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- Tasks: Coordinate global clinical studies and collaborate with international teams.
- Company: Leading Clinical Research Organization with a focus on innovative medical therapies.
- Benefits: Competitive salary, flexible working, and professional development opportunities.
- Why this job: Transition from academia to impactful clinical research in a dynamic environment.
- Qualifications: PhD in Life Sciences and strong communication skills required.
- Other info: Fast-tracked career growth and exposure to international projects.
The predicted salary is between 28800 - 48000 £ per year.
A leading Clinical Research Organization (CRO) is seeking candidates with PhDs and/or Post-Doctoral Research experience for a full-time, office-based Associate Clinical Trial Manager (aCTM) position within its Clinical Trial Management team.
This position is available across several key European locations — London, Munich, Milan, and Madrid — offering candidates the opportunity to work in a highly collaborative and international environment.
This is an excellent opportunity for recent PhD graduates to transition from academia into the clinical research and drug development industry, applying strong analytical and scientific skills to the management and coordination of global clinical studies. The successful candidate will receive comprehensive training, gain exposure to international projects, and have the potential for fast-tracked career development into Clinical Trial Management (CTM).
Key Responsibilities
- Collaborate on global study activities, working closely with Project Coordinators and Clinical Trial Managers to ensure operational excellence.
- Maintain accurate and timely project documentation and status reports within the Clinical Trial Management System (CTMS).
- Communicate effectively with internal stakeholders, Sponsors, study sites, and third-party vendors.
- Support regulatory and quality control processes, ensuring full compliance with SOPs and ICH-GCP standards.
- Manage study supplies, timelines, and deliverables in line with project milestones.
- Coordinate and facilitate project meetings, including agenda preparation and production of meeting minutes.
- Contribute to maintaining high-quality documentation and process efficiency across assigned studies.
Qualifications
- PhD in Life Sciences (or a related scientific field).
- Excellent communication and presentation skills, with fluency in English.
- Strong organizational, analytical, and problem-solving capabilities.
- Ability to thrive in a fast-paced, global, and team-oriented environment.
- Prior experience in the CRO, pharmaceutical, or biotechnology sector is beneficial but not essential.
About the Company
This organization is a global, full-service Clinical Research Organization (CRO) supporting Phase I–IV clinical development for biotechnology, pharmaceutical, and medical device clients. Its mission is to accelerate the development of innovative, safe, and effective medical therapies through scientific rigor, operational discipline, and cross-functional collaboration.
With operations spanning 40+ countries and therapeutic expertise in oncology, cardiology, CNS, metabolic, and infectious diseases, the company is committed to advancing clinical research and improving patient outcomes worldwide.
Why Join
- Locations: London, Munich, Milan, and Madrid
- Competitive compensation and benefits package
- Flexible, hybrid working model
- Structured training and professional development pathways
- Inclusive, collaborative international culture
- Company-sponsored recognition and wellness initiatives
Neuroscience PhD Clinical Trial Coordinator employer: Meet Life Sciences
Contact Detail:
Meet Life Sciences Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Neuroscience PhD Clinical Trial Coordinator
✨Network Like a Pro
Get out there and connect with professionals in the clinical research field. Attend conferences, webinars, or local meetups to meet people who can help you land that dream role. Remember, it’s all about who you know!
✨Ace the Informational Interview
Don’t be shy about reaching out for informational interviews. These chats can give you insider knowledge about the industry and might even lead to job opportunities. Plus, it shows your genuine interest in the field!
✨Showcase Your Skills
When you get the chance to interview, make sure to highlight your analytical and problem-solving skills. Use examples from your PhD or post-doc experience to demonstrate how you can contribute to the team’s success.
✨Apply Through Our Website
We encourage you to apply directly through our website for the best chance at landing the role. It shows initiative and gives you a direct line to the hiring team. Don’t miss out on this opportunity!
We think you need these skills to ace Neuroscience PhD Clinical Trial Coordinator
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to highlight your PhD and any relevant research experience. We want to see how your skills align with the role of a Clinical Trial Coordinator, so don’t be shy about showcasing your analytical and organisational abilities!
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you’re excited about transitioning from academia to clinical research. We love seeing genuine enthusiasm and how you can contribute to our collaborative environment.
Showcase Your Communication Skills: Since effective communication is key in this role, make sure your application reflects your ability to convey complex ideas clearly. Whether it’s through your CV or cover letter, we want to see that you can engage with various stakeholders effortlessly.
Apply Through Our Website: We encourage you to apply directly through our website for a smoother process. It helps us keep track of applications and ensures you get all the latest updates about your application status. Plus, it’s super easy!
How to prepare for a job interview at Meet Life Sciences
✨Know Your Science
Brush up on your neuroscience knowledge and be ready to discuss how your PhD or post-doctoral research relates to clinical trials. Be prepared to explain complex concepts in simple terms, as you may need to communicate with non-scientific stakeholders.
✨Showcase Your Organisational Skills
Since the role involves managing timelines and project documentation, come prepared with examples of how you've successfully organised projects in the past. Highlight any tools or systems you used to keep everything on track.
✨Practice Your Communication
Effective communication is key in this role. Practice articulating your thoughts clearly and concisely. You might even want to do a mock interview with a friend to get comfortable discussing your experiences and answering questions.
✨Understand the Company Culture
Research the organisation's values and mission. Be ready to discuss how your personal values align with theirs, especially regarding collaboration and patient outcomes. This shows that you're not just interested in the job, but also in being part of their team.