At a Glance
- Tasks: Manage and process pharmacovigilance data to ensure patient safety.
- Company: Join Sanofi, a pioneering biopharma company focused on improving lives.
- Benefits: Hybrid working, competitive salary, and opportunities for professional growth.
- Other info: Collaborate with diverse teams and drive innovation in healthcare.
- Why this job: Make a real impact in drug development and patient safety.
- Qualifications: Life science degree or health professional with relevant experience.
The predicted salary is between 35000 - 45000 £ per year.
Location: Reading, UK
Job Type: 9-month Fixed-Term Contract
Working Arrangements: Hybrid - 3 days per week on-site in Reading and 2 days remote
As a Patient Safety and Pharmacovigilance Officer, you'll provide accurate and timely processing and management of all Pharmacovigilance (PV) data to contribute to an efficient pharmacovigilance service. You'll ensure Medical and Safety Officers and Pharmacovigilance Managers are informed in a timely and accurate fashion of potential safety, quality, and regulatory issues, while assisting in the overall evaluation of pharmacovigilance data and identification of potential safety signals.
Main responsibilities:
- Manage and process pharmacovigilance data accurately and on time, including PV inbox, individual and aggregate reports, SUSAR management, safety agreements, local literature monitoring, reconciliation, quality checks, and local risk management activities
- Support the MSO/PVM in the preparation and maintenance of PV documentation, including clinical and post-authorisation studies, patient support programmes, digital and market research programmes
- Monitor and document safety data regularly to identify trends, clusters, and potential safety issues, and respond promptly to queries from corporate or health authorities
- Maintain and update PV procedures in line with current regulations and global company policies, supporting training, compliance activities, and corrective and preventative actions
- Foster timely and accurate communication with Business Unit functions under the guidance of the MSO/PVM or Senior PV Officer
- Manage PV administrative tasks, maintaining comprehensive hard copy and electronic files, ensuring all processes and data are always inspection and audit ready
- Uphold ethical and safety standards, taking personal accountability for ethics and governance knowledge while actively contributing to a safe working environment
About you
- Life science degree or Qualified Health Professional (e.g., pharmacist, pharmacy technician, nurse) with previous relevant experience in Drug Safety, PV, pharmacy, nursing, or medicine
- Good understanding of PV principles with strong attention to detail and familiarity with computer systems for word processing and database management
- Strong oral and written communication skills, with the ability to share knowledge openly, align around shared goals and collaborate effectively across teams
- Aim Higher mindset - you set high standards, move with urgency, and focus on what matters to deliver impact for patients and stakeholders
- Bold and decisive - you seize opportunities, embrace change, and use technology and fresh thinking to drive innovation
- Patient-first commitment - you integrate patient perspectives into everything you do, never compromising on integrity, quality, safety, and compliance
- Lead Together spirit - you build trust, celebrate wins, create space for diverse voices, and provide real-time feedback to drive continuous improvement
Why choose us?
- Be part of a pioneering biopharma company that engages patients early in drug development and uses their insights to design studies that reflect real-world needs.
- Work at the forefront of drug discovery, harnessing cutting-edge AI, data, and digital platforms to push the boundaries of science.
- Help improve the lives of millions of people globally by making drug development quicker and more effective.
- Enjoy opportunities to collaborate beyond your area of expertise, working with diverse teams across science, clinical, and digital fields to spark new ideas and drive breakthroughs.
We are proud to be a Disability Confident Employer, committed to offering interviews to candidates who request consideration under the Scheme and meet the minimum requirements for this role. If you have a disability and require adjustments for the interview process, please email us at diversity.recruitmentUKIE@sanofi.com. We are dedicated to ensuring an inclusive and supportive experience for all applicants.
Patient Safety and Pharmacovigilance Officer in Reading employer: Sanofi
Sanofi is an exceptional employer that champions innovation and collaboration in the biopharma sector, offering a hybrid working model that promotes work-life balance. With a strong commitment to employee growth, you will have the opportunity to engage in cutting-edge research while contributing to meaningful advancements in patient safety and pharmacovigilance. Located in Reading, UK, our inclusive work culture fosters diverse perspectives and encourages continuous improvement, making it a rewarding place to build your career.
StudySmarter Expert Advice🤫
We think this is how you could land Patient Safety and Pharmacovigilance Officer in Reading
✨Get Familiar with Temporary Roles in Pharma
Temporary positions in the pharmaceutical industry often arise during specific periods, like product launches or seasonal hiring sprints. Keep an eye on timelines and be proactive in reaching out to companies, especially around these busy times!
✨Join Pharma Networking Events
Participate in local and virtual pharmaceutical networking events or job fairs. This is a fantastic way to get in front of hiring managers and learn more about temporary opportunities directly from those in the know.
✨Leverage Your University Career Services
If you’re a student or recent grad, tap into your university’s career services which often have specific connections to pharma companies looking to fill temporary roles. They might even have exclusive internship programmes that lead to temp jobs!
✨Be Visible Online and Offline
Utilise platforms like LinkedIn to share your interests in temporary roles and connect with industry professionals. Plus, consider writing about relevant pharmaceutical topics to showcase your knowledge and enthusiasm—this can help you stand out to hiring companies like Sanofi.
We think you need these skills to ace Patient Safety and Pharmacovigilance Officer in Reading
Some tips for your application 🫡
Highlight Your Relevant Experience:In the pharmaceutical industry, it's crucial to showcase any relevant experience you have, whether it's internships, lab work, or coursework. Let’s emphasise your familiarity with drug development processes and any hands-on experience you've had with lab equipment or clinical trials in your CV.
Mention Certifications and Training:If you’ve got any certifications relevant to pharmaceuticals, like Good Clinical Practice (GCP) or a certification in pharmacovigilance, make sure to include them. These show your commitment to the field and can make a positive impact on your application for a temporary role at Sanofi.
Show Your Flexibility and Availability:Temporary positions often require immediate availability and flexibility in working hours. In your cover letter, make it clear when you can start and your ability to adapt to changing schedules, as this is key to a successful application.
Express Your Learning Goals:Since this is a temporary role, we suggest discussing what you hope to learn or gain from the experience at Sanofi. This not only shows your eagerness but also helps employers see you as someone who’s ready to make the most out of the opportunity.
How to prepare for a job interview at Sanofi
✨Know Your Regulations
In the pharmaceutical industry, it’s crucial to understand key regulations like GMP (Good Manufacturing Practices) or GCP (Good Clinical Practices). Brush up on these standards and be ready to discuss how they influence your work approach during your interview with Sanofi.
✨Emphasise Adaptability
Since this is a temporary role, show that you're ready to hit the ground running. Share examples from your past experiences that demonstrate your ability to adapt quickly to new environments or changes, especially in a fast-paced setting like pharmaceuticals.
✨Highlight Relevant Skills and Tools
Whether it’s laboratory techniques or software like LabWare or SAS, make sure you can confidently talk about your technical skills. If you have experience with any specific tools used in previous roles, relate that directly to how it can help Sanofi achieve its goals.
✨Prepare for Technical Questions
Be ready for technical questions related to drug development processes or quality assurance. We should expect scenarios where you might have to troubleshoot a problem or suggest improvements on a project—this shows your problem-solving capability in a temporary role.
