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- Tasks: Support global clinical studies and ensure compliance with regulatory standards.
- Company: Join Advanced Clinical, a growing biopharmaceutical partner with a collaborative culture.
- Benefits: Fully remote work, exposure to global trials, and career growth opportunities.
- Why this job: Make a real impact in clinical research while working flexibly from anywhere.
- Qualifications: 2+ years in clinical research, strong understanding of GCP, and excellent communication skills.
- Other info: Be part of a high-performing team and contribute to innovative projects.
The predicted salary is between 36000 - 60000 £ per year.
Advanced Clinical is growing and we are looking to hire four Clinical Trial Specialists to join our Clinical Operations team. These roles will support an established biopharmaceutical partner through our FSP model and offer the chance to work on global clinical studies across multiple phases. This is a fully remote opportunity.
About the Role
As a Clinical Trial Specialist, you will work as a Coordinator, supporting moderately complex clinical studies and contributing to the successful planning, execution, and close-out of trials. You will work closely with the clinical trial team to ensure activities are conducted in accordance with GCP, SOPs, and regulatory standards.
Key Responsibilities
- Support activities for Phase 1–4 studies from feasibility and start-up through close-out
- Manage and track essential study and site documentation, ensuring completeness and TMF compliance.
- Assist the Study Lead in preparing clinical trial documents, site materials, and study manuals.
- Coordinate and document study meetings, including agenda preparation and minutes.
- Support study site oversight, including monitoring report review, site performance tracking, and issue escalation
- May perform co-monitoring or ad hoc site visits with oversight
- Assist with vendor coordination, deliverables tracking, and invoice review
- Participate in data review, query resolution, deviation assessments, and safety-related activities
- Collaborate cross-functionally with internal teams, CROs, and vendors to maintain study progress
Requirements
- Minimum of 2 years’ experience in clinical research (3 years preferred), ideally within pharma, biotech or CRO
- Previous experience in site monitoring or as a study coordinator is advantageous.
- Strong understanding of GCP, ICH guidelines, and the clinical development process
- Experience with electronic systems such as TMF, CTMS, Veeva Vault, SharePoint, or similar
- Proficient in Word, Excel, and PowerPoint, with strong communication and organisational skills
- Bachelor’s degree in a scientific or health-related discipline (or equivalent)
Why Join Advanced Clinical?
This opportunity offers remote work flexibility, exposure to global trials, and the opportunity to grow within a high-performing team working closely with an innovative sponsor. You will be part of a collaborative environment where your contributions will have an impact.
Clinical Trial Specialist in Bradford employer: Advanced Clinical
Contact Detail:
Advanced Clinical Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Clinical Trial Specialist in Bradford
✨Tip Number 1
Network like a pro! Reach out to your connections in the clinical research field, attend virtual events, and engage with professionals on LinkedIn. We all know that sometimes it’s not just what you know, but who you know that can help you land that Clinical Trial Specialist role.
✨Tip Number 2
Prepare for those interviews! Research the company and the specific trials they’re working on. We recommend practising common interview questions related to GCP and clinical trial processes so you can showcase your expertise confidently.
✨Tip Number 3
Showcase your skills! Create a portfolio or a presentation that highlights your previous experiences in clinical research. We love seeing how candidates have contributed to past studies, so don’t hold back on sharing your successes!
✨Tip Number 4
Apply through our website! It’s the best way to ensure your application gets noticed. We’re always on the lookout for passionate individuals ready to make an impact in clinical trials, so don’t hesitate to submit your application directly.
We think you need these skills to ace Clinical Trial Specialist in Bradford
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to the Clinical Trial Specialist role. Highlight your relevant experience in clinical research, especially any work with GCP and ICH guidelines. We want to see how your background aligns with what we're looking for!
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 your skills can contribute to our team. Keep it concise but engaging – we love a good story!
Showcase Your Skills: Don’t forget to showcase your technical skills, especially with electronic systems like TMF or CTMS. Mention your proficiency in Word, Excel, and PowerPoint too. We’re keen on seeing how you can hit the ground running!
Apply Through Our Website: We encourage you to apply through our website for a smoother application process. It’s the best way for us to receive your application directly and ensures you don’t miss out on any important updates from us!
How to prepare for a job interview at Advanced Clinical
✨Know Your Clinical Research Basics
Make sure you brush up on your knowledge of GCP, ICH guidelines, and the clinical development process. Being able to discuss these topics confidently will show that you’re not just familiar with the terms but understand their importance in the role.
✨Showcase Your Organisational Skills
As a Clinical Trial Specialist, you'll need to manage documentation and track study progress. Prepare examples from your past experience where you successfully organised complex information or coordinated multiple tasks. This will demonstrate your ability to handle the responsibilities of the role.
✨Familiarise Yourself with Relevant Tools
Get comfortable with electronic systems like TMF, CTMS, and Veeva Vault before the interview. If you have experience with these tools, be ready to discuss how you used them in previous roles. If not, do a bit of research to show your willingness to learn.
✨Prepare Questions for Your Interviewers
Interviews are a two-way street! Prepare thoughtful questions about the team dynamics, project timelines, or the company culture. This shows your genuine interest in the position and helps you assess if it’s the right fit for you.