University Intern – Clinical Trial Coordinator

Boehringer Ingelheim

. Provide administrative support to clinical trial teams at country and clinical trial site level .

Posted 10/14/2026internshipWinnersh • United KingdomEntry Level💰 £26,000 per yearWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates strong administrative and organizational skills to support clinical trial operations, ensuring compliance with ICH-GCP and Good Documentation Practices. Capable of effective communication and collaboration with stakeholders while managing multiple tasks and deadlines.

Highest-signal resume keywords

Administrative SupportRegulatory ComplianceClinical Trial OperationsMicrosoft Office ProficiencyTime Management

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Clinical Trial ManagementGood Documentation PracticeICH-GCP UnderstandingFeasibility AssessmentTrial Start-UpTrial MaintenanceTrial Reporting

Soft Skills

Organizational CapabilityClient-Oriented ThinkingClear CommunicationCollaborative ApproachAdaptability

Tools & Technologies

Technical Systems ManagementAI Utilization

Industry Keywords

Life Sciences DegreeDrug Development ProcessTrial Master File Management

About the role

Key responsibilities & impact

Provide administrative support to clinical trial teams at country and clinical trial site level
Plan, coordinate and carry out regulatory-defined tasks in line with ICH-GCP, Good Documentation Practice, SOPs and Working Instructions
Support smooth trial operations and 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
Gain experience across feasibility, trial start-up, maintenance, completion and reporting stages

Requirements

What you’ll need

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
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
Ability to manage multiple assignments while maintaining quality and meeting timelines
Understanding of the drug development process and the role of clinical trials is desirable
Client-oriented thinking when communicating with internal and external stakeholders is desirable
Clear and professional written and verbal communication
Collaborative approach and ability to build positive relationships
Ability to organise tasks, manage time and meet agreed deadlines
Ownership of learning, willingness to ask questions and respond positively to feedback
Adaptability to changing priorities, with curiosity and initiative
Appropriate use of AI
Confidence with Microsoft Office and willingness to learn new systems and technology
Professional conduct and adherence to relevant policies, procedures, legal obligations, and health, safety and environmental requirements

Benefits

Comp & perks

Meaningful work and real responsibilities from the start
Clear placement plan with key projects, milestones and learning goals
Support from manager, team and HR, with regular feedback and development conversations
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
Opportunity to build professional confidence, workplace skills and an organisational network
Training in clinical trial management systems and related platforms