At a Glance
- Tasks: Coordinate and manage clinical trials, ensuring high-quality data and patient care.
- Company: Join St Pancras Clinical Research, a leading UK Site Management Organisation.
- Benefits: Starting salary of £30,000, with opportunities for growth and development.
- Other info: Dynamic team environment in London with strict deadlines and exciting challenges.
- Why this job: Make a real difference in patients' lives while working on innovative clinical research.
- Qualifications: 1 year of clinical research experience and strong understanding of GCP required.
The predicted salary is between 30000 - 30000 £ per year.
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 London site.
About St Pancras Clinical Research
Established in 2016, St Pancras Clinical Research is a leading UK Site Management Organisation. 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. In addition, our clinical and scientific specialists offer wide-ranging and practical expert advice to sponsors on their drug development programmes, based upon substantial experience in the public, private, academic and commercial pharma fields.
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.
Location: London site (Barbican).
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 a high-pressure environment with strict targets and deadlines.
- Able to manage multiple projects with efficiency and produce high quality work.
Application deadline: 6th July 2026. 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.
Study Coordinator in Portsmouth employer: St Pancras Clinical Research
St Pancras Clinical Research is an exceptional employer, offering a vibrant work culture that prioritises patient care and professional development. Located in the heart of London, our team enjoys a collaborative environment with ample opportunities for growth within the clinical research field, supported by experienced specialists dedicated to advancing medical science. Join us to be part of meaningful clinical trials that make a real difference in patients' lives.
Contact Details:
St Pancras Clinical Research Recruitment Team
StudySmarter Expert Advice🤫
We think this is how you could land Study Coordinator in Portsmouth
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We think you need these skills to ace Study Coordinator in Portsmouth
Some tips for your application 🫡
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Tailor Your Documents to the Job:Don't use a one-size-fits-all approach! Make sure your CV and cover letter are specifically tailored for this role. Highlight any certifications you have relevant to health administration, and ensure you clearly connect your previous roles to the skills needed for the full-time position at St Pancras Clinical Research. This way, you're showing them you’ve done your homework and are genuinely interested in being a part of their team.
How to prepare for a job interview at St Pancras Clinical Research
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In health sciences administration, being organised is key. Make sure you can demonstrate your skills in managing schedules, paperwork, and data accurately. Be ready to discuss specific tools you've used, like electronic health record systems or scheduling software, and how they improved efficiency in your past experiences.
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