Study Coordinator // UK based
Study Coordinator // UK based

Study Coordinator // UK based

Birmingham Freelance Home office possible
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At a Glance

  • Tasks: Coordinate clinical research studies and support patient-level activities remotely.
  • Company: Hobson Prior, a leading life sciences recruiter with a global reach.
  • Benefits: Flexible part-time hours, remote work, and valuable experience in clinical research.
  • Why this job: Make a real difference in patients' lives while gaining hands-on experience in clinical research.
  • Qualifications: Strong organisational skills and familiarity with clinical research processes required.
  • Other info: Contract for 58 months with less than 10% travel; start date December 2025.

Hobson Prior is seeking two Study Coordinators to join on a part-time, freelance basis. This remote role, based in the UK, involves supporting clinical research studies by coordinating patient-level activities and ensuring high-quality study delivery. You will act as a central point of contact for research sites, patients, and study teams, focusing on patient-centric practices and maintaining data integrity.

Please note that to be considered for this role you must have the right to work in this location.

Responsibilities:

  • Guide patients through the informed consent process and ensure compliance with ethical standards.
  • Schedule and manage assessments, logistics, and communication between patients, investigators, and other study-related entities.
  • Maintain accurate study documentation and input data into relevant systems.
  • Coordinate site and patient activities throughout the study lifecycle.
  • Monitor and report adverse events (AEs) and serious adverse events (SAEs).
  • Perform quality checks to ensure data accuracy and process compliance.
  • Support query resolution and ensure timely data entry into electronic systems.
  • Build strong relationships with patients, investigators, and research teams to enhance the study experience.
  • Manage daily tasks, prioritize work, and suggest solutions for complex issues.
  • Ensure ongoing inspection readiness and adherence to training requirements.

Key Skills and Requirements:

  • Proficiency in English (native level).
  • Strong organizational, communication, and time management skills.
  • Familiarity with clinical research processes, medical terminology, and patient safety reporting.
  • Ability to navigate and troubleshoot clinical technologies.
  • Professionalism and problem-solving skills to address escalations and provide solutions.
  • Knowledge of data collection best practices and strategies to minimize queries.
  • Understanding of clinical development processes and site activation.

Additional Details:

  • Contract Duration: 58 months.
  • Hours: 51 hours per month across all projects.
  • Start Date: December 2025.
  • Travel: Less than 10%, with occasional planned travel.

For more information, please contact Terrah-Leigh Pietersen.

If you are interested in applying to this exciting opportunity, then please click \’Apply\’ or to speak to one of our specialists visit the \’Contact Us\’ page.

Hobson Prior is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Hobson Prior is acting as an Employment Agency in relation to this vacancy.

By submitting this application, you confirm that you\’ve read and understood our privacy policy, which informs you how we process and safeguard your data – https://www.hobsonprior.com/privacy-policy.

Study Coordinator // UK based employer: Hobson Prior

Hobson Prior is an excellent employer for those seeking meaningful and rewarding work in the life sciences sector. With a strong focus on patient-centric practices and a commitment to high-quality study delivery, employees benefit from a supportive remote work culture that fosters professional growth and collaboration. The company offers flexible part-time opportunities, ensuring a healthy work-life balance while contributing to impactful clinical research.
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Contact Detail:

Hobson Prior Recruiting Team

StudySmarter Expert Advice 🤫

We think this is how you could land Study Coordinator // UK based

✨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 virtual interviews by setting up a distraction-free zone. Make sure your tech is working, and practice answering common questions related to study coordination. We want you to shine!

✨Tip Number 3

Showcase your skills! During interviews, highlight your organisational and communication abilities. Share specific examples of how you've managed patient interactions or data integrity in past roles.

✨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 serious about joining the team and ready to dive into the world of clinical research.

We think you need these skills to ace Study Coordinator // UK based

Organizational Skills
Communication Skills
Time Management Skills
Clinical Research Processes
Medical Terminology
Patient Safety Reporting
Data Integrity
Problem-Solving Skills
Quality Assurance
Data Collection Best Practices
Clinical Technologies Navigation
Relationship Building
Compliance with Ethical Standards
Monitoring Adverse Events

Some tips for your application 🫡

Tailor Your Application: Make sure to customise your CV and cover letter for the Study Coordinator role. Highlight your relevant experience in clinical research and patient management, as this will show us that you understand what we're looking for.

Showcase Your Skills: We want to see your strong organisational and communication skills shine through. Use specific examples from your past experiences to demonstrate how you've successfully managed tasks and built relationships in a professional setting.

Be Clear and Concise: When writing your application, keep it straightforward and to the point. We appreciate clarity, so avoid jargon and make sure your key points stand out. This will help us quickly see why you're a great fit!

Apply Through Our Website: Don't forget to apply directly through our website! This ensures your application gets to us without any hiccups. Plus, it shows us you're keen and ready to join our team at StudySmarter.

How to prepare for a job interview at Hobson Prior

✨Know Your Stuff

Make sure you brush up on clinical research processes and medical terminology. Familiarity with patient safety reporting and data collection best practices will show that you're serious about the role and can hit the ground running.

✨Showcase Your Organisational Skills

As a Study Coordinator, you'll need to juggle multiple tasks. Prepare examples of how you've managed your time effectively in previous roles. Highlight any experience you have with scheduling and coordinating activities, as this will be key in your interview.

✨Communicate Clearly

Strong communication is essential for this role. Practice articulating your thoughts clearly and concisely. You might even want to prepare a few questions to ask the interviewer about their patient-centric practices to demonstrate your interest.

✨Be Ready to Problem-Solve

Expect questions that assess your problem-solving skills. Think of scenarios where you've had to resolve issues or handle escalations. Showing that you can think on your feet and provide solutions will set you apart from other candidates.

Study Coordinator // UK based
Hobson Prior
Location: Birmingham
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