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- Tasks: Coordinate high-quality clinical trials and engage with participants in a fast-paced environment.
- Company: Join a leading clinical research organisation focused on innovative health solutions.
- Benefits: Competitive salary, flexible hours, and opportunities for professional growth.
- Other info: Dynamic role with opportunities to work across Greater Manchester and diverse communities.
- Why this job: Make a real difference in healthcare while working on impactful IBS studies.
- Qualifications: Experience in clinical research coordination and strong organisational skills required.
The predicted salary is between 30000 - 36000 £ per year.
The Clinical Research Study Coordinator will play a key role in supporting the delivery of high-quality clinical trials focused on IBS across Leigh. Based within EMS’ mobile and fixed-site research infrastructure, you will be responsible for coordinating study operations, participant engagement, and ensuring smooth study delivery in line with protocols and regulatory requirements. This role offers an exciting opportunity to work on a high-profile IBS study while contributing to a broader range of EMS clinical research activities.
The ideal candidate will have prior experience coordinating clinical research studies and be confident working independently in a fast-paced, participant-focused setting.
Location: Leigh
Contract: Permanent
Monday-Friday: 37.5 hour week
Salary range: £30K-£36K depending on experience
Main Duties:
- Coordinate day-to-day operational aspects of assigned clinical studies, ensuring alignment with protocols, GCP, and EMS SOPs.
- Schedule and manage participant visits, including screening, enrolment, and follow-up activities.
- Maintain detailed, accurate study documentation, including source data, CRFs, logs, and regulatory binders.
- Collaborate with clinical staff, including nurses and investigators, to ensure study timelines and objectives are met.
- Support participant retention and compliance through effective communication and follow-up.
- Assist in the setup and maintenance of study equipment, supplies, and site readiness.
- Liaise with the data management team to ensure timely entry, verification, and query resolution.
- Participate in site meetings, staff training, monitoring visits, and audits as required.
- Ensure participant safety, confidentiality, and adherence to ethical and regulatory standards.
- Contribute to continuous improvement and operational excellence across the EMS Study portfolio.
Experience - Essential:
- Experience coordinating or supporting clinical research studies in an NHS, academic, or commercial setting.
- Understanding of ICH-GCP and regulatory frameworks governing clinical trials.
- Demonstrated ability to manage participant interactions and study workflows.
- Strong organisational skills with the ability to manage competing priorities.
- Confident using electronic data capture systems or clinical databases.
Experience - Preferable:
- Experience working in obesity, metabolic health, or lifestyle-related trials.
- Familiarity with community-based or mobile clinical research delivery models.
- Prior experience working with underserved or diverse populations.
Key Skills:
- Excellent written and verbal communication.
- Detail-oriented with a focus on data integrity and participant safety.
- Flexible and proactive team player.
- Strong time management and problem-solving skills.
- Technologically proficient, especially with study software and electronic documentation tools.
Other Requirements:
- Full UK residency and right to work.
- Valid UK driving licence and willingness to travel across Greater Manchester and EMS sites as needed.
- Flexibility to work early mornings, evenings, or weekends depending on study needs.
Clinical Research Study Coordinator in Leigh employer: EMS Healthcare
Contact Detail:
EMS Healthcare Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Clinical Research Study Coordinator in Leigh
✨Tip Number 1
Network like a pro! Reach out to your connections in the clinical research field, attend relevant events, and engage with professionals on platforms like LinkedIn. You never know who might have the inside scoop on job openings or can refer you directly.
✨Tip Number 2
Prepare for interviews by researching the company and understanding their current studies, especially those related to IBS. Tailor your responses to highlight how your experience aligns with their needs, showing that you're not just another candidate but the right fit for their team.
✨Tip Number 3
Practice makes perfect! Conduct mock interviews with friends or mentors to refine your answers and boost your confidence. Focus on articulating your past experiences in coordinating clinical studies and how they relate to the role you're applying for.
✨Tip Number 4
Don’t forget to follow up after interviews! A simple thank-you email reiterating your interest in the position can leave a lasting impression. And remember, apply through our website for the best chance at landing that Clinical Research Study Coordinator role!
We think you need these skills to ace Clinical Research Study Coordinator in Leigh
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to the Clinical Research Study Coordinator role. Highlight your experience in coordinating clinical studies and any relevant skills that match the job description. We want to see how you fit into our team!
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you're passionate about clinical research and how your background makes you the perfect fit for this role. We love seeing enthusiasm and a personal touch!
Showcase Your Organisational Skills: Since this role involves managing multiple tasks, be sure to highlight your organisational skills in your application. Share examples of how you've successfully juggled competing priorities in past roles. We appreciate a well-organised candidate!
Apply Through Our Website: Don't forget to apply through our website! It’s the best way for us to receive your application and ensures you’re considered for the role. Plus, it gives you a chance to explore more about what we do at StudySmarter!
How to prepare for a job interview at EMS Healthcare
✨Know Your Stuff
Make sure you brush up on your knowledge of clinical research protocols, GCP guidelines, and the specifics of IBS studies. Being able to discuss these topics confidently will show that you're serious about the role and understand what it entails.
✨Showcase Your Experience
Prepare to share specific examples from your past roles where you've successfully coordinated clinical studies. Highlight your organisational skills and how you've managed participant interactions, as this is crucial for the Clinical Research Study Coordinator position.
✨Engage with the Interviewers
Don’t just answer questions; engage in a conversation. Ask insightful questions about the study operations and participant engagement strategies they use. This shows your interest and helps you gauge if the company culture aligns with your values.
✨Demonstrate Flexibility
Be ready to discuss how you handle competing priorities and adapt to changing situations. Share examples of times when you had to be flexible in your approach, especially in fast-paced environments, as this role requires a proactive mindset.