Clinical Research Intern

CPC

. Prepare slides with academic activities for monthly staff meeting presentations .

Posted 10/1/2026internshipAurora • Colorado • United StatesEntry Level💰 $20 per hourWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates proficiency in preparing presentations and managing documentation for clinical trials, with strong organizational and communication skills. Familiarity with Clinical Trial Management Systems and regulatory submission processes is essential.

Highest-signal resume keywords

Clinical Trial Management System FunctionalityRegulatory SubmissionsMS Word ProficiencyMS PowerPoint ProficiencyMS Excel Proficiency

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Trial Master File SubmissionsQuality ChecksInstitutional Review Board SubmissionsBudget FunctionalityMeeting Minutes Taking

Soft Skills

Good Communication SkillsOrganizational SkillsAttention to DetailCritical Thinking Skills

Tools & Technologies

Clinicaltrials.govPubMed

Industry Keywords

Clinical TrialsScientific Field DegreeSite Regulatory DocumentationLunch & LearnsClinical Trial Operations

About the role

Key responsibilities & impact

Prepare slides with academic activities for monthly staff meeting presentations
Assist with monthly scientific Lunch & Learns, including speaker selection, slide preparation, meal ordering, conference room setup, and cleanup
Attend clinical trial operations calls and take meeting minutes
Participate in clinic shadowing opportunities with physician faculty
Complete Trial Master File submissions and quality checks while learning TMF functions
Assist with regulatory submissions and public trial registries for sponsored trials
Assist with site regulatory documentation collection during study site start-up shadowing
Learn Clinical Trial Management System functionality
Complete Institutional Review Board submissions
Learn budget functionality and role with the finance team
Attend Site Endpoint Evaluation Visits and functional endpoint remote trainings
Observe medical monitoring, narrative writing/shell building, DSMB, adjudication, and committee management activities
Use clinicaltrials.gov and PubMed

Requirements

What you’ll need

Enrollment in undergraduate or graduate scientific field degree program
Ability to attend in-person training
Good communication and organizational skills
Great attention to detail and critical thinking skills
Proficiency with MS Word, PowerPoint, and Excel
Ability to attend occasional office visits
Successful completion of background and education verification check

Benefits

Comp & perks

Flexible hours: 10–40 hours per week, adjustable to school schedule
In-person training opportunities
Professional learning opportunity and exposure to clinical research management
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