Study Coordinator

Study Coordinator

London Entry level 30000 - 42000 £ / year (est.) No home office possible
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TFS HealthScience

At a Glance

  • Tasks: Coordinate clinical trials, manage data entry, and support site operations.
  • Company: Join TFS HealthScience, a global leader in clinical research.
  • Benefits: Competitive pay, benefits, and a chance to work on impactful studies.
  • Why this job: Make a difference in healthcare while collaborating with international teams.
  • Qualifications: Experience in clinical research and strong organisational skills required.
  • Other info: Dynamic role with opportunities for growth in a supportive environment.

The predicted salary is between 30000 - 42000 £ per year.

TFS HealthScience is a leading global mid-size Contract Research Organization (CRO) partnering with biotechnology and pharmaceutical companies throughout their entire clinical development journey. Our expertise spans full-service solutions, resourcing, and Functional Service Provider (FSP) models.

About This Role

As part of our SRS/FSP team, you will be dedicated to one of our pharmaceutical partners, supporting the conduct of hospital-based clinical trials in the UK. The Study Coordinator will play a key role in ensuring accurate data entry, query resolution, and smooth site operations across study locations in London, Cambridge, and Cardiff. This role focuses on oncology and infectious diseases.

Responsibilities

  • Perform accurate and timely data entry into study systems.
  • Manage and resolve data queries in collaboration with site staff and CRAs.
  • Support day-to-day study operations, including scheduling patient visits and maintaining documentation.
  • Ensure compliance with study protocols, GCP, and site SOPs.
  • Act as a liaison between site staff, sponsor, and CRO teams.
  • Assist with monitoring visits, audits, and site readiness activities.

Qualifications

Required:

  • Previous experience as a Study Coordinator, Research Nurse, or Clinical Research Professional.
  • Strong background in hospital-based clinical studies.
  • Knowledge of GCP and clinical trial regulations.
  • Excellent organizational and communication skills, with strong attention to detail.
  • Ability to work independently while collaborating effectively with cross-functional teams.

Nice To Have:

  • Experience in oncology and/or infectious disease studies.
  • Familiarity with electronic data capture (EDC) systems.

What We Offer

  • Competitive compensation and benefits.
  • Opportunity to work on impactful studies in a collaborative international environment.

About TFS

Our journey began more than 25 years ago in Lund, Sweden. Today, TFS operates in 17 countries across Europe, North America, Asia-Pacific, and the Middle East, delivering tailored clinical development solutions to our partners. Our core values — Trust, Quality, Flexibility, and Passion — define who we are and guide how we work. They are the foundation of our culture and our success.

Seniority level

  • Entry level

Employment type

  • Full-time

Job function

  • Research, Analyst, and Information Technology

Industries

  • Pharmaceutical Manufacturing

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Study Coordinator employer: TFS HealthScience

TFS HealthScience is an exceptional employer, offering a dynamic work environment where you can contribute to meaningful clinical trials in oncology and infectious diseases. With a strong emphasis on collaboration and professional growth, employees benefit from competitive compensation, comprehensive training, and the opportunity to work alongside leading experts in the field across key UK locations like London, Cambridge, and Cardiff. Our core values of Trust, Quality, Flexibility, and Passion foster a supportive culture that empowers you to excel in your role as a Study Coordinator.
TFS HealthScience

Contact Detail:

TFS HealthScience Recruiting Team

StudySmarter Expert Advice 🤫

We think this is how you could land Study Coordinator

✨Tip Number 1

Network like a pro! Reach out to your connections in the clinical research field, especially those who have worked with TFS HealthScience. A friendly chat can lead to insider info about job openings and even referrals.

✨Tip Number 2

Prepare for interviews by brushing up on your knowledge of GCP and clinical trial regulations. We want you to shine when discussing your experience as a Study Coordinator or in similar roles. Practice common interview questions to boost your confidence!

✨Tip Number 3

Showcase your organisational skills! During interviews, share specific examples of how you've managed data entry and resolved queries in past roles. This will demonstrate your attention to detail and ability to handle study operations smoothly.

✨Tip Number 4

Don't forget to apply through our website! It’s the best way to ensure your application gets noticed. Plus, it shows you're genuinely interested in joining our team at TFS HealthScience.

We think you need these skills to ace Study Coordinator

Data Entry
Query Resolution
Study Operations Management
Compliance with GCP
Knowledge of Clinical Trial Regulations
Organisational Skills
Communication Skills
Attention to Detail
Independent Working
Collaboration with Cross-Functional Teams
Experience in Oncology Studies
Experience in Infectious Disease Studies
Familiarity with Electronic Data Capture (EDC) Systems

Some tips for your application 🫡

Tailor Your CV: Make sure your CV is tailored to the Study Coordinator role. Highlight your experience in clinical studies, especially in oncology or infectious diseases, and showcase your organisational skills. We want to see how your background aligns with what we do!

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 you can contribute to our team. Be sure to mention any relevant experience and your understanding of GCP and clinical trial regulations.

Showcase Your Attention to Detail: As a Study Coordinator, attention to detail is key. In your application, provide examples of how you've successfully managed data entry and resolved queries in past roles. This will demonstrate that you’re the right fit for ensuring compliance and smooth operations.

Apply Through Our Website: We encourage you to apply through our website for the best chance of getting noticed. It’s straightforward and ensures your application goes directly to us. Plus, you’ll find all the info you need about the role and our company culture there!

How to prepare for a job interview at TFS HealthScience

✨Know Your Stuff

Make sure you brush up on your knowledge of GCP and clinical trial regulations. Familiarise yourself with the specifics of oncology and infectious diseases, as this will show your potential employer that you're genuinely interested in the role and understand the field.

✨Showcase Your Experience

Prepare to discuss your previous experience as a Study Coordinator or in similar roles. Be ready to share specific examples of how you've managed data entry, resolved queries, and supported study operations. This will help demonstrate your capability and fit for the position.

✨Communication is Key

Since the role involves liaising between various teams, practice articulating your thoughts clearly. Think about how you can convey complex information simply and effectively, as strong communication skills are essential for this job.

✨Ask Smart Questions

Prepare thoughtful questions about the company culture, team dynamics, and the specific studies you'll be involved in. This not only shows your enthusiasm but also helps you gauge if the company aligns with your values and career goals.

Study Coordinator
TFS HealthScience
Location: London
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