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Clinical Operations Intern
Infotree Global Solutions. Support Clinical Trial Management Associates (CTMAs) and Clinical Research Associates (CRAs) in keeping trial operations running smoothly .
Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates proficiency in managing clinical trial documentation and compliance with regulatory standards while maintaining operational efficiency. Strong organizational skills and attention to detail are essential for supporting Clinical Trial Management Associates and Clinical Research Associates.
Highest-signal resume keywords
Clinical Trial Documentation ManagementRegulatory ComplianceMS Office ProficiencyOrganizational SkillsAttention to Detail
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills
Trial Master File ActivitiesData Entry and MaintenanceOperational ReportingQuality VerificationTrial Documentation Tracking
Soft Skills
Clear Communication SkillsProactive AttitudeExcellent Organizational Abilities
Tools & Technologies
MS OfficeExcelPowerPointCanvaAI Tools
Industry Keywords
Clinical Trial ManagementLife SciencesPharmacyBiotechnologyChemistry
About the role
Key responsibilities & impact- Support Clinical Trial Management Associates (CTMAs) and Clinical Research Associates (CRAs) in keeping trial operations running smoothly
- Track trial documentation
- Conduct Trial Master File (TMF) activities, including uploading, indexing, and quality verification
- Ensure compliance with regulatory standards
- Enter and maintain critical trial data across internal systems
- Maintain operational trackers
- Prepare operational reports and presentation materials for clinical trial updates
- Assist CRAs/monitors with daily administrative and operational duties
Requirements
What you’ll need- Active student status required
- Preferably pursuing a degree in Pharmacy, Biotechnology, Chemistry, Physics, or a related Life Sciences field
- Proficiency in MS Office, including Excel and PowerPoint
- Familiarity with graphic design tools such as Canva
- Practical understanding of AI tools
- Good command of English, minimum B2 level
- Excellent organizational abilities
- Strong attention to detail
- Proactive attitude
- Clear communication skills
Benefits
Comp & perks- Gain practical, real-world experience in the clinical research industry
- Mentorship from seasoned industry professionals
- Flexible working environment tailored around your university schedule
- 100% remote work
- 25 hours per week, Monday–Friday between 8AM–5PM