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- Tasks: Coordinate and manage clinical trials, ensuring patient care and data quality.
- Company: Join St Pancras Clinical Research, a leading Site Management Organisation in the UK.
- Benefits: Starting salary of £30,000 p.a. with opportunities for growth and development.
- Why this job: Make a real difference in patients' lives while advancing your career in clinical research.
- Qualifications: Minimum 1 year experience in clinical research and strong understanding of GCP.
- Other info: Dynamic team environment with a focus on high-quality work and patient-centric practices.
The predicted salary is between 24000 - 42000 £ per year.
Join to apply for the Study Coordinator role at St Pancras Clinical Research. Due to continued growth and expansion, St Pancras Clinical Research is looking to recruit an experienced Study Coordinator to join our dynamic team at our Eastbourne site.
About St Pancras Clinical Research: Established in 2016, St Pancras Clinical Research is a London-based Site Management Organisation with three sites in the UK - London, Chester and Eastbourne. We conduct Phase II and III clinical trials with new medicines, for patients with various chronic diseases. Our experience includes chronic pain and memory disorders resulting from inflammatory, neurological and neurodegenerative conditions, as well as diabetes and dermatology.
Job Description: The Study Coordinator will be responsible at St Pancras Clinical Research Ltd (SPCR) for the day-to-day coordination and administration of all aspects of our ongoing clinical trials, as regulated by the research protocols (approved by the Research Ethics Committees of the UK Health Regulatory Authority (HRA) & the Medicines and Healthcare products Regulatory Agency (MHRA), Good Clinical Practice (GCP) guidelines and supporting legislation, while abiding by SPCR’s Policies and Standard Operating Practices. The Study Coordinator will work within the Clinical Team to ensure the successful delivery of research at SPCR.
Responsibilities:
- Managing all aspects of your allocated clinical trials, including patient visit management, data management and pharmacy activities.
- Working alongside the clinical team to deliver timely, efficient and high-quality clinical trial data.
- Ensuring the highest standard of care for our patients.
- Performing all tasks relating to the clinical trials in strict adherence to the trial protocols.
- Performing administrative tasks of any kind relating to clinical trials.
- Laboratory work.
- Assisting with patient recruitment.
Salary: starting at £30,000 p.a.; dependent upon experience.
Requirements:
- 1 year minimum clinical research coordinator experience in CTIMPs.
- A strong understanding and practical experience of ICH Good Clinical Practice (GCP).
- Patient-centric approach to clinical and research practice.
- Flexible and can do attitude.
- IT literate - experience of Microsoft Office applications; electronic databases; and data entry systems.
Qualities St Pancras Clinical Research are looking for: team player; diligent and high level of attention to detail; willing to work in high pressure environment with strict targets and deadlines; and able to manage multiple projects with efficiency and produce high quality work.
This vacancy may close before the current listed closing date. You are advised not to delay submitting your completed application. Any applicants submitted after the deadline will not be considered.
Application Process Information: Please note due to the high number of applicants we will only be able to provide feedback for those invited to the interview stage. If you do not hear back from us after 3 weeks of your application being submitted, then unfortunately your application has been unsuccessful.
Seniority level: Mid-Senior level
Employment type: Full-time
Job function: Research, Analyst, and Information Technology
Industries: Research Services
Study Coordinator in Eastbourne employer: St Pancras Clinical Research
Contact Detail:
St Pancras Clinical Research Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Study Coordinator in Eastbourne
✨Tip Number 1
Network like a pro! Reach out to your connections in the clinical research field, attend industry events, and join relevant online groups. You never know who might have the inside scoop on job openings or can put in a good word for you.
✨Tip Number 2
Prepare for interviews by researching St Pancras Clinical Research and understanding their work. Familiarise yourself with their clinical trials and be ready to discuss how your experience aligns with their needs. Show them you’re not just another candidate!
✨Tip Number 3
Practice makes perfect! Conduct mock interviews with friends or family to build your confidence. Focus on articulating your experience in clinical trials and how you can contribute to their team’s success.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets seen. Plus, it shows you’re genuinely interested in joining our dynamic team at St Pancras Clinical Research.
We think you need these skills to ace Study Coordinator in Eastbourne
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to the Study Coordinator role. Highlight your relevant experience in clinical trials and any specific 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 St Pancras Clinical Research. Keep it engaging and personal.
Showcase Your Attention to Detail: As a Study Coordinator, attention to detail is key. Make sure your application is free from typos and errors. We appreciate candidates who take the time to present their best work right from the start!
Apply Through Our Website: We encourage you to apply directly through our website. It’s the easiest way for us to receive your application and ensures you’re considered for the role. Don’t miss out on this opportunity!
How to prepare for a job interview at St Pancras Clinical Research
✨Know Your Stuff
Make sure you brush up on your knowledge of Good Clinical Practice (GCP) and the specific clinical trials that St Pancras Clinical Research conducts. Being able to discuss these topics confidently will show that you're serious about the role and understand the industry.
✨Show Your Team Spirit
As a Study Coordinator, you'll be working closely with a clinical team. Be prepared to share examples of how you've successfully collaborated in the past. Highlighting your ability to work as part of a team will resonate well with the interviewers.
✨Demonstrate Your Attention to Detail
Given the nature of clinical trials, attention to detail is crucial. Bring examples of how you've managed multiple projects or tasks while maintaining high-quality work. This will help illustrate your diligence and capability to handle the responsibilities of the role.
✨Ask Smart Questions
Prepare thoughtful questions about the company and the role. Inquire about their current trials, patient recruitment strategies, or how they ensure compliance with regulations. This shows your genuine interest and helps you assess if the company is the right fit for you.
