University Intern - Clinical Trial Coordinator

INTRODUCING THE OPPORTUNITY

WHAT YOU WILL DO

• Plan, coordinate and carry out regulatory-defined tasks in line with internal and external standards, including ICH-GCP, Good Documentation Practice, SOPs and Working Instructions.
• Support smooth trial operations and clear communication with relevant 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.
• You will gain experience across different stages of a clinical trial, including feasibility, trial start-up, maintenance, completion and reporting. You will develop an understanding of the local clinical research environment, regulations and clinical trial site operations, while building transferable skills through collaboration with cross-functional teams and external stakeholders. You will also receive training in clinical trial management systems and other related platforms.
• Meaningful work and real responsibilities from the start, with opportunities to contribute to projects that matter.
• Joining with a large cohort of exceptional students, you will receive a clear placement plan setting out key projects, milestones and your learning goals for the year.
• Support from your manager, your team and HR, with regular feedback and development conversations.
• Learning opportunities beyond the role, including workshops, networking, career insights and exposure to different parts of the business.
• Access to coaching, mentoring and online learning resources, including Boehringer’s virtual University.
• The opportunity to build professional confidence, workplace skills and a network across the organisation.
• Currently studying for a Life Sciences degree and completing a placement year as part of the course.
• A minimum of three A levels at grades BBC, with at least one grade in a science subject, or equivalent.
• The right to work in the UK for the full duration of the internship.
• The 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.
• An understanding of the drug development process and the role of clinical trials.
• Client-oriented thinking when communicating with internal and external stakeholders.

WHAT YOU WILL GAIN

WHAT YOU CAN EXPECT FROM A BOEHRINGER INGELHEIM INTERNSHIP

ESSENTIAL REQUIREMENTS

DESIRABLE REQUIREMENTS

SKILLS AND BEHAVIOURS

WHY THIS IS A GREAT PLACE TO WORK

Qualifications

• AND BEHAVIOURS
• Communicates clearly and professionally in writing and conversation.
• Works collaboratively, builds positive relationships and contributes own ideas proactively.
• Organises tasks, manages time and meets agreed deadlines.
• Takes ownership of learning, asks questions and responds positively to feedback.
• Adapts to changing priorities and approaches work with curiosity and initiative.
• Uses AI appropriately to deliver work. Confident with Microsoft Office and is willing to learn new systems and technology.
• Acts professionally and follows relevant policies, procedures, legal obligations and health, safety and environmental requirements.
• WHY THIS IS A GREAT PLACE TO WORK
• Boehringer Ingelheim has been recognised as a Top Employer in the UK. Being certified as a Top Employer confirms our dedication to a better world of work, delivered through excellent HR policies and people practices. To learn more visit: https://www.boehringer-ingelheim.co.uk/careers/uk-careers/why-great-place-work
• Currently studying for a Life Sciences degree and completing a placement year as part of the course.
• A minimum of three A levels at grades BBC, with at least one grade in a science subject, or equivalent.
• The right to work in the UK for the full duration of the internship.
• The 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.
• DESIRABLE REQUIREMENTS
• An understanding of the drug development process and the role of clinical trials.
• Client-oriented thinking when communicating with internal and external stakeholders.
• SKILLS AND BEHAVIOURS