Pharmacovigilance Regulatory Affairs Specialist

vor 1 Woche


Frankfurt am Main, Deutschland PrimeVigilance Vollzeit

Company Description

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.

**Job Description**:
The Specialist, Regulatory and PV network will assume leadership and functional representation for projects assigned and coordinate the local contact persons responsible for regulatory and pharmacovigilance activities.

The Specialist will also act as local contact person for the designated country.

**Responsibilities**:

- Ensure the effective and rapid coordination and management of project deliverables to meet the agreed targets and to comply with the agreed procedures, trackers and templates.
- Provide Clients expertise and guidance at national level.
- Set-up and coordinate the network of local contact persons(LCPs) for RA and PV in assigned projects
- Foster professional working relationships with internal and external contacts at the local and international levels to ensure smooth and efficient service delivery.
- Stay abreast of changing regulatory legislative requirements and ensure maintenance of the regulatory intelligence database and timely dissemination of pertinent changes.
- Manage LCPs training and assess key performance indicators
- Act as main point of contact with the clients for Regulatory and PV network activities
- Managing project budget including vendor costs
- Act as primary contact person for local regulatory authority / Pharmacovigilance expert in assigned countries
- Participate in preparation for audits/inspections and provide department representation for assigned projects as required.
- Provide feedback on performance of vendors to aid their assessment.
- Review and linguistic input on local Product Information and Mock-ups
- Perform local non-indexed literature screening and screening of Regulatory Authority website/s (if applicable for the Client) for potential Adverse Drug Reactions (ADRs) and safety information

**Qualifications**:

- Bachelor's Degree in Chemistry or Life Sciences, Nursing, or equivalent experience
- Previous experience within the pharmaceutical/CRO industry
- PV training and/or working experience and other educational or professional background as required locally
- Fluent in English and German, both written and verbal
- Good planning and organizational skills
- Strong interpersonal skills in a fast-paced, deadline oriented, and changing environment
- Good attention to detail

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

LI remote



  • Frankfurt am Main, Hessen, Deutschland PrimeVigilance Vollzeit

    Company DescriptionPrimeVigilance (part of Ergomed Group), is 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...


  • Frankfurt am Main, Hessen, Deutschland PrimeVigilance Vollzeit

    Company Description PrimeVigilance (part of Ergomed Group), is 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...


  • Frankfurt am Main, Deutschland Medella Life Vollzeit

    Job Title: Senior Regulatory Manager (Pharmaceuticals – Dermatology) Job Summary The Senior Regulatory Manager is responsible for leading regulatory affairs activities for pharmaceutical products, with a particular focus on dermatology. This role ensures regulatory compliance across the full product lifecycle and provides strategic regulatory guidance to...


  • Frankfurt am Main, Deutschland STERIS Vollzeit

    **Über HuFriedyGroup**: Die HuFriedyGroup ist mit insgesamt über 177 Jahren Erfahrung in der Dentalindustrie weltweit führend in den Bereichen Infektionsprävention, Instrumentenherstellung und Wiederaufbereitung von Instrumenten. Die HuFriedyGroup hilft Zahnärzten dabei, ‚Best in Practice‘ zu sein, indem sie einen geschlossenen ‚Circle of...


  • Frankfurt, Deutschland Medella Life Vollzeit

    Job Title: Senior Regulatory Manager (Pharmaceuticals – Dermatology)Job SummaryThe Senior Regulatory Manager is responsible for leading regulatory affairs activities for pharmaceutical products, with a particular focus on dermatology. This role ensures regulatory compliance across the full product lifecycle and provides strategic regulatory guidance to...


  • Ingelheim am Rhein, Deutschland engineering people GmbH Vollzeit

    Aufgaben: - preparation and finalization of safety update reports for submission - mapping stock keeping units linked to sales data and calculation of sold doses - performing data quality checks and reviewing regulatory information to identify pharmacovigilance related safety actions or request regulatory information from regulatory affairs managers -...


  • Frankfurt am Main, Deutschland Syneos Health Clinical Vollzeit

    **Overview** **Base location: Neu-Isenburg** **Regions covered: Germany** The Global Safety Regions Specialist (GSRS) will follow the strategic direction for Global Safety Regions while establishing and maintaining it globally. The GSRS will also maintain the locally needed standardised practices to ensure compliance with international and national...


  • Frankfurt am Main, Deutschland Axiom Talent Platform Vollzeit

    We are currently seeking a Pharmaceutical Regulatory and Compliance Legal Counsel (M/F/d) to work with a our client, a F100 technology company] in-house. This is an exciting opportunity where you can bring your legal background and business acumen to work on cutting-edge while tackling complex legal challenges on a global scale. This opportunity enables you...


  • Frankfurt am Main, Hessen, Deutschland IFRS Foundation Vollzeit

    Location: Frankfurt or London. The IFRS Foundation operates under a multi-location operating model; morning and evening calls will occur occasionally. Duration: month contract Reports to:      Director of Regulatory Implementation Job purpose:  The Regulatory Affairs Manager plays a key role in the design, development and delivery of an effective...


  • Frankfurt am Main, Deutschland Deutsche Börse Vollzeit

    **Learn. Develop. Grow. But always: Share value**: Join our international team that drives positive change, united by a spirit of openness and curiosity. We empower you to have an impact and to grow - personally and professionally. With us, you work at the heart of financial systems and evolve the way markets operate. We’re excited about the future because...