Study Coordinator

Study Coordinator

London Full-Time 24000 - 42000 £ / year (est.) No home office possible
S

At a Glance

  • Tasks: Coordinate and manage clinical trials, ensuring patient care and data quality.
  • Company: Join St Pancras Clinical Research, a leading site management organisation in London since 2016.
  • Benefits: Competitive salary starting at £30,000, with opportunities for growth and development.
  • Why this job: Be part of impactful research that improves lives while working in a dynamic team environment.
  • Qualifications: Minimum 1 year experience in clinical research; strong understanding of GCP required.
  • Other info: Application deadline is 16th July 2025; apply early as positions may close sooner.

The predicted salary is between 24000 - 42000 £ per year.

Job Description

Job Title: Study Coordinator

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 London-based 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.

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.
  • 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 high pressure environment with strict targets and deadlines; and able to manage multiple projects with efficiency and produce high quality work.

Application deadline: 16th July 2025

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 employer: St Pancras Clinical Research

St Pancras Clinical Research is an exceptional employer, offering a vibrant work culture in the heart of London, where innovation meets compassion in clinical research. Employees benefit from a supportive environment that prioritises professional growth and development, alongside competitive salaries and a commitment to patient care. Join our dynamic team and contribute to meaningful advancements in healthcare while enjoying the unique advantages of working in a city renowned for its rich history and diverse opportunities.
S

Contact Detail:

St Pancras Clinical Research Recruiting Team

StudySmarter Expert Advice 🤫

We think this is how you could land Study Coordinator

✨Tip Number 1

Familiarise yourself with the latest ICH Good Clinical Practice (GCP) guidelines. Being well-versed in these regulations will not only boost your confidence but also demonstrate your commitment to maintaining high standards in clinical research.

✨Tip Number 2

Network with professionals in the clinical research field, especially those who have experience as Study Coordinators. Attend relevant conferences or webinars to gain insights and potentially make connections that could lead to job opportunities.

✨Tip Number 3

Prepare for potential interviews by practising common questions related to clinical trial management and patient care. Highlight your ability to work under pressure and manage multiple projects effectively, as these are key qualities sought by St Pancras Clinical Research.

✨Tip Number 4

Showcase your IT skills, particularly with Microsoft Office applications and electronic databases. Being proficient in these tools is essential for data management and will set you apart from other candidates.

We think you need these skills to ace Study Coordinator

Clinical Trial Management
Good Clinical Practice (GCP)
Patient Recruitment
Data Management
Attention to Detail
Administrative Skills
Laboratory Skills
IT Literacy
Microsoft Office Proficiency
Electronic Database Management
Time Management
Team Collaboration
Problem-Solving Skills
Ability to Work Under Pressure
Project Management

Some tips for your application 🫡

Understand the Role: Read the job description thoroughly to understand the responsibilities and requirements of the Study Coordinator position. Tailor your application to highlight relevant experience and skills that match what St Pancras Clinical Research is looking for.

Highlight Relevant Experience: Make sure to emphasise your clinical research coordinator experience, especially in CTIMPs. Provide specific examples of your past roles and how they relate to the responsibilities outlined in the job description.

Showcase Your Skills: Demonstrate your understanding of ICH Good Clinical Practice (GCP) and your patient-centric approach. Mention any IT skills, particularly with Microsoft Office applications and data entry systems, as these are crucial for the role.

Craft a Strong Cover Letter: Write a compelling cover letter that not only summarises your qualifications but also conveys your enthusiasm for the role and the company. Make it personal and specific to St Pancras Clinical Research to stand out from other applicants.

How to prepare for a job interview at St Pancras Clinical Research

✨Know Your Clinical Trials

Familiarise yourself with the specific clinical trials that St Pancras Clinical Research is currently conducting. Understanding the protocols and objectives of these trials will demonstrate your genuine interest and preparedness during the interview.

✨Highlight Your GCP Knowledge

Since a strong understanding of ICH Good Clinical Practice (GCP) is crucial for this role, be ready to discuss your experience with GCP guidelines. Prepare examples of how you've applied these principles in your previous roles.

✨Showcase Your Patient-Centric Approach

Emphasise your commitment to patient care and how you ensure a patient-centric approach in clinical research. Share specific instances where you prioritised patient welfare in your previous work.

✨Demonstrate Your Team Player Skills

As the role requires working closely with a clinical team, be prepared to discuss your experiences as a team player. Highlight situations where you collaborated effectively with others to achieve common goals, especially under pressure.

S
Similar positions in other companies
UK’s top job board for Gen Z
discover-jobs-cta
Discover now
>