Student Placement - Clinical Research

Caraway Therapeutics, Inc.

Greater London

On-site

GBP 18,000 - 24,000

Full time

6 days ago
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Job summary

Caraway Therapeutics, Inc. in London is offering a 12-month Clinical Research Student Placement to gain hands-on experience in coordinating clinical trials, study management, regulatory processes, and site-facing activities within the UK.

You will work as a trainee Clinical Trial Co-Ordinator, with supervision for field visits and practical training in trial systems and processes. The role is based in Moorgate, London, in modern co-working facilities, providing exposure to global clinical

Qualifications

  • You must be currently studying at a UK university and will be looking to complete a 12-month student internship as part of your undergraduate degree.
  • Studying towards a degree in Biomedical Sciences, Pharmaceutical Sciences or a related life sciences discipline.
  • Working knowledge of Microsoft Office packages (e.g. Word, Excel, PowerPoint)
  • Demonstrates an appreciation of current topics in clinical research and clinical trial conduct

Responsibilities

  • Support study teams in the day-to-day coordination and delivery of clinical trials across a range of activities.
  • Assist with the preparation, maintenance, and management of study documentation to support regulatory and ethics submissions.
  • Support budgeting and financial tracking activities throughout the clinical trial lifecycle.
  • Gain exposure to clinical trial sites by participating in on-site monitoring activities alongside experienced clinical research professionals.
  • Contribute to departmental initiatives, meetings, and events while building knowledge of clinical research processes and best practices.
  • Develop an understanding of clinical trial systems, regulations, and operational activities through structured training and practical experience.

Skills

Clinical Research
Data Analytics
CTMS
Regulatory Knowledge
Trial Monitoring
Office Applications
Data Entry
Documentation

Education

Biomedical Sciences degree
Pharmaceutical Sciences degree
Life sciences degree

Tools

Microsoft Office

Job description

Job Description

12-Month Clinical Research Student Placement offering hands-on experience in clinical trial coordination, study management, regulatory processes, and site-facing clinical research activities.

As part of the Clinical Research team, you will work as trainee Clinical Trial Co-Ordinator. Providing office-based support to the teams that work on our company clinical programs in the UK. The opportunity to conduct field visits at trial sites based in the UK under supervision Throughout your twelve months here, you will be given the opportunity to gain a full insight into the principles and practices of a Clinical Research Department within a global company. Working in a professional and friendly environment, you will support the members of our study teams, whilst developing your knowledge and practical skills in setting up and conducting clinical trials. Experiences will include field visits to our trial sites and training on our clinical management systems and processes.

This role will be based in our modern state-of-the-art co-working facilities in Moorgate, London . This site, at the heart of London provides fantastic amenities, support services and collaborative workspaces with convenient transport links.

We are a global biopharmaceutical leader committed to enhancing the lives of individuals through a diverse portfolio of prescription medicines, oncology treatments, life-saving vaccines, and animal health products. Our unwavering dedication to delivering innovative solutions is the driving force behind everything we do.

Responsibilities:
  • Support study teams in the day-to-day coordination and delivery of clinical trials across a range of activities.
  • Assist with the preparation, maintenance, and management of study documentation to support regulatory and ethics submissions.
  • Support budgeting and financial tracking activities throughout the clinical trial lifecycle.
  • Gain exposure to clinical trial sites by participating in on-site monitoring activities alongside experienced clinical research professionals.
  • Contribute to departmental initiatives, meetings, and events while building knowledge of clinical research processes and best practices.
  • Develop an understanding of clinical trial systems, regulations, and operational activities through structured training and practical experience.
Requirements:
  • You must be currently studying at a UK university and will be looking to complete a 12-month student internship as part of your undergraduate degree.
  • Studying towards a degree in Biomedical Sciences, Pharmaceutical Sciences or a related life sciences discipline.
  • Working knowledge of Microsoft Office packages (e.g. Word, Excel, PowerPoint)
  • Demonstrates an appreciation of current topics in clinical research and clinical trial conduct
Equal Opportunity Employer:

We are proud to be a company that embraces the value of bringing diverse, talented, and committed people together. The fastest way to breakthrough innovation is when diverse ideas come together in an inclusive environment. We encourage our colleagues to respectfully challenge one another’s thinking and approach problems collectively. We are an equal opportunity employer, committed to fostering an inclusive and diverse workplace.

For more Information visit our Future Talent page!

#UKFT26

Required Skills:
  • Analytical Problem Solving
  • Analytical Problem Solving
  • Biomedical Research
  • Clinical Data Interpretation
  • Clinical Reporting
  • Clinical Research
  • Clinical Research Operations
  • Clinical Trial Development
  • Clinical Trial Management
  • Clinical Trial Management Systems (CTMS)
  • Clinical Trials Monitoring
  • Data Analytics
  • Database Management
  • Data Entry
  • Data Visualization
  • Document Management
  • Health Economics
  • Life Science
  • Observational Studies
  • Office Applications
  • Patient Support
  • Patient Support Programs
  • Process Improvements
  • Project Management
  • Regulatory Documents {+ 7 more}
Employee Status:

Intern/Co-op (Fixed Term)

Relocation:

No relocation

VISA Sponsorship:

No

Travel Requirements:

No Travel Required

Flexible Work Arrangements:

Not Applicable

Shift:

Not Indicated

Valid Driving License:

No

Hazardous Material(s):

no

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