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- Tasks: Conduct PV audits, ensure compliance, and support risk management activities.
- Company: Join ProPharma, a leader in improving health through innovative consulting solutions.
- Benefits: Flexible remote work with opportunities for professional growth and collaboration.
- Other info: Diverse and inclusive workplace that values your unique contributions.
- Why this job: Make a real impact in pharmacovigilance while working with top-tier clients.
- Qualifications: BSc in life sciences and extensive experience in pharmacovigilance required.
The predicted salary is between 36000 - 60000 £ per year.
For the past 20 years, ProPharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech, med device, and pharmaceutical organizations of all sizes to confidently advance scientific breakthroughs and introduce new therapies. As the world’s largest RCO (Research Consulting Organization), ProPharma partners with its clients through an advise-build-operate model across the complete product lifecycle.
We are currently supporting a leading Biological client as they require Pharmacovigilance support on an operational and strategic basis. This project will support activities in PV Quality Assurance; PV auditing and Risk management activities while also working with other projects as and when required. Currently we are looking to partner with an experienced PV professional (independent Consultant) who has the availability to start immediately for a 6 month period on a full time basis. The project can be performed largely remotely but with 1x trip to the Benelux region throughout the 6 month period.
Key responsibilities- Actively conduct PV audits across the group which includes all follow up activities
- Ensure full compliance with all necessary regulations globally
- Support any ongoing inspections when requested
- Support and lead deviations and CAPA activities
- Perform Risk assessments as and when required
- Support Risk management activities
- Provide overall guidance and support for our clients Pharmacovigilance activities
- Educated to a BSc level or higher within a life-sciences discipline
- Highly experienced within the Pharmacovigilance area
- Proven skills working on PV QA, PV auditing and supporting Risk management activities is preferred
- Thorough understanding of the Regulations within the Pharmacovigilance area
- Able to support projects both operationally and strategically
- Fluency in English is a must
- Must currently reside in the UK or EU
- Can perform the project to the required level as specified in the job description
We celebrate our differences and strive to create a workplace where each person can be their authentic self. We are committed to diversity, equity, and inclusion. Employees are encouraged to unleash their innovative, collaborative, and entrepreneurial spirits. With a holistic approach as an Equal Opportunity Employer, we provide a safe space where all employees feel empowered to succeed.
Freelance/Contract Pharmacovigilance Consultant - PV QA/Auditing in Wolverhampton employer: ProPharma
Contact Detail:
ProPharma Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Freelance/Contract Pharmacovigilance Consultant - PV QA/Auditing in Wolverhampton
✨Tip Number 1
Network like a pro! Reach out to your connections in the pharmacovigilance field and let them know you're on the lookout for opportunities. You never know who might have a lead or can put in a good word for you.
✨Tip Number 2
Get your online presence sorted! Make sure your LinkedIn profile is up-to-date and showcases your skills in PV QA and auditing. Join relevant groups and engage with posts to get noticed by potential employers.
✨Tip Number 3
Prepare for interviews by brushing up on your knowledge of regulations and risk management in pharmacovigilance. Be ready to discuss your past experiences and how they relate to the role you're applying for.
✨Tip Number 4
Don't forget to apply through our website! It’s the best way to ensure your application gets seen by the right people. Plus, it shows you're serious about joining the team at ProPharma.
We think you need these skills to ace Freelance/Contract Pharmacovigilance Consultant - PV QA/Auditing in Wolverhampton
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to highlight your experience in Pharmacovigilance, especially in QA and auditing. We want to see how your skills align with the key responsibilities mentioned in the job description.
Craft a Compelling Cover Letter: Your cover letter should tell us why you're the perfect fit for this role. Share specific examples of your past work in PV and how it relates to the project at hand. We love a good story!
Showcase Your Regulatory Knowledge: Since understanding regulations is crucial for this role, make sure to mention any relevant certifications or training you've completed. We need to know you can navigate the regulatory landscape with ease.
Apply Through Our Website: Don't forget to apply through our website! It’s the best way for us to receive your application and ensures you’re considered for the role. Plus, we love seeing applications come directly from interested candidates.
How to prepare for a job interview at ProPharma
✨Know Your Pharmacovigilance Stuff
Make sure you brush up on your knowledge of pharmacovigilance regulations and practices. Be ready to discuss your experience with PV QA, auditing, and risk management in detail. This will show that you’re not just familiar with the field but also have hands-on experience.
✨Prepare for Scenario Questions
Expect to be asked about specific scenarios related to PV audits and compliance. Think of examples from your past work where you successfully handled deviations or CAPA activities. This will demonstrate your problem-solving skills and ability to apply your knowledge in real situations.
✨Show Your Strategic Thinking
Since the role involves both operational and strategic support, be prepared to discuss how you approach risk assessments and management activities. Highlight any experiences where you’ve contributed to long-term strategies in pharmacovigilance, as this will set you apart from other candidates.
✨Be Ready to Discuss Remote Work
Given that the project can be performed largely remotely, be prepared to talk about your experience working in remote teams. Share how you maintain communication and collaboration with colleagues, especially when it comes to conducting audits and ensuring compliance.