At a Glance
- Tasks: Lead global Safety Pharmacology, shaping strategies from discovery to regulatory submission.
- Company: Global biopharmaceutical company with an innovative pipeline.
- Benefits: Competitive salary, leadership opportunities, and a chance to influence patient safety.
- Other info: Collaborative environment with opportunities for professional growth.
- Why this job: Make a real impact in drug development and mentor future talent.
- Qualifications: Significant experience in non-clinical drug development and strong leadership skills.
The predicted salary is between 80000 - 100000 £ per year.
Our client, a global biopharmaceutical company, is looking for a senior Safety Pharmacology leader to take ownership of the function across a broad and innovative pipeline. This is a critical function across the interface of discovery, non-clinical development, regulatory strategy, and patient safety. The successful candidate will shape safety pharmacology strategy from early discovery through to regulatory submission, while leading a global team and influencing key development decisions.
Key responsibilities- Lead the global Safety Pharmacology function, providing scientific, strategic, and operational direction.
- Develop safety pharmacology strategies to support discovery and development programmes across multiple therapeutic areas.
- Act as a senior scientific advisor to project teams, leadership, and governance committees.
- Oversee the design, interpretation, and regulatory reporting of non-clinical safety pharmacology studies.
- Drive the use of translational safety science, predictive toxicology, and emerging technologies to improve decision-making and reduce development risk.
- Work closely with Toxicology, DMPK, Clinical Pharmacology, Regulatory Affairs, Research, and Development teams.
- Represent the company externally with regulators, at scientific meetings, and through industry or academic collaborations.
- Build, mentor, and develop talent across the Safety Pharmacology team.
- Significant industry experience in non-clinical drug development, with strong leadership experience in Safety Pharmacology.
- Deep understanding of cardiovascular, respiratory, and CNS safety assessment.
- Strong knowledge of ICH S7A/S7B guidance and global regulatory expectations.
- Track record of supporting regulatory submissions and helping progress candidates from discovery into clinical development.
- Experience leading multidisciplinary teams in a global, matrixed environment.
Head of Safety Pharmacology in Slough employer: Barrington James
Join a leading global biopharmaceutical company that prioritises innovation and patient safety, offering a dynamic work environment where your expertise in Safety Pharmacology will directly influence the development of groundbreaking therapies. With a strong commitment to employee growth, you will have access to mentorship opportunities and the chance to lead a diverse team while collaborating with top professionals across various disciplines. Located in a vibrant area, the company fosters a culture of collaboration and scientific excellence, making it an exceptional place for those seeking meaningful and rewarding careers.
StudySmarter Expert Advice🤫
We think this is how you could land Head of Safety Pharmacology in Slough
✨Tip Number 1
Network like a pro! Reach out to industry contacts on LinkedIn or at conferences. We all know that sometimes it’s not just what you know, but who you know that can help you land that Head of Safety Pharmacology role.
✨Tip Number 2
Prepare for those interviews by brushing up on your knowledge of ICH S7A/S7B guidance and global regulatory expectations. We want you to be the go-to expert in the room, so practice articulating your experience in leading multidisciplinary teams.
✨Tip Number 3
Showcase your leadership skills! When discussing your past roles, highlight how you’ve built and mentored teams. We’re looking for someone who can inspire others and drive safety pharmacology strategies forward.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets seen by the right people. Plus, we love seeing candidates who are proactive about their job search.
We think you need these skills to ace Head of Safety Pharmacology in Slough
Some tips for your application 🫡
Tailor Your CV:Make sure your CV is tailored to the Head of Safety Pharmacology role. Highlight your relevant experience in non-clinical drug development and leadership in safety pharmacology. We want to see how your background aligns with our needs!
Craft a Compelling Cover Letter:Your cover letter is your chance to shine! Use it to explain why you're the perfect fit for this role. Share specific examples of how you've shaped safety pharmacology strategies and led teams in the past. We love a good story!
Showcase Your Knowledge:Demonstrate your understanding of ICH S7A/S7B guidance and global regulatory expectations in your application. We’re looking for someone who can hit the ground running, so let us know how you’ve navigated these areas before.
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, we love seeing candidates who take that extra step!
How to prepare for a job interview at Barrington James
✨Know Your Stuff
Make sure you brush up on your knowledge of safety pharmacology, especially in relation to cardiovascular, respiratory, and CNS assessments. Familiarise yourself with ICH S7A/S7B guidance and be ready to discuss how you've applied this in past roles.
✨Showcase Your Leadership Skills
As a senior role, they’ll want to see your leadership experience. Prepare examples of how you've built and mentored teams, and how you've influenced key decisions in a global, matrixed environment. Be ready to discuss specific challenges you faced and how you overcame them.
✨Connect the Dots
Demonstrate your ability to integrate safety pharmacology with other functions like Toxicology and Clinical Pharmacology. Think about how you can articulate your experience in driving cross-functional collaboration and improving decision-making through translational safety science.
✨Prepare for Regulatory Discussions
Since you'll be representing the company externally, prepare to discuss your experience with regulatory submissions. Have examples ready that highlight your success in navigating regulatory expectations and how you've contributed to progressing candidates from discovery into clinical development.
