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Specialist, Regulatory and PV Network

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 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 is responsible for providing the strategy based on regulatory requirements and for completing regulatory and PV deliverables based on an established PV and regulatory plan. They also serve as a liaison between regulatory and other functional areas including external partners, clients, authorities and/or consultants in the planning, organizing, and preparing of regulatory deliverables following project, corporate and industry regulatory strategies. 

The Specialist will also act as Local Contact Person for the designated country.

Job Responsibilities

​​Role and Responsibilities​ 

  • Under the direction of a senior member of the team, assume leadership and functional representation for projects of low complexity assigned ensuring effective and rapid coordination and management of deliverables striving the team to meet the agreed targets and to comply with the agreed procedures, trackers and templates. 

  • Provide intelligence on requirements and contribute to the development of the strategy and set up activities (Project Management Plan, joint operating procedures, POAs and core documents). Support identification of issues and corrective actions. 

  • Collect, review, track and maintain LCPs' CVs, job descriptions, training records, contact details and monthly reports. 

  • Ensure correct training assignment to and training compliance by the LCPs. 

  • Promptly identify and escalate risk/potential risk to the project team which may jeopardise deliverables. 

  • Provide Clients expertise and guidance at national level. 

  • Maintain awareness of allocated tasks and hours and promptly identify and escalate any OoS. 

  • Prepare client’s invoices and review/ approve vendors’ project invoices. 

  • Provide support to proposal development and input to budgets, provide department representation to BD meetings as required. 

  • 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. 

  • Participate in preparation for audits/inspections and provide department representation for assigned projects as required. 

  • Track LCPs' key performance indicators and prepare monthly summary reports. 

  • Provide feedback on performance of vendors to aid their assessment. 

  • Communicate suggestions for changes to departmental/company processes/procedures.   

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, both written and verbal
  • Candidate must be proficient in the official language of the country in which they are based, as this is essential for local interactions and compliance.
  • 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  

We look forward to welcoming your application. 

#LI remote

What You Should Know About Specialist, Regulatory and PV Network, Ergomed

At PrimeVigilance, part of Ergomed Group, we are on a mission to ensure the safety and efficacy of pharmaceutical products across the globe, and we are excited to welcome a Specialist in Regulatory and PV Network to our vibrant team in Lisbon, Portugal. As a crucial member of our organization, you will take the lead on regulatory strategies and pharmacovigilance objectives, collaborating with clients and partners to provide top-notch deliverables. Your role will involve overseeing project management plans, ensuring compliance with regulatory requirements while fostering impactful relationships within our dynamic network. You’ll be empowered to conduct risk assessments, track performance metrics, and provide insights that drive quality outcomes. With a focus on continuous learning and professional development, we aim to provide an inspiring work environment where everyone’s contribution is valued. If you have a background in Life Sciences or Nursing and are passionate about improving patient safety, this is the perfect opportunity to grow your career with a leading pharmacovigilance service provider. Join us and make a difference in lives around the world while enjoying a supportive, multifaceted work culture at PrimeVigilance!

Frequently Asked Questions (FAQs) for Specialist, Regulatory and PV Network Role at Ergomed
What are the main responsibilities of a Specialist, Regulatory and PV Network at PrimeVigilance?

The Specialist, Regulatory and PV Network at PrimeVigilance is responsible for leading the regulatory strategy, ensuring that pharmacovigilance and regulatory deliverables are aligned with project goals. This position entails liaising with various stakeholders, managing project timelines and deliverables, and maintaining regulatory intelligence to stay updated with changing legislation.

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What qualifications are required for the Specialist, Regulatory and PV Network position at PrimeVigilance?

To qualify for the Specialist, Regulatory and PV Network role at PrimeVigilance, candidates should hold a Bachelor's Degree in Chemistry or Life Sciences, Nursing, or have equivalent experience. Additionally, previous experience within the pharmaceutical or CRO industry, along with fluency in English and the official language of the host country, are essential.

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How does PrimeVigilance support its employees working in the Specialist, Regulatory and PV Network role?

PrimeVigilance is committed to the professional growth of its employees, including those in the Specialist, Regulatory and PV Network role. The company offers training programs, opportunities for career development, and emphasizes a work-life balance to ensure employee well-being and a satisfying professional journey.

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What is the work environment like for a Specialist, Regulatory and PV Network at PrimeVigilance?

The work environment at PrimeVigilance is friendly and collaborative, centered around teamwork and mutual support. As a Specialist, you will engage with colleagues from around the world, fostering professional relationships while benefiting from a culture that prioritizes diversity, equity, and inclusion.

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What skills are essential for succeeding as a Specialist, Regulatory and PV Network at PrimeVigilance?

Success in the Specialist, Regulatory and PV Network role at PrimeVigilance requires strong planning and organizational skills, attention to detail, and effective communication abilities. Candidates should also possess strong interpersonal skills and the capability to thrive in a fast-paced, deadline-oriented environment.

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Common Interview Questions for Specialist, Regulatory and PV Network
Can you describe your experience in managing regulatory projects?

When answering this question, highlight specific regulatory projects you have worked on, detailing your role, the challenges faced, and the strategies you implemented to ensure compliance and deliver successful outcomes.

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How do you stay updated with changing regulations in pharmacovigilance?

Discuss your methods for keeping abreast of new regulatory developments, such as attending industry conferences, subscribing to relevant journals, or participating in professional networks, and explain how this knowledge enhances your work.

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What is your approach to risk management in a regulatory project?

Explain your systematic approach to identifying, assessing, and mitigating risks within a project. Provide examples of how you've successfully navigated past risks and the tools or methodologies you used.

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How do you foster strong relationships with clients and stakeholders?

Share specific strategies you employ to build trustworthy relationships, such as regular communication, transparency in processes, or involving clients in decision-making. Emphasize the importance of understanding client needs.

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Can you give an example of how you handled a compliance issue in the past?

Provide a detailed account of a compliance challenge you faced. Focus on your analysis of the situation, the corrective actions you implemented, and the lessons learned to ensure it won’t happen again.

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Explain how you prioritize multiple deliverables and deadlines.

Demonstrate your organizational skills by discussing your prioritization process, including the use of project management tools, tracking systems, or time management techniques to meet tight deadlines without compromising quality.

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What relevant software tools are you proficient in for regulatory reporting?

List specific software tools you have used for regulatory reporting, detailing your level of expertise and how these tools have improved your efficiency and accuracy in reporting.

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What strategies do you use to ensure effective training and compliance for Local Contact Persons (LCPs)?

Discuss your approach to training LCPs, emphasizing the importance of clear communication of expectations, ongoing support, and mechanisms for tracking compliance. Mention any tools you’ve used to facilitate this process.

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How do you handle feedback about performance from vendors?

Explain your constructive approach to providing feedback, focusing on fostering positive relationships while delivering honest evaluations that encourage improvement and collaboration.

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What do you consider when preparing for audits or inspections?

Discuss your preparation strategies for audits or inspections, including the documentation processes, team readiness, and the importance of thorough review to ensure compliance with all regulatory requirements.

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Founded in 1997, Erogmed is a global provider of clinical trial planning, management, and monitoring; and drug safety and medical information services. The company offers clinical development, trial management, and pharmacovigilance services for p...

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Full-time, remote
DATE POSTED
December 15, 2024

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