CRO, Clinical Monitoring Support Associate

Evolution Research Group

CRO-Clinical Monitoring Support Associate supporting clinical trial operations ensuring accuracy and compliance of clinical data. Collaborating with teams to organize clinical trial documentation and track study progress.

Posted 6/12/2026full-timeRemote • 🇺🇸 United StatesJuniorMid-LevelWebsite

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

clinical research processesGood Clinical Practice (GCP)clinical trial management systemsdata managementdata integritydata accuracyregulatory compliance

Soft Skills

organizational skillsattention to detailmultitaskingwritten communicationverbal communication

Tools & Technologies

Microsoft Office SuiteWordExcelPowerPoint

Industry Keywords

clinical trial operationsclinical datastakeholder collaboration

Tech Stack

Tools & technologies

Google Cloud Platform

About the role

Key responsibilities & impact

Supporting clinical trial operations to ensure the integrity, accuracy, and compliance of clinical data collected during studies.
Collaborating closely with clinical monitors, project managers, and other stakeholders to facilitate smooth trial execution and adherence to regulatory standards.
Managing and organizing clinical trial documentation, tracking study progress, and assisting in the resolution of data queries.
Maintaining high-quality data and supporting the overall success of clinical research projects.

Requirements

What you’ll need

Bachelor’s degree in life sciences, health sciences, or a related field.
Basic understanding of clinical research processes and Good Clinical Practice (GCP) guidelines.
Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint) and clinical trial management systems.
Strong organizational skills with attention to detail and ability to manage multiple tasks simultaneously.
Excellent written and verbal communication skills in English.

Benefits

Comp & perks

medical and dental coverage
matching 401(k)
paid time off