Qualified Person Responsible for Pharmacovigilance QPPV in the EU and UK homebased

Ergomed; Madrid; Presencial; EUR 40.000 - 80.000; Jornada completa

Descripción de la vacante

Join a forward-thinking company dedicated to improving patient lives through pharmacovigilance. This role as EU QPPV involves ensuring compliance with safety regulations and managing adverse reaction reports. You'll leverage your expertise in global regulations and lead initiatives that prioritize patient safety. With a commitment to diversity and employee well-being, this organization fosters a supportive environment for professional growth and collaboration. If you're passionate about making a difference in the pharmaceutical industry, this opportunity is perfect for you.

Servicios

Training and career development opportunities

Friendly, supportive working environment

Opportunity to work with international colleagues

Formación

• Strong knowledge of global regulations and best practices in pharmacovigilance.
• Experience as a QPPV with operational and managerial skills.

Responsabilidades

• Establish and maintain systems for reporting adverse reactions.
• Provide information to regulatory authorities regarding safety evaluations.

Conocimientos

Pharmacovigilance

Regulatory Affairs

Safety Surveillance

Project Management

Communication Skills

Educación

Life-science education (Medicine or Pharmacy)

Descripción del empleo

Company Description

We are PrimeVigilance (part of Ergomed PLC), a specialised mid-size pharmacovigilance service provider initially 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 becoming one of the global leaders in its fields. We cover all therapy areas including medical devices.

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.

Job Description

The EU QPPV is responsible for:

• The establishment and maintenance of a system which ensures that information about all suspected adverse reactions which are reported to the personnel of the Company, and to medical representatives, is collected and collated in order to be accessible at least at one point within the Community;
• Ensuring that any request from the CAs for the provision of additional information necessary for the evaluation of the benefits and risks afforded by a medicinal product is answered fully and promptly;
• Provision to the CAs, of any other information relevant to the evaluation of the benefits and risks afforded by a medicinal product, including appropriate information on planned post-authorisation safety studies.
• Being continuously available to CAs in Member States and the Agency and the MAH, ensuring adequate back-up procedures are in place.
• Having an oversight of the safety aspects of the company’s medicinal products including an overview of medicinal product safety profiles, any emerging safety concerns, any conditions or obligations adopted as part of the marketing authorisations and other commitments relating to safety or the safe use of the products and other relevant finding raised from studies/programmes conducted by the Company.

Qualifications

• Life-science education background Medicine (human or veterinary) or Pharmacy preferred
• Solid knowledge of PV system operations and function
• Strong knowledge of Global Regulations, standards and best practices regarding safety processing and reporting, safety surveillance and pharmaceutical industry compliance activities in post-marketing
• Strong operational and managerial skills as demonstrated by leading previous projects or functions
• Strong experience in a PV role, profound experience as QPPV
• Strong oral and written English communication skills

Additional Information

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.