EudraVigilance registration and maintenance of EudraVigilance account for client
• Support in all PV operations associated with safety reporting for aggregate reports and related activities
• Quality control of daily safety reporting activities
• Active participation in trainings, maintenance and development of quality system documents for Safety Reporting area
• Participating in Audits and Inspections

• Life science / bio medical background – healthcare related degree (chemistry, biology, biotechnology, veterinary science) and demonstrated experience in Pharmacovigilance safety submissions   
• Demonstrated aggregate report submission experience to RAs/ECs
• eCTD sequencing experience is preffered
• 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  

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: 

• Training and career development opportunities internally  
• Strong emphasis on personal and professional growth 
• Friendly, supportive working environment 
• Opportunity to work with colleagues based all over the world, with English as the company language 

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!  

• Quality 
• Integrity & Trust  
• Drive & Passion  
• Agility & Responsiveness  
• Belonging 
• Collaborative Partnerships  

We look forward to welcoming your application.