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- Tasks: Coordinate regulatory submissions and support clinical development projects.
- Company: Join Medpace, a leading clinical research organisation making a real impact.
- Benefits: Enjoy flexible work, competitive pay, and great PTO packages.
- Why this job: Be part of a mission that improves lives through innovative medical solutions.
- Qualifications: Strong organisational skills and a passion for healthcare.
- Other info: Opportunities for professional growth in a supportive environment.
The predicted salary is between 21600 - 36000 £ per year.
Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, employing more than 5,000 people across 40+ countries.
Why Medpace?
- People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today.
- The work we’ve done over the past 30+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas.
- The work we do today will improve the lives of people living with illness and disease in the future.
Medpace Perks:
- Flexible work environment
- Competitive compensation and benefits package
- Competitive PTO packages
- Structured career paths with opportunities for professional growth
- Company-sponsored employee appreciation events
- Employee health and wellness initiatives
Awards:
- Recognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023 and 2024
- Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility
Entry Level Regulatory Submissions Coordinator in London employer: Medpace
Contact Detail:
Medpace Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Entry Level Regulatory Submissions Coordinator in London
✨Tip Number 1
Network like a pro! Reach out to people in the industry, attend events, and connect with Medpace employees on LinkedIn. Building relationships can open doors that applications alone can't.
✨Tip Number 2
Prepare for interviews by researching Medpace's mission and values. Show us how your passion aligns with our purpose of making a difference in patients' lives. Tailor your answers to reflect our commitment to quality and expertise.
✨Tip Number 3
Practice makes perfect! Conduct mock interviews with friends or mentors to boost your confidence. Focus on articulating your skills and experiences that relate to regulatory submissions and clinical development.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets noticed. Plus, it shows us you’re genuinely interested in joining the Medpace team.
We think you need these skills to ace Entry Level Regulatory Submissions Coordinator in London
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to the Entry Level Regulatory Submissions Coordinator role. Highlight any relevant experience or skills that align with the job description, and don’t forget to showcase your passion for the industry!
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to tell us why you’re excited about the role and how your background makes you a great fit. Keep it concise but engaging – we want to see your personality!
Showcase Your Attention to Detail: As a Regulatory Submissions Coordinator, attention to detail is key. Make sure your application is free from typos and errors. A polished application shows us you’re serious about the position and understand the importance of accuracy.
Apply Through Our Website: We encourage you to apply through our website for the best chance of getting noticed. It’s super easy, and you’ll be able to track your application status. Plus, we love seeing applications come directly from our site!
How to prepare for a job interview at Medpace
✨Know Your Stuff
Before the interview, dive deep into Medpace's mission and values. Understand their role in clinical research and how they impact patient lives. This knowledge will not only impress your interviewers but also help you connect your own goals with theirs.
✨Showcase Your Skills
As an Entry Level Regulatory Submissions Coordinator, highlight any relevant coursework or projects you've completed. Be ready to discuss how your skills can contribute to the regulatory process and ensure compliance. Use specific examples to demonstrate your understanding of regulatory submissions.
✨Ask Smart Questions
Prepare thoughtful questions about the company culture, team dynamics, and growth opportunities. This shows your genuine interest in the role and helps you assess if Medpace is the right fit for you. Questions about their recent projects or future goals can spark engaging conversations.
✨Practice Makes Perfect
Conduct mock interviews with friends or family to build confidence. Focus on articulating your thoughts clearly and concisely. Practising common interview questions related to regulatory submissions will help you feel more prepared and less anxious on the big day.
