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University Intern – Clinical Trial Feasibility Coordinator
Boehringer Ingelheim. Support the UK and Ireland team in assessing whether sites and investigators are suitable for upcoming clinical trials .
Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates strong analytical skills in gathering and interpreting trial metric data, with a solid understanding of the drug development process and clinical trials. Proficient in using digital tools for feasibility assessments and maintaining organized trackers and dashboards.
Highest-signal resume keywords
Data AnalysisClinical Trial KnowledgeMicrosoft Office ProficiencyProject CoordinationCommunication Skills
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills
Data ReportingFeasibility AssessmentTrial Metric InterpretationRegulatory KnowledgeSite Operations Understanding
Soft Skills
CollaborationTime ManagementAdaptabilityCuriosityInitiative
Tools & Technologies
Digital ToolsSecure Data Environments
Industry Keywords
Clinical ResearchDrug DevelopmentFeasibility ActivitiesInvestigator MeetingsExpressions of Interest
About the role
Key responsibilities & impact- Support the UK and Ireland team in assessing whether sites and investigators are suitable for upcoming clinical trials
- Use digital tools and secure data environments for country- and site-level feasibility assessments
- Maintain trackers and dashboards for feasibility activities
- Gather, analyse and present information from multiple sources
- Prepare materials for investigator or feasibility meetings
- Distribute, collect and organise expressions of interest and site feasibility questionnaires
- Provide practical insights to support trial placement decisions
- Develop knowledge of local clinical research environments, regulations and site operations
- Collaborate with cross-functional teams and develop practical skills in data reporting, analysis and project coordination
Requirements
What you’ll need- Currently studying for a Life Sciences degree and completing a placement year as part of the course
- Minimum of three A levels at grades ABB, or equivalent; at least one grade must be in a science subject
- 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
- Ability to gather, review and interpret trial metric data, identify patterns and gaps, and summarise data for feasibility decisions
- Understanding of the drug development process and the role of clinical trials 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 deadlines
- Willingness to learn, ask questions and respond positively to feedback
- Adaptability, 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
- Regular feedback and development conversations
- Workshops, networking, career insights and exposure to different parts of the business
- Coaching, mentoring and online learning resources, including Boehringer’s virtual University
- Opportunity to build professional confidence, workplace skills and an organisation-wide network
- Paid 12-month internship