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For Companies At a Glance
- Tasks: Support regulatory submissions and manage clinical trial documentation.
- Company: Join Medpace, a leading clinical research organisation making a real impact.
- Benefits: Enjoy flexible work, competitive pay, and great career growth opportunities.
- Why this job: Be part of a mission to improve lives through innovative medical research.
- Qualifications: Bachelor's in Life Sciences and strong organisational skills required.
- Other info: Dynamic team environment with a focus on professional development.
The predicted salary is between 28800 - 43200 £ per year.
Our clinical operations activities are growing rapidly, and we are currently seeking a full-time, office-based Graduate to join our Clinical Operations team as an Entry Level Regulatory Submissions Coordinator. This position plays a key role in the clinical trial management process at Medpace. If you want an exciting career where you can develop and grow your career even further, then this is the opportunity for you.
Responsibilities
- Provide day-to-day departmental support activities to Regulatory Submissions Coordinators;
- Maintain database and spreadsheets as necessary to facilitate tracking and documentation of departmental activities;
- Collect, review, organize, and assemble regulatory start-up submissions;
- Perform other tasks as needed.
Additional Responsibilities
- Prepare, review, and file clinical trial applications;
- Communicate with research sites (hospitals, etc.) to collect all essential documents required before the site starts to enrol patients to participate in the clinical trial;
- Provide insightful input on regulatory submissions documents and maintain timelines for study start-up through both internal and external collaboration;
- Ensure submissions comply with applicable regulations and guidance documents.
Qualifications
- Bachelor's degree in a Life Sciences field;
- Interest in clinical trials;
- Knowledge of Microsoft® Office;
- Excellent organization and communication skills;
- Great attention to detail.
Medpace Overview
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.
What to Expect Next
A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps.
Entry Level Regulatory Submissions Coordinator in Stirling employer: Medpace
Contact Detail:
Medpace Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Entry Level Regulatory Submissions Coordinator in Stirling
✨Tip Number 1
Network like a pro! Reach out to people in the industry, attend events, and connect on LinkedIn. 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 researching Medpace and understanding their mission. Be ready to discuss how your skills align with their goals, especially in clinical trials and regulatory submissions.
✨Tip Number 3
Practice your communication skills! Since this role involves liaising with research sites, being clear and concise is key. Try mock interviews with friends or use online resources to sharpen your responses.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets seen. Plus, it shows you’re genuinely interested in joining the Medpace team.
We think you need these skills to ace Entry Level Regulatory Submissions Coordinator in Stirling
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, especially in clinical trials or life sciences, to show us you’re a great fit!
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to express your passion for clinical trials and how your background aligns with our mission at Medpace. Keep it concise but impactful!
Show Off Your Attention to Detail: Since this role requires great attention to detail, make sure your application is free from typos and errors. A polished application reflects your commitment to quality, which we value highly.
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 Stuff
Make sure you understand the basics of regulatory submissions and clinical trials. Brush up on key terms and processes that are relevant to the role. This will not only help you answer questions confidently but also show your genuine interest in the field.
✨Showcase Your Organisational Skills
Since this role requires excellent organisation, prepare examples from your past experiences where you successfully managed multiple tasks or projects. Be ready to discuss how you keep track of details and deadlines, as this will be crucial for the position.
✨Communicate Clearly
Effective communication is key in this role, especially when liaising with research sites. Practice articulating your thoughts clearly and concisely. You might even want to do a mock interview with a friend to refine your responses.
✨Ask Insightful Questions
Prepare thoughtful questions about the company and the role. This shows that you’re engaged and have done your homework. Ask about the team dynamics, the types of projects you might work on, or how success is measured in the role.
