At a Glance
- Tasks: Lead and manage patient safety processes, ensuring compliance and quality in drug surveillance.
- Company: Join Sandoz, a leader in innovative healthcare solutions.
- Benefits: Competitive salary, diverse work environment, and opportunities for professional growth.
- Other info: Dynamic team culture focused on innovation and collaboration.
- Why this job: Make a real impact on patient safety and contribute to global health.
- Qualifications: Experience in pharmacovigilance, clinical trials, and strong leadership skills.
The predicted salary is between 60000 - 80000 £ per year.
Monitors and audits the company’s drug, biologics or medical devices surveillance program including the intake, evaluation, processing and follow-up on adverse reports. Participates in the resolution of any legal liability and in complying with government regulations. Ensures accurate receipt, maintenance and assessment against product labeling. Reports events or reactions as required by regulatory agencies including adverse events data from clinical trials, spontaneous or solicited sources, periodic and experience reports. May provide trending and safety signal detection and assessment. Supports all clinical trial activity and post marketing.
Major accountabilities:
- Global and/or regional, cross-functional leadership of assigned pharmacovigilance processes across Sandoz business units to ensure compliance with worldwide regulations with maximum efficiency.
- Globally responsible for compliance, quality, efficiency and management of Post Marketing and Clinical Trial adverse event handling.
- Lead management of activities/interfaces with other Global Line Functions management, Investigator Sites, Sandoz affiliates and Sandoz Sectors management to ensure timeliness, consistency and quality of safety information and to achieve a common understanding of other departmental needs.
- Build high performance safety teams with challenging clear objectives in alignment with Global functional objectives to facilitate implementation of strategic initiatives.
- Accountable for delivery of continuous operations (quality and compliance) goals.
- Optimize operational efficiency and clinical trial effectiveness by ensuring speedy follow-up for key safety information.
- Manage direct reports. Responsible for ensuring recruitment, development of top safety talent and retention of high performing associates to maintain stable pharmacovigilance operations.
- Ensure regular performance evaluations, development and succession planning.
- Manage audits and inspections. Takes complete responsibility for timely implementation of necessary corrective and preventive actions (CAPA commitments).
- Maintain inspection readiness at all times to minimize findings.
- Distribution of marketing samples (where applicable).
Key performance indicators:
- Adherence to Sandoz policy and guidelines.
- Project and stakeholder feedback.
- Operational risk mitigation and audit/inspection findings.
- Quality and timely reporting of KPI and safety reports/updates.
- Results of audits/inspections.
Minimum Requirements:
Work Experience: Critical Negotiations, People Challenges, Operations Management and Execution, Collaborating across boundaries, People Leadership.
Skills: Clinical Trial, Databases, Employee Training, Pharmacovigilance, Project Management, Reporting, Safety Science, Team Management.
Languages: English.
EEO Statement: Sandoz Group of Companies are Equal Opportunity Employers and take pride in maintaining a diverse environment. We do not discriminate in recruitment, hiring, training, promotion or other employment practices for reasons of race, color, religion, gender, national origin, age, sexual orientation, gender identity or expression, marital or veteran status, disability, or any other legally protected status. We are committed to building diverse teams, representative of the patients and communities we serve, and we strive to create an inclusive workplace that cultivates bold innovation through collaboration and empowers our people to unleash their full potential.
Accessibility and reasonable accommodations: Sandoz Group of Companies are committed to working with and providing reasonable accommodation to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please connect with us outlining the job requisition number in your message.
Salary Range Skills Desired: Clinical Trial, Databases, Employee Training, Pharmacovigilance, Reporting, Safety Science, Team Management, Waterfall Project Management.
Senior Patient Safety Manager employer: Sandoz
Contact Detail:
Sandoz Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Senior Patient Safety Manager
✨Tip Number 1
Network like a pro! Reach out to your connections in the industry, attend relevant events, and engage with professionals on platforms like LinkedIn. We all know that sometimes it’s not just what you know, but who you know that can help you land that Senior Patient Safety Manager role.
✨Tip Number 2
Prepare for interviews by researching the company and its culture. Understand their pharmacovigilance processes and be ready to discuss how your experience aligns with their needs. We want you to shine, so practice common interview questions and have your own questions ready to show your interest!
✨Tip Number 3
Showcase your skills! Create a portfolio or a presentation that highlights your achievements in clinical trials, safety science, and team management. We believe that demonstrating your expertise can set you apart from other candidates and make a lasting impression.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets noticed. Plus, we’re always looking for passionate individuals who are ready to contribute to our mission in patient safety. So, get your application in and let’s make a difference together!
We think you need these skills to ace Senior Patient Safety Manager
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to the Senior Patient Safety Manager role. Highlight your experience in pharmacovigilance and any relevant leadership roles you've held. We want to see how your skills align with our needs!
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you're passionate about patient safety and how your background makes you the perfect fit for our team. Keep it engaging and personal – we love a good story!
Showcase Your Achievements: When detailing your work experience, focus on specific achievements rather than just duties. Use metrics where possible to demonstrate your impact in previous roles. We’re all about results, so let us know how you’ve made a difference!
Apply Through Our Website: We encourage you to apply directly through our website. It’s the best way to ensure your application gets into the right hands. Plus, you’ll find all the info you need about the role and our company culture there!
How to prepare for a job interview at Sandoz
✨Know Your Stuff
Make sure you’re well-versed in pharmacovigilance processes and regulations. Brush up on the latest trends in patient safety and be ready to discuss how your experience aligns with the role's requirements.
✨Showcase Your Leadership Skills
As a Senior Patient Safety Manager, you'll need to demonstrate strong leadership abilities. Prepare examples of how you've built high-performance teams or managed cross-functional projects effectively in the past.
✨Be Ready for Scenario Questions
Expect questions that assess your problem-solving skills in real-world situations. Think about challenges you've faced in previous roles and how you resolved them, especially regarding compliance and quality management.
✨Ask Insightful Questions
Prepare thoughtful questions about the company’s approach to patient safety and their expectations for the role. This shows your genuine interest and helps you gauge if the company culture aligns with your values.