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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.

The Medical Director has primary responsibility for ensuring that the PV activities performed by assigned PV physicians are managed in a cost-efficient manner, are of the highest quality and in compliance with global regulations.

The Medical Director will:

• Lead, educate,mentor and develop the team of PV physicians to ensure their competence and confidence in developing their skills to become subject matter experts in pharmacovigilance.
• Actively monitor costs and project deliverables and interacting with the pharmacovigilance operational team.
• Ensure that all contracted PV physician activities are managed in compliance with regulations and company policies/procedures and in accordance with any PV agreements.
• Maintain good client relations and ensuring a consistently high quality of work for each client, creating trust in our expertise and services.

• Medically qualified as a physician
• Extensive experience in pharmacovigilance and clinical reasearch
• Eperience with leading or supporting the proactive monitoring and evaluation of all aspects of the safety profile of designated products
• Experience in reviewing of different aggregate report types including PADERs, PBRERs, DSURs, Annual Safety reports and RMPs
• Experience as a Qualified person for pharmacovigilance is essential
• Prior experience in supporting business development
• Leadership and managerial experience

Additional information

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

Come and join us in this exciting journey to make a positive impact in patient’s lives. We look forward to welcoming your application!