At a Glance
- Tasks: Coordinate clinical trials and ensure timely delivery of project tasks with precision.
- Company: Join a growing UK team in a dynamic clinical research environment.
- Benefits: Enjoy flexible work, competitive pay, and great career growth opportunities.
- Other info: Be part of a supportive culture with employee appreciation events and wellness initiatives.
- Why this job: Make a real impact in healthcare while working on exciting international studies.
- Qualifications: 1-3 years in clinical trials and a degree in Life Sciences required.
The predicted salary is between 30000 - 40000 € per year.
Due to continuous business growth and a strong study pipeline, we are looking for Project Coordinators to join our successful and growing UK team and engage in clinical trial management on a day-to-day level, with the opportunity to work on international studies across oncology, cardiology, rare diseases and more. This position will work with our operational teams to accomplish tasks and projects that are instrumental to the company's success. Seeking dedicated people who are willing to invest a number of years to Project Coordination before moving on to their next role.
Please submit a cover letter to support your application.
Responsibilities- Work closely with the Project Clinical Trial Manager for timely delivery of recurrent tasks consistently with a high degree of accuracy;
- Compile and maintain project-specific status reports within the Clinical Trial Management System (CTMS);
- Interact with the internal project team, Sponsor, study sites, and third-party vendors;
- Ownership of the Trial Master File;
- Create and maintain project timelines and enrolment projections;
- Coordinate project meetings and produce quality minutes.
- 1-3 years of clinical trials experience;
- Bachelor's or Master's Degree in Life Sciences;
- Excellent oral and written English Language communication skills;
- Knowledge of Microsoft Office programs;
- Experience in a health sciences or business setting preferred;
- Excellent organisational and prioritisation skills;
- Strong attention to detail.
- 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.
Clinical Project Coordinator in London employer: Medpace, Inc.
As a Clinical Project Coordinator in our London office, you will be part of a dynamic and supportive team dedicated to advancing clinical trials across various therapeutic areas. We pride ourselves on fostering a flexible work environment that prioritises employee well-being and professional development, offering structured career paths and numerous opportunities for growth. Join us to contribute to meaningful projects while enjoying competitive compensation and a culture that values your contributions.
StudySmarter Expert Advice🤫
We think this is how you could land Clinical Project Coordinator in London
✨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 the company and its projects. Show genuine interest in their work, especially in areas like oncology or cardiology. Tailor your responses to highlight how your experience aligns with their needs.
✨Tip Number 3
Practice makes perfect! Conduct mock interviews with friends or use online resources. This will help you articulate your thoughts clearly and confidently when it’s your turn to shine.
✨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 Clinical Project Coordinator in London
Some tips for your application 🫡
Craft a Compelling Cover Letter:Your cover letter is your chance to shine! Make sure to highlight your relevant experience in clinical trials and how it aligns with the role. We want to see your passion for project coordination and how you can contribute to our team.
Showcase Your Attention to Detail:In this role, accuracy is key. When writing your application, double-check for any typos or errors. We appreciate candidates who take the time to ensure their submissions are polished and professional.
Tailor Your CV to the Role:Don’t just send out the same CV for every job. Tailor it to highlight your experience in clinical trials and project management. We love seeing how your skills match what we’re looking for in a Clinical Project Coordinator.
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 you’re serious about joining our team!
How to prepare for a job interview at Medpace, Inc.
✨Know Your Clinical Trials
Make sure you brush up on your knowledge of clinical trials, especially in oncology, cardiology, and rare diseases. Being able to discuss recent developments or challenges in these areas will show your genuine interest and expertise.
✨Master the Job Description
Take a close look at the job description and align your experiences with the responsibilities listed. Be ready to provide specific examples of how you've successfully managed projects or worked with teams in previous roles.
✨Prepare for Team Dynamics
Since you'll be interacting with various stakeholders, think about how you can demonstrate your teamwork skills. Prepare anecdotes that highlight your ability to collaborate effectively with internal teams, sponsors, and vendors.
✨Showcase Your Organisational Skills
As a Project Coordinator, organisation is key. Bring examples of how you've maintained project timelines or status reports in the past. You might even want to prepare a mock project timeline to discuss during the interview!
