Find a job 
Featured Companies 
Featured Universities 
For Companies At a Glance
- Tasks: Oversee regulatory submissions and site activations for clinical trials.
- Company: Leading clinical research organisation in the UK with a collaborative culture.
- Benefits: Competitive salary, professional development, and impactful work.
- Why this job: Make a real difference in clinical research timelines and outcomes.
- Qualifications: Bachelor’s degree and 6+ years in regulatory affairs and study start-up.
- Other info: Dynamic environment with opportunities for career advancement.
The predicted salary is between 48000 - 72000 £ per year.
A clinical research organization in the United Kingdom is seeking a Study Start-up Associate Senior to oversee regulatory submissions and site activations for clinical trials. The ideal candidate will possess a Bachelor’s degree and over 6 years of experience in regulatory affairs and study start-up across multiple countries. Strong communication skills and knowledge of local regulations are essential for this role. This position offers the opportunity to significantly impact clinical research timelines and outcomes in a collaborative environment.
Senior Study Start-Up & Regulatory Lead employer: Emmes Group
Contact Detail:
Emmes Group Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Senior Study Start-Up & Regulatory Lead
✨Tip Number 1
Network like a pro! Reach out to your connections in the clinical research field and let them know you're on the hunt for a Senior Study Start-Up & Regulatory Lead role. You never know who might have the inside scoop on job openings or can put in a good word for you.
✨Tip Number 2
Prepare for interviews by brushing up on local regulations and recent trends in clinical trials. We want you to be the go-to expert in the room, so practice articulating how your experience aligns with the role's requirements. Confidence is key!
✨Tip Number 3
Don’t just apply anywhere; focus on organisations that resonate with your values and career goals. Use our website to find roles that excite you and tailor your approach to each one. Quality over quantity, folks!
✨Tip Number 4
Follow up after interviews! A quick thank-you email can go a long way in leaving a positive impression. It shows your enthusiasm for the role and keeps you fresh in their minds as they make their decision.
We think you need these skills to ace Senior Study Start-Up & Regulatory Lead
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights your experience in regulatory affairs and study start-up. We want to see how your skills align with the role, so don’t be shy about showcasing your achievements!
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 Senior Study Start-Up & Regulatory Lead position. Share specific examples of your past work that relate to the job description.
Showcase Communication Skills: Since strong communication skills are essential for this role, make sure to demonstrate these in your application. Whether it’s through your writing style or by mentioning relevant experiences, let us know you can communicate effectively!
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 Emmes Group
✨Know Your Regulations
Make sure you brush up on local regulations and compliance standards relevant to clinical trials. Being able to discuss specific regulations and how they impact study start-up will show your expertise and readiness for the role.
✨Showcase Your Experience
Prepare to share detailed examples from your past roles that highlight your experience in regulatory submissions and site activations. Use the STAR method (Situation, Task, Action, Result) to structure your responses and make them impactful.
✨Communicate Clearly
Strong communication skills are a must for this position. Practice articulating complex regulatory concepts in simple terms, as you may need to explain these to team members or stakeholders who aren't as familiar with the details.
✨Demonstrate Collaboration
Since this role involves working in a collaborative environment, be ready to discuss how you've successfully worked with cross-functional teams in the past. Highlight any experiences where your collaboration led to improved timelines or outcomes in clinical research.
