Freelance/Contract Pharmacovigilance Consultant - PV QA/Auditing in Telford
Freelance/Contract Pharmacovigilance Consultant - PV QA/Auditing

Freelance/Contract Pharmacovigilance Consultant - PV QA/Auditing in Telford

Telford Freelance 36000 - 60000 £ / year (est.) No home office possible
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ProPharma

At a Glance

  • Tasks: Conduct PV audits, ensure compliance, and support risk management activities.
  • Company: ProPharma, a leading RCO improving health for 20 years.
  • Benefits: Remote work flexibility with one trip to the Benelux region.
  • Other info: Embrace innovation and collaboration in a supportive environment.
  • Why this job: Join a diverse team making a real impact in pharmacovigilance.
  • Qualifications: BSc in life sciences and extensive PV experience 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

Experience required

  • 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 Telford employer: ProPharma

ProPharma is an exceptional employer that champions diversity, equity, and inclusion, fostering a collaborative and innovative work culture. With a commitment to employee growth and a holistic approach to professional development, team members are empowered to thrive in their roles while contributing to meaningful advancements in healthcare. The flexibility of remote work combined with the opportunity for occasional travel to the Benelux region makes this role particularly appealing for those seeking a dynamic and rewarding consulting experience.
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 Telford

✨Network Like a Pro

Get out there and connect with folks in the industry! Attend webinars, join LinkedIn groups, or even hit up local meetups. The more people you know, the better your chances of landing that freelance gig.

✨Show Off Your Skills

When you're chatting with potential clients, make sure to highlight your experience in PV QA and auditing. Share specific examples of how you've tackled challenges in the past. This will help them see you as the go-to expert they need!

✨Be Ready to Adapt

Freelancing means flexibility! Be prepared to adjust your approach based on client needs. Whether it's jumping into a new project or adapting to different regulations, showing that you can pivot will make you stand out.

✨Apply Through Our Website

Don't forget to check out our website for the latest opportunities! Applying directly through us not only streamlines the process but also shows your commitment to working with our team. Let's get you that contract!

We think you need these skills to ace Freelance/Contract Pharmacovigilance Consultant - PV QA/Auditing in Telford

Pharmacovigilance
PV Quality Assurance
PV Auditing
Risk Management
Regulatory Compliance
Deviation Management
CAPA Activities
Risk Assessments
Life-Sciences Knowledge
Operational Support
Strategic Support
Fluency in English
Remote Work Capability
Collaboration Skills

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, it helps us keep everything organised!

How to prepare for a job interview at ProPharma

✨Know Your Pharmacovigilance Inside Out

Make sure you brush up on your knowledge of pharmacovigilance regulations and practices. Be prepared to discuss specific auditing techniques and risk management strategies you've used in the past. This will show that you’re not just familiar with the field, but that you can actively contribute to their projects.

✨Showcase Your Experience

Prepare examples from your previous roles that highlight your experience in PV QA and auditing. Use the STAR method (Situation, Task, Action, Result) to structure your answers. This will help you articulate your contributions clearly and demonstrate your problem-solving skills.

✨Understand Their Needs

Research ProPharma and their clients to understand their specific challenges in pharmacovigilance. Tailor your responses to show how your skills can directly address these needs. This shows initiative and a genuine interest in the role.

✨Be Ready for Remote Work Questions

Since the project is largely remote, be prepared to discuss your experience with remote work. Highlight your communication skills and how you manage tasks independently. This will reassure them that you can thrive in a flexible working environment.

Freelance/Contract Pharmacovigilance Consultant - PV QA/Auditing in Telford
ProPharma
Location: Telford
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