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- Tasks: Collect and track serious adverse events while ensuring compliance in clinical trials.
- Company: Join a leading clinical contract research organisation in Stirling.
- Benefits: Enjoy competitive pay, flexible work, and opportunities for professional growth.
- Why this job: Make a real difference in patient safety and contribute to groundbreaking clinical research.
- Qualifications: Bachelor's degree in life sciences and 2+ years in Clinical Trial Pharmacovigilance.
- Other info: Be part of a multidisciplinary team in a dynamic and supportive environment.
The predicted salary is between 36000 - 60000 £ per year.
A clinical contract research organization is seeking a Clinical Safety Coordinator in Stirling. In this role, you will collect and track serious adverse events, generate safety narratives, and ensure compliance throughout clinical trials, working within a multidisciplinary team.
The ideal candidate has a Bachelor's degree in life sciences and 2+ years in Clinical Trial Pharmacovigilance.
Medpace offers a competitive compensation package and professional growth opportunities in a flexible work environment.
Pharmacovigilance Safety Specialist — Clinical Trials in Stirling employer: Medpace
Contact Detail:
Medpace Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Pharmacovigilance Safety Specialist — Clinical Trials in Stirling
✨Tip Number 1
Network like a pro! Reach out to professionals in the pharmacovigilance field on LinkedIn or at industry events. We can’t stress enough how valuable personal connections can be in landing that Clinical Safety Coordinator role.
✨Tip Number 2
Prepare for those interviews! Research common questions related to clinical trials and pharmacovigilance. We recommend practising your answers with a friend or even in front of the mirror to boost your confidence.
✨Tip Number 3
Showcase your skills! When you get the chance, highlight your experience with serious adverse events and compliance during interviews. We want to see how your background aligns with the role and how you can contribute to the team.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets noticed. Plus, we often have exclusive opportunities listed there that you won’t find anywhere else.
We think you need these skills to ace Pharmacovigilance Safety Specialist — Clinical Trials in Stirling
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights your experience in Clinical Trial Pharmacovigilance. We want to see how your background aligns with the role, so don’t be shy about showcasing relevant skills and achievements!
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you’re passionate about pharmacovigilance and how your experience makes you a great fit for our team. Keep it engaging and personal!
Showcase Your Team Spirit: Since this role involves working within a multidisciplinary team, let us know about your collaborative experiences. Share examples of how you’ve successfully worked with others to achieve common goals in clinical trials.
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’s super easy!
How to prepare for a job interview at Medpace
✨Know Your Pharmacovigilance Basics
Make sure you brush up on your knowledge of pharmacovigilance principles and practices. Be ready to discuss serious adverse events and how they are tracked, as well as the importance of compliance in clinical trials.
✨Showcase Your Experience
Prepare specific examples from your past roles that highlight your experience in Clinical Trial Pharmacovigilance. Discuss any challenges you faced and how you overcame them, as this will demonstrate your problem-solving skills and adaptability.
✨Understand the Company Culture
Research the clinical contract research organisation you're interviewing with. Understanding their values and work environment will help you tailor your responses and show that you’re a good fit for their multidisciplinary team.
✨Ask Insightful Questions
Prepare thoughtful questions to ask at the end of your interview. Inquire about their approach to safety narratives or how they ensure compliance during trials. This shows your genuine interest in the role and helps you assess if it’s the right fit for you.
