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- Tasks: Lead safety science and pharmacovigilance for drug development and post-marketing.
- Company: Join a dynamic global pharmaceutical company making a real impact.
- Benefits: Enjoy hybrid work options and a competitive salary.
- Why this job: Be at the forefront of drug safety, contributing to global health.
- Qualifications: Degree in healthcare/life sciences; experience in pharmacovigilance required.
- Other info: Must be eligible to work in the UK; reference job 140 666.
The predicted salary is between 43200 - 72000 £ per year.
CK Group are recruiting for a Director Safety Scientist, to join a growing global pharmaceutical company, on a permanent basis, in Welwyn, Hertfordshire, UK.
The Director Safety Scientist will require you to:
- Provide safety science and pharmacovigilance support across the drug development lifecycle, from early-phase trials to post-marketing.
- Develop and maintain a deep understanding of the safety profile of assigned products or therapy areas.
- Lead and contribute to signal detection and management activities.
- Oversee safety-related documents including CCDS, RMPs, REMS, DSURs, and PBRERs.
- Act as a key safety contributor on study teams and within global regulatory submissions (INDs, NDAs, MAAs, variations, renewals).
Further Responsibilities will include:
- Reviewing and medically assessing individual and aggregate case safety reports.
- Supporting labelling document updates and risk communication strategies.
- Participating in study teams and cross-functional safety discussions, including input on study protocols and post-authorization safety studies (PASS).
- Ensuring compliance with quality systems and applicable global regulations.
Your Background:
- A degree in a healthcare or life sciences discipline is required; a postgraduate qualification (e.g. MSc, PharmD, MD, PhD) is preferred.
- Significant experience in pharmacovigilance, clinical development, or medical affairs within the pharmaceutical industry.
- Strong understanding of GxP standards, global regulatory requirements, and safety reporting frameworks.
- Experience with signal management systems, regulatory safety submissions, and drug safety databases.
It is essential that applicants hold entitlement to work in the UK. Please quote job reference 140 666 in all correspondence.
Director Safety Scientist employer: New Scientist
Contact Detail:
New Scientist Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Director Safety Scientist
✨Tip Number 1
Network with professionals in the pharmaceutical industry, especially those involved in pharmacovigilance and safety science. Attend relevant conferences or webinars to meet potential colleagues and learn about the latest trends in drug safety.
✨Tip Number 2
Familiarise yourself with the specific safety reporting frameworks and regulations that are relevant to the role. This knowledge will not only help you in interviews but also demonstrate your commitment to understanding the complexities of the position.
✨Tip Number 3
Engage with online communities and forums related to pharmacovigilance and drug safety. Sharing insights and asking questions can help you build your reputation in the field and may lead to valuable connections.
✨Tip Number 4
Prepare to discuss your experience with signal detection and management during interviews. Be ready to provide examples of how you've contributed to safety-related documents and regulatory submissions in your previous roles.
We think you need these skills to ace Director Safety Scientist
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights relevant experience in pharmacovigilance and clinical development. Emphasise your understanding of GxP standards and any specific safety reporting frameworks you've worked with.
Craft a Strong Cover Letter: In your cover letter, explain why you are passionate about safety science and how your background aligns with the responsibilities of the Director Safety Scientist role. Mention specific experiences that demonstrate your leadership in safety-related activities.
Highlight Key Achievements: When detailing your work history, focus on key achievements related to signal detection, safety document oversight, and regulatory submissions. Use quantifiable results where possible to showcase your impact.
Proofread Your Application: Before submitting, carefully proofread your application for any spelling or grammatical errors. A polished application reflects your attention to detail, which is crucial in the pharmaceutical industry.
How to prepare for a job interview at New Scientist
✨Know Your Safety Science
Make sure you have a solid understanding of safety science and pharmacovigilance. Be prepared to discuss your experience with drug development lifecycles and how you've contributed to safety assessments in previous roles.
✨Familiarise Yourself with Regulatory Requirements
Brush up on GxP standards and global regulatory requirements relevant to the pharmaceutical industry. Being able to demonstrate your knowledge of safety reporting frameworks will show that you're well-prepared for the role.
✨Prepare for Scenario-Based Questions
Expect questions that assess your problem-solving skills in real-world scenarios. Think about past experiences where you led signal detection or managed safety-related documents, and be ready to share those examples.
✨Showcase Your Team Collaboration Skills
As a Director Safety Scientist, you'll need to work closely with cross-functional teams. Highlight your experience in collaborating with study teams and your contributions to safety discussions during interviews.
