International Regulatory Affairs Lead - Submissions & Strategy in Salisbury
International Regulatory Affairs Lead - Submissions & Strategy

International Regulatory Affairs Lead - Submissions & Strategy in Salisbury

Salisbury Full-Time 48000 - 72000 £ / year (est.) No home office possible
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At a Glance

  • Tasks: Lead regulatory compliance and manage submissions for international markets.
  • Company: Global pharmaceutical company focused on innovation and compliance.
  • Benefits: Competitive salary, health benefits, and opportunities for professional growth.
  • Why this job: Make a significant impact in global healthcare by ensuring regulatory success.
  • Qualifications: BSc in relevant sciences and 10+ years in Regulatory Affairs.
  • Other info: Collaborative environment with diverse teams and exciting projects.

The predicted salary is between 48000 - 72000 £ per year.

A global pharmaceutical company is seeking an Associate Director of Regulatory Affairs to lead regulatory compliance for international markets. The role includes managing regulatory submissions, representing the regulatory team in launch activities, and collaborating across various functions.

Candidates should have a BSc in relevant sciences and at least 10 years in Regulatory Affairs, with strong communication and project management skills.

International Regulatory Affairs Lead - Submissions & Strategy in Salisbury employer: KalVista Pharmaceuticals

As a leading global pharmaceutical company, we pride ourselves on fostering a dynamic and inclusive work environment that encourages innovation and collaboration. Our employees benefit from comprehensive professional development opportunities, competitive compensation packages, and a strong commitment to work-life balance, all while contributing to meaningful projects that impact global health. Join us in our state-of-the-art facilities, where your expertise in regulatory affairs will be valued and your career can thrive.
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Contact Detail:

KalVista Pharmaceuticals Recruiting Team

StudySmarter Expert Advice 🤫

We think this is how you could land International Regulatory Affairs Lead - Submissions & Strategy in Salisbury

✨Tip Number 1

Network like a pro! Reach out to professionals in the regulatory affairs field on LinkedIn or at industry events. We can’t stress enough how valuable personal connections can be in landing that dream job.

✨Tip Number 2

Prepare for interviews by brushing up on your knowledge of international regulations and compliance. We recommend practising common interview questions with a friend or mentor to boost your confidence.

✨Tip Number 3

Showcase your project management skills during interviews. We all know that managing submissions is key, so be ready to discuss specific examples where you’ve successfully led projects in the past.

✨Tip Number 4

Don’t forget to apply through our website! It’s the best way to ensure your application gets noticed. Plus, we love seeing candidates who are proactive about their job search.

We think you need these skills to ace International Regulatory Affairs Lead - Submissions & Strategy in Salisbury

Regulatory Compliance
Regulatory Submissions
Communication Skills
Project Management
Collaboration
BSc in Relevant Sciences
International Market Knowledge
Leadership Skills
Strategic Thinking
Problem-Solving Skills

Some tips for your application 🫡

Tailor Your CV: Make sure your CV highlights your experience in Regulatory Affairs, especially any international submissions you've managed. We want to see how your background aligns with the role, so don’t be shy about showcasing your relevant skills!

Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you're the perfect fit for the International Regulatory Affairs Lead position. Share specific examples of your project management and communication skills that relate to the job description.

Showcase Your Teamwork: Since collaboration is key in this role, highlight any experiences where you’ve worked across different functions or teams. We love to see how you can bring people together to achieve regulatory success!

Apply Through Our Website: We encourage you to apply directly through our website. It’s the best way for us to receive your application and ensures you’re considered for the role. Plus, it shows us you’re keen on joining our team!

How to prepare for a job interview at KalVista Pharmaceuticals

✨Know Your Regulatory Stuff

Make sure you brush up on the latest international regulatory guidelines and compliance standards. Being able to discuss recent changes or trends in the industry will show that you're not just experienced, but also proactive and knowledgeable.

✨Showcase Your Project Management Skills

Prepare examples of how you've successfully managed regulatory submissions and projects in the past. Use the STAR method (Situation, Task, Action, Result) to structure your responses, highlighting your ability to lead teams and meet deadlines.

✨Communicate Clearly and Confidently

Since strong communication is key for this role, practice articulating your thoughts clearly. Consider doing mock interviews with a friend or using video tools to refine your delivery and ensure you come across as confident and engaging.

✨Collaborate Like a Pro

Be ready to discuss how you've worked with cross-functional teams in previous roles. Share specific instances where your collaboration led to successful outcomes, demonstrating your ability to work well with others and drive results in a team setting.

International Regulatory Affairs Lead - Submissions & Strategy in Salisbury
KalVista Pharmaceuticals
Location: Salisbury

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