Clinical Trial Coordinator Intern — Winnersh-based

Boehringer Ingelheim; Bracknell; On-site; GBP 18,000 - 24,000; Full time

Job summary

Boehringer Ingelheim in Winnersh, UK, offers a 12-month paid internship starting September 2027 in Clinical Trial Coordination. The role is office-based with at least two days per week on site and supports regulatory tasks, trial documentation and cross-functional collaboration for UK & Ireland trials.

You will gain experience across the clinical trial lifecycle, learn ICH-GCP standards and become proficient with trial systems, while receiving mentoring, a placement plan and opportunities to

Qualifications

• Minimum of three A levels at grades BBC, with at least one grade in a science subject.
• The right to work in the UK for the full duration of the internship.
• Ability to travel independently to the usual place of work and, where required, to other sites.
• Excellent administrative skills and strong organisational capability, with the ability to manage multiple assignments while maintaining quality and meeting timelines.

Responsibilities

• Plan, coordinate and carry out regulatory-defined tasks in line with internal and external standards (ICH-GCP, SOPs).
• Support smooth trial operations and clear communication with internal and external stakeholders.
• Work with clinical trial team members and investigator sites to support trial delivery in the UK and Ireland.
• Maintain and oversee technical systems used to manage clinical trials.
• Help ensure the Trial Master File is complete, accurate and high quality.

Skills

Clear communication

Time management

Organisational skills

Learning mindset

Proactive

AI usage

Microsoft Office

Education

Life Sciences degree (in progress)

A-levels (BBC) + science subject

Tools

Microsoft Office

Job description

Boehringer Ingelheim in Winnersh, UK, offers a 12-month paid internship starting September 2027 in Clinical Trial Coordination. The role is office-based with at least two days per week on site and supports regulatory tasks, trial documentation and cross-functional collaboration for UK & Ireland trials.

You will gain experience across the clinical trial lifecycle, learn ICH-GCP standards and become proficient with trial systems, while receiving mentoring, a placement plan and opportunities to