At a Glance
- Tasks: Manage safety reports and maintain regulatory databases to ensure patient safety.
- Company: Join a leading pharmaceutical partner committed to compliance and innovation.
- Benefits: Gain valuable experience in a dynamic environment with potential for career growth.
- Other info: Collaborate with diverse teams and enhance your knowledge in pharmacovigilance.
- Why this job: Make a real difference in patient safety while developing your administrative skills.
- Qualifications: Strong organisational skills and attention to detail; proficiency in Microsoft Office required.
The predicted salary is between 30000 - 40000 £ per year.
SciPro is collaborating with one of our long-standing pharmaceutical partners to support a new search within the UK. We are searching for an organised administrator with excellent attention to detail and an interest in pharmacovigilance and regulatory affairs, to join the Clinical team.
The role will involve working closely with a range of internal teams and external partners, supporting compliance with regulatory requirements and contributing to patient safety.
Key responsibilities include:
- Managing customer safety and product quality reports, ensuring timely documentation and follow-up.
- Maintaining pharmacovigilance and regulatory databases and controlled documents.
- Preparing data and reports to support safety monitoring and trend analysis.
About you:
- Excellent written and verbal communication skills.
- Strong organisational skills with the ability to prioritise a varied workload.
- High level of accuracy and attention to detail.
- Proficient in Microsoft Office, particularly Word and Excel; database experience is advantageous.
- Previous experience in an administrative role within a regulated healthcare, pharmaceutical, or medical device environment.
PV and Medical Device Administrator employer: SciPro
At SciPro, we pride ourselves on being an exceptional employer, offering a dynamic work environment that fosters collaboration and innovation in the pharmaceutical sector. Our commitment to employee growth is evident through ongoing training opportunities and a supportive culture that values attention to detail and compliance, making it an ideal place for those passionate about pharmacovigilance and regulatory affairs. Located in the UK, our team enjoys a balanced work-life atmosphere while contributing to meaningful projects that enhance patient safety.
