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- Tasks: Assist in clinical trials, manage documents, and support research teams.
- Company: Premier Research, a global leader in clinical research and product development.
- Benefits: Flexible work environment, career growth, and the chance to make a real impact.
- Why this job: Join a mission-driven team transforming lives through innovative medical solutions.
- Qualifications: 5 years of clinical research experience and strong organisational skills.
- Other info: Dynamic team culture with opportunities for continuous learning and development.
The predicted salary is between 36000 - 60000 ÂŁ per year.
Premier Research is looking for a Clinical Trial Associate III to join our Functional Services Provider (FSP) team. You will help biotech, medtech, and specialty pharma companies transform life-changing ideas and breakthrough science into new medicines, devices, and diagnostics. What we do is profoundly connected to saving and improving lives, and we recognize our team members are the most valuable asset in delivering success.
We are here to help you grow, to give you the skills and opportunities to excel at work with the flexibility and balance your life requires. Your ideas influence the way we work, and your voice matters here. As an essential part of our team, you help us deliver the medical innovation that patients are desperate for. Join us and build your future here.
This CTA role will be working for our FSP business, and we require immediate availability to start. The role is offered as a fixed term contract with an anticipated end date of late November 2026.
What you’ll be doing:
- Assisting with eTMF (electronic Trial Master File) filing and administration on all studies including more complex studies
- Supporting the Clinical Research Associate (CRA) and site personnel with site level document collection
- Coordinating logistics and planning of meetings, events, and training
- Primary lead to disseminate announcements and training materials related to clinical system updates and enhancements, as required
- Co-Leads and participates in project team meetings, prepares meeting minutes, and maintains action/decision logs
- Creating, maintaining and providing quality checks for tracking tools and database repositories
- Performing Clinical Inspection Readiness and Quality Management System activities (e.g., deviations and CAPAs)
- Tracking non-TMF documents and study status
- Reporting document collection and tracking issues
- Maintaining and leading CTA team in clinical inspection readiness and supporting regulatory inspections and/or audits as required
What we’re searching for:
- 5 years clinical research “CTA-like” work and must include hands-on experience of audit preparation
- Exposure at working within a smaller company environment is essential
- Experience with CROs and vendors
- TMF experienced with workflows, document statuses, structure, compliance review
- Wingspan and Veeva experience will be considered as advantageous
- Study finance support activities
- Support metric reporting and compliance oversight meeting management including minutes, agenda, action items, etc.
Premier Research is more than a company – it’s a community furthering research to improve the lives of patients in critical need. We are a diverse staff thinking creatively, challenging ideas, and solving complex problems. Our Values – We Aim High, We Work Together, We Stay Agile, We Get It Done, We Care – mirror the determination, flexibility and trust that our team embodies. As a Premier team member, you have the power to make an impact, regardless of job title and location. Our dedication to biotech and specialty pharma is unlike any other. We provide our staff with innovative technologies and continuous learning.
Clinical Trial Associate III employer: Premier Research Group
Contact Detail:
Premier Research Group Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Clinical Trial Associate III
✨Tip Number 1
Network like a pro! Reach out to your connections in the clinical research field and let them know you're on the lookout for opportunities. You never know who might have a lead or can put in a good word for you.
✨Tip Number 2
Prepare for interviews by researching the company and its values. At Premier Research, they care about innovation and teamwork, so be ready to share how your experiences align with their mission and how you can contribute to their goals.
✨Tip Number 3
Practice your responses to common interview questions, especially those related to clinical trial processes and compliance. Being articulate about your experience with TMF and audit preparation will set you apart from the competition.
✨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 you’re genuinely interested in being part of the Premier Research community.
We think you need these skills to ace Clinical Trial Associate III
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to the Clinical Trial Associate III role. Highlight your relevant experience, especially in clinical research and any hands-on audit preparation you've done. We want to see how your skills align with what we do!
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you're passionate about clinical trials and how you can contribute to our mission at Premier Research. Keep it concise but impactful – we love a good story!
Showcase Your Team Spirit: We value collaboration, so don’t forget to mention your experience working in teams. Share examples of how you’ve contributed to group projects or supported colleagues in achieving common goals. We’re all about working together here!
Apply Through Our Website: For the best chance of getting noticed, apply directly through our website. It’s the easiest way for us to find your application and get back to you. Plus, it shows you’re serious about joining our team!
How to prepare for a job interview at Premier Research Group
✨Know Your Stuff
Make sure you brush up on your knowledge of clinical trial processes and the specific responsibilities of a Clinical Trial Associate III. Familiarise yourself with eTMF systems, audit preparation, and any relevant software like Wingspan and Veeva. This will show that you're not just interested in the role but also prepared to hit the ground running.
✨Showcase Your Experience
Be ready to discuss your previous experience in clinical research, especially any hands-on work with audit preparation and document management. Use specific examples to illustrate how you've contributed to past projects, particularly in smaller company environments, as this is essential for the role.
✨Emphasise Teamwork
Premier Research values collaboration, so be sure to highlight your ability to work well within a team. Share examples of how you've successfully coordinated with colleagues or supported site personnel in previous roles. This will demonstrate that you align with their core values of working together and caring for each other.
✨Prepare Questions
Have a few thoughtful questions ready to ask at the end of your interview. This could be about the company's approach to clinical inspections or how they support continuous learning for their staff. Asking questions shows your genuine interest in the role and helps you assess if the company is the right fit for you.