At a Glance
- Tasks: Lead product safety evaluations and drive risk management strategies for innovative products.
- Company: Join a leading global company focused on product safety and innovation.
- Benefits: Attractive salary, health benefits, remote work options, and opportunities for professional growth.
- Other info: Dynamic role with opportunities for mentorship and continuous improvement.
- Why this job: Make a real impact on product safety and collaborate with industry experts.
- Qualifications: Experience in safety science, strong analytical skills, and ability to work cross-functionally.
The predicted salary is between 80000 - 100000 £ per year.
Product-level safety ownership
- Perform and lead signal detection, evaluation, validation and escalation activities for assigned product(s).
- Set the strategy for safety signal detection methodology, signal tracking and oversight of safety signals for assigned products.
- Drive, perform and document benefit risk evaluations and ensure appropriate risk management strategies are implemented.
- Lead and perform assessments for the preparation, review and approval of key safety deliverables (e.g. PSURs, DSURs, RMPs, regulatory responses).
- Translate safety data insights into actionable recommendations for product level benefit-risk discussions and regulatory interactions.
- Lead the clinical safety science interactions with partner companies for the assigned products (if applicable) ensuring sharing of safety information per the SDEA and the set up and collaborative functioning of the JSMT.
- Provide safety scientific input to ISS Evaluation Committee as required.
- In case of product quality escalations, work cross functionally to understand impacts on patients, and (if required) lead the preparation of a medical impact Health Hazard Assessment statement.
Cross-functional execution (MDT)
- Act as the Safety Science representative in the Medical Development Team (MDT) and ensure integration of safety into product development and lifecycle decisions.
- Provide clinical safety input into study design, conduct, analysis and interpretation, including study level Safety Lead responsibilities where applicable.
- Provide medical and pharmacovigilance expertise e.g. for the clinical safety strategy of the product clinical development program, the development of the Target Product Profile (TPP), the development and maintenance of the RSI, including IB and CDS Governance and decision-making.
- Chair product level Benefit Risk Teams (BRTs) and ensure effective operation per SOPs.
- Represent the BRT at Benefit Risk Council (BRC).
- Serve as the primary decision-maker for product-level safety issues, including signal validation and escalation.
Collaboration and delivery
- Lead interactions with external partners and service providers related to assigned product safety deliverables.
- Support regulatory interactions, inspections and audits at product level.
People and capability development
- Mentor colleagues and support capability development within the product safety team.
Continuous improvement & data-driven decision making
- Actively use and continuously develop proficiency in safety systems, data visualization tools, and AI enabled analyses (e.g. Veeva Vault(s), analytics dashboards) to support robust and efficient signal detection, safety assessments, and decision making for assigned products.
- Identify opportunities for process, data and system improvements within Safety Science.
Level of autonomy: works independently with accountability for assigned products, escalating complex or cross product issues as appropriate.
Global Product Safety Science Lead in Cambridge employer: Doist
Brink's is an exceptional employer that fosters a collaborative and innovative work culture, empowering employees to drive global commercial strategies in the ATM lifecycle solutions sector. With a strong focus on professional development and growth opportunities, employees are encouraged to expand their skills while contributing to sustainable growth and operational excellence. Located in a dynamic environment, Brink's offers unique advantages such as a diverse team and the chance to build long-term partnerships with global customers, making it a rewarding place to advance your career.
StudySmarter Expert Advice🤫
We think this is how you could land Global Product Safety Science Lead in Cambridge
✨Unlock Networking Opportunities
Dive into industry-specific events like pharmaceutical conferences and seminars, where you can meet hiring managers from companies like Doist. These are goldmines for making connections and learning about job openings before they hit the mainstream job boards.
✨Join Relevant Professional Bodies
Get involved with organisations such as the Royal Pharmaceutical Society or your local pharmaceutical professionals' network. Being an active member can boost your credibility and may even lead to job referrals in top organisations like Doist.
✨Leverage Internships for Full-time Roles
If you can, consider pursuing internships in the pharmaceutical industry, especially with companies like Doist. These opportunities often pave the way for full-time positions and allow you to demonstrate your capabilities firsthand.
✨Tailor Your Approach
When you're applying for roles, don't rush it! Take the time to customise your applications for specific positions, showcasing relevant skills and experiences that align with what Doist is looking for. A tailored application can really make you stand out!
We think you need these skills to ace Global Product Safety Science Lead in Cambridge
Some tips for your application 🫡
Showcase Your Relevant Experience:When applying for a role in the pharmaceutical industry, it's crucial to highlight any relevant experience you have. Whether that's internships, lab work, or even related coursework, make sure to weave this into your CV and cover letter. We want to see how your background aligns with the role you're applying for at Doist!
Emphasise Your Understanding of Regulations:The pharmaceutical industry is heavily regulated, so it's important to indicate your familiarity with industry standards and regulations. In your cover letter, mention any training or certifications you've received that are relevant, or discuss projects where you’ve navigated compliance. This will show Doist that you're not just a fit for the job but also a safety-conscious candidate!
Tailor Your CV to Be Result-Driven:Craft your CV to highlight quantifiable achievements, especially if you have previous roles in pharmaceuticals or related fields. Use metrics to demonstrate your impact, such as improved processing times or successful project completions while working on trials. This analytical approach will resonate well with hiring managers at Doist!
Convey Your Passion for the Industry:In your cover letter, express why you are passionate about working in the pharmaceutical sector. Whether it’s your desire to contribute to groundbreaking drug research or improve patient outcomes, let it shine through! At Doist, we value candidates who are truly enthusiastic about their work—you might just stand out from the crowd.
How to prepare for a job interview at Doist
✨Understand the Science
Make sure you brush up on key pharmaceutical concepts and recent developments in the industry. You might get asked some technical questions during the interview at Doist that show your grasp of drug development processes or regulatory requirements, so be ready to discuss them clearly.
✨Showcase Relevant Experience
If you have any hands-on experience or internships in a laboratory setting, be sure to highlight these in your responses. Think about the projects you worked on, the methodologies you used, and the impact you made. It's all about telling a story that connects your background to the role you're applying for.
✨Know Their Products
Take some time to familiarise yourself with Doist’s product range and recent breakthroughs. Understanding their portfolio not only shows your enthusiasm for the role but also allows you to ask insightful questions that demonstrate your interest in actively contributing to their projects.
✨Be Ready for Regulatory Scenarios
In a full-time pharmaceutical role, understanding the regulatory landscape is crucial. Prepare for situational questions that may test your problem-solving skills concerning compliance and safety standards. You could be asked how you'd handle a hypothetical issue regarding a drug’s market release, so think through your approach.
