At a Glance
- Tasks: Coordinate global clinical studies and collaborate with international teams.
- Company: Leading Clinical Research Organization with a mission to improve patient outcomes.
- Benefits: Competitive salary, flexible working, and professional development opportunities.
- Other info: Fast-tracked career growth and exposure to international projects.
- Why this job: Transition from academia to impactful clinical research in a dynamic environment.
- Qualifications: PhD in Life Sciences and strong communication skills required.
The predicted salary is between 36000 - 60000 £ per year.
Neuroscience PhD Clinical Trial Coordinator
Direct message the job poster from Meet Life Sciences
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
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Neuroscience PhD Clinical Trial Coordinator employer: Meet Life Sciences
As a Market Access Consultant with our client, you will be part of a dynamic team that values innovation and collaboration in the evolving healthcare landscape. The company offers a supportive work culture with opportunities for professional growth, including mentoring junior team members and leading impactful projects. With competitive compensation, hybrid working options, and comprehensive benefits, this role provides a meaningful opportunity to contribute to the expansion of European Value & Access capabilities while enjoying a fulfilling work-life balance.
StudySmarter Expert Advice🤫
We think this is how you could land Neuroscience PhD Clinical Trial Coordinator
✨Unlock Networking Opportunities
Dive into industry-specific events like pharmaceutical conferences and seminars, where you can meet hiring managers from companies like Meet Life Sciences. These are goldmines for making connections and learning about job openings before they hit the mainstream job boards.
✨Join Relevant Professional Bodies
Get involved with organisations such as the Royal Pharmaceutical Society or your local pharmaceutical professionals' network. Being an active member can boost your credibility and may even lead to job referrals in top organisations like Meet Life Sciences.
✨Leverage Internships for Full-time Roles
If you can, consider pursuing internships in the pharmaceutical industry, especially with companies like Meet Life Sciences. These opportunities often pave the way for full-time positions and allow you to demonstrate your capabilities firsthand.
✨Tailor Your Approach
When you're applying for roles, don't rush it! Take the time to customise your applications for specific positions, showcasing relevant skills and experiences that align with what Meet Life Sciences is looking for. A tailored application can really make you stand out!
We think you need these skills to ace Neuroscience PhD Clinical Trial Coordinator
Some tips for your application 🫡
Showcase Your Relevant Experience:When applying for a role in the pharmaceutical industry, it's crucial to highlight any relevant experience you have. Whether that's internships, lab work, or even related coursework, make sure to weave this into your CV and cover letter. We want to see how your background aligns with the role you're applying for at Meet Life Sciences!
Emphasise Your Understanding of Regulations:The pharmaceutical industry is heavily regulated, so it's important to indicate your familiarity with industry standards and regulations. In your cover letter, mention any training or certifications you've received that are relevant, or discuss projects where you’ve navigated compliance. This will show Meet Life Sciences that you're not just a fit for the job but also a safety-conscious candidate!
Tailor Your CV to Be Result-Driven:Craft your CV to highlight quantifiable achievements, especially if you have previous roles in pharmaceuticals or related fields. Use metrics to demonstrate your impact, such as improved processing times or successful project completions while working on trials. This analytical approach will resonate well with hiring managers at Meet Life Sciences!
Convey Your Passion for the Industry:In your cover letter, express why you are passionate about working in the pharmaceutical sector. Whether it’s your desire to contribute to groundbreaking drug research or improve patient outcomes, let it shine through! At Meet Life Sciences, we value candidates who are truly enthusiastic about their work—you might just stand out from the crowd.
How to prepare for a job interview at Meet Life Sciences
✨Understand the Science
Make sure you brush up on key pharmaceutical concepts and recent developments in the industry. You might get asked some technical questions during the interview at Meet Life Sciences that show your grasp of drug development processes or regulatory requirements, so be ready to discuss them clearly.
✨Showcase Relevant Experience
If you have any hands-on experience or internships in a laboratory setting, be sure to highlight these in your responses. Think about the projects you worked on, the methodologies you used, and the impact you made. It's all about telling a story that connects your background to the role you're applying for.
✨Know Their Products
Take some time to familiarise yourself with Meet Life Sciences’s product range and recent breakthroughs. Understanding their portfolio not only shows your enthusiasm for the role but also allows you to ask insightful questions that demonstrate your interest in actively contributing to their projects.
✨Be Ready for Regulatory Scenarios
In a full-time pharmaceutical role, understanding the regulatory landscape is crucial. Prepare for situational questions that may test your problem-solving skills concerning compliance and safety standards. You could be asked how you'd handle a hypothetical issue regarding a drug’s market release, so think through your approach.
