Clinical Trial Study Coordinator in Glasgow

Clinical Trial Study Coordinator in Glasgow

Glasgow Full-Time 36000 - 60000 € / year (est.) No home office possible
Planet Pharma

At a Glance

  • Tasks: Coordinate clinical trials, manage patient records, and support research staff.
  • Company: Join Planet Pharma, a leading global staffing agency in clinical research.
  • Benefits: Permanent position with opportunities for career growth and professional development.
  • Other info: Dynamic work environment with a focus on diversity and inclusion.
  • Why this job: Make a difference in healthcare by supporting innovative clinical studies.
  • Qualifications: Experience in healthcare settings and strong organisational skills required.

The predicted salary is between 36000 - 60000 € per year.

Position: Clinical Trial Administrator/Clinical Study Coordinator

Location: Bedford, UK - On-site

Client: UK Clinical Research Company

Type: Permanent

Main Responsibilities

  • Act as first point of contact for the clinical research unit, providing front-of-house support and ensuring smooth daily operations.
  • Chase, collect and organise patient medical records, liaise with GP practices and physicians, and ensure all documentation is complete and compliant.
  • Coordinate and schedule patient visits, maintaining accurate records and supporting participants throughout the study process.
  • Provide administrative support across the site, including managing study files, tracking documentation, and assisting with regulatory or sponsor-related queries.
  • Support clinical staff, research nurses, and study sponsors to ensure studies run efficiently and according to protocols.

Main Requirements

  • Experience in a clinical research site, GP surgery, hospital clinic, or similar healthcare setting (e.g., Coordinator, Administrator, Clinic Support, Medical Secretary, or Band 4 equivalent).
  • Strong organisational skills with the ability to chase information, manage records, prioritise tasks, and coordinate patient appointments.
  • Confident communicator able to liaise professionally with GPs, physicians, patients, and external study sponsors.
  • Administrative accuracy and attention to detail, with experience maintaining sensitive medical information.

Clinical Trial Study Coordinator in Glasgow employer: Planet Pharma

At Planet Pharma, we pride ourselves on being an exceptional employer, offering a supportive and dynamic work environment in Bedford, UK. Our commitment to employee growth is evident through our extensive training programmes and opportunities for career advancement within the clinical research field. With a strong focus on collaboration and excellence, we ensure that our team members are equipped with the resources they need to thrive while making a meaningful impact in the healthcare sector.

Planet Pharma

Contact Detail:

Planet Pharma Recruiting Team

StudySmarter Expert Advice🤫

We think this is how you could land Clinical Trial Study Coordinator in Glasgow

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 refer you directly.

Tip Number 2

Prepare for interviews by researching the company and understanding their studies. Be ready to discuss how your experience aligns with their needs. Practise common interview questions and think of examples that showcase your organisational skills and attention to detail.

Tip Number 3

Follow up after interviews! A quick thank-you email can go a long way in showing your enthusiasm for the role. It also keeps you fresh in the interviewer's mind, which is always a bonus.

Tip Number 4

Don’t forget to apply through our website! We’ve got loads of opportunities waiting for you, and applying directly can sometimes give you an edge. Plus, it’s super easy to keep track of your applications!

We think you need these skills to ace Clinical Trial Study Coordinator in Glasgow

Clinical Research Experience
Organisational Skills
Communication Skills
Administrative Accuracy
Attention to Detail
Patient Coordination
Record Management

Some tips for your application 🫡

Show Off Your Experience:Make sure to highlight any relevant experience you have in clinical research or healthcare settings. We want to see how your background aligns with the role of Clinical Trial Study Coordinator, so don’t hold back!

Be Organised:Since this role requires strong organisational skills, demonstrate your ability to manage records and coordinate tasks in your application. A well-structured CV and cover letter can really make a difference!

Communicate Clearly:As a confident communicator, it’s important to showcase your ability to liaise with various stakeholders. Use clear and professional language in your written application to reflect this skill.

Apply Through Our Website:We encourage you to apply directly through our website for the best chance of success. It’s the easiest way for us to receive your application and get to know you better!

How to prepare for a job interview at Planet Pharma

Know Your Stuff

Make sure you understand the ins and outs of clinical trials and the specific responsibilities of a Clinical Trial Study Coordinator. Brush up on relevant regulations and protocols, as well as the types of documentation you'll be handling. This will show your potential employer that you're not just interested in the role, but that you’re genuinely knowledgeable about it.

Show Off Your Organisational Skills

Since this role requires strong organisational abilities, prepare examples from your past experiences where you successfully managed records or coordinated appointments. Be ready to discuss how you prioritise tasks and ensure everything runs smoothly, as this will demonstrate your fit for the position.

Communicate Like a Pro

As a Clinical Trial Study Coordinator, you'll need to liaise with various stakeholders. Practice articulating your thoughts clearly and confidently. Consider role-playing with a friend to simulate potential interview questions, especially those related to communication with GPs, patients, and sponsors.

Attention to Detail is Key

Highlight your experience with maintaining sensitive medical information and ensuring accuracy in documentation. Prepare to discuss specific instances where your attention to detail made a difference in your previous roles. This will reassure the interviewer that you can handle the meticulous nature of clinical research.