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- Tasks: Lead critical assessments of medical products, ensuring patient safety and effective communication.
- Company: Join the MHRA, a leading regulator transforming healthcare for better patient outcomes.
- Benefits: Enjoy a dynamic work environment with opportunities for professional growth and collaboration.
- Why this job: Make a real impact on public health while working with innovative teams and diverse stakeholders.
- Qualifications: Must have regulatory experience and expertise in Vaccines, Infectious Diseases, or Diagnostics.
- Other info: Opportunity to mentor junior staff and engage directly with patients and the public.
The predicted salary is between 48000 - 72000 £ per year.
The MHRA is transforming. Through enabling innovation, making the right judgements of the benefits and risks of medical products, and forging the right partnerships in the UK and internationally, it aims to deliver world-class regulation and improved outcomes for UK patients.
We are currently looking for an experienced Senior Benefit Risk Evaluation Assessors to join our Benefit/Risk Evaluation Team II in the Safety and Surveillance group.
Within a week of working here, your day could look like this: deliver on our ongoing work and increase capacity to respond to new-emerging safety issues.
The successful candidate will have comprehensive medicines regulatory experience as well as professional, technical, or scientific expertise in the Vaccines, Infectious Diseases, and Diagnostics therapeutic area. The experience of the successful applicant will be vital in helping to support new members of the team build their competencies.
- Lead, influence, or deliver consistently high-quality critical appraisals/assessment projects for significant safety or risk-benefit issues, evaluating all relevant information sources including real-world evidence in accordance with agreed timelines, seeking expert advice where needed, and ensuring the patient experience is duly considered.
- Actively engage with patients and the public, key external stakeholders, government departments, professional bodies, and the wider health sector.
- Develop communications for the public, senior officials, or ministers as required, and provide scientific, technical, and clinical input to ensure regular and timely advice is communicated to healthcare professionals.
- Lead and develop cross-portfolio projects, identifying and deploying resources and mentoring more junior staff as required to achieve agency patient safety goals.
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Senior Benefit Risk Evaluation Assessors x2 employer: Mhra
Contact Detail:
Mhra Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Senior Benefit Risk Evaluation Assessors x2
✨Tip Number 1
Familiarise yourself with the latest developments in benefit-risk evaluation, particularly in the context of vaccines and infectious diseases. This will not only enhance your understanding but also demonstrate your commitment to staying updated in this rapidly evolving field.
✨Tip Number 2
Network with professionals in the regulatory and safety sectors. Attend relevant conferences or webinars where you can meet current employees from the MHRA or similar organisations. Building these connections can provide valuable insights and potentially lead to referrals.
✨Tip Number 3
Prepare to discuss real-world evidence and its application in benefit-risk assessments during interviews. Being able to articulate how you have used such data in past roles will set you apart as a candidate who understands the practical implications of your work.
✨Tip Number 4
Showcase your mentoring experience when engaging with the team. Highlight any instances where you've supported junior staff or led projects, as this aligns with the role's requirement for leadership and development within the team.
We think you need these skills to ace Senior Benefit Risk Evaluation Assessors x2
Some tips for your application 🫡
Understand the Role: Before applying, make sure to thoroughly understand the responsibilities and requirements of the Senior Benefit Risk Evaluation Assessor position. Familiarise yourself with the MHRA's mission and how this role contributes to patient safety.
Tailor Your CV: Highlight your relevant experience in medicines regulation, particularly in Vaccines, Infectious Diseases, and Diagnostics. Use specific examples that demonstrate your ability to lead assessments and engage with stakeholders effectively.
Craft a Compelling Cover Letter: Write a cover letter that showcases your passion for patient safety and your expertise in benefit-risk evaluation. Mention any experience you have in mentoring junior staff and leading cross-portfolio projects, as these are key aspects of the role.
Proofread and Edit: Before submitting your application, carefully proofread your documents for any spelling or grammatical errors. Ensure that your writing is clear and professional, reflecting the high standards expected by the MHRA.
How to prepare for a job interview at Mhra
✨Showcase Your Regulatory Experience
Make sure to highlight your comprehensive medicines regulatory experience during the interview. Be prepared to discuss specific examples of how you've evaluated benefits and risks in medical products, particularly in the areas of Vaccines, Infectious Diseases, and Diagnostics.
✨Demonstrate Leadership Skills
Since the role involves mentoring junior staff and leading projects, be ready to share instances where you've successfully led a team or project. Discuss how you influenced outcomes and supported team members in building their competencies.
✨Engage with Stakeholders
The position requires active engagement with various stakeholders. Prepare to talk about your experience in collaborating with patients, public bodies, and government departments. Highlight any successful communication strategies you've employed to convey complex information.
✨Prepare for Real-World Evidence Discussions
As evaluating real-world evidence is crucial for this role, brush up on recent developments in this area. Be ready to discuss how you've incorporated real-world data into your assessments and how it has impacted patient safety outcomes.
