CRO-Clinical Monitoring Support Associate

Company Overview

Evolution Research Group’s Lotus Clinical Research division stands apart through its shared ownership structure, which connects it closely with ERG. Its US-based network includes 20 fully owned research units, more than 400 beds, nine surgical centers, and several Phase 1 units. This setup supports both healthy volunteer studies and focused patient research in areas such as neuroscience and metabolic disease.

The Lotus-ERG model helps studies begin faster because many time-consuming startup steps, such as contracting and legal work, are already established. Teams in leadership, medical, and operations stay in close contact, and Lotus-sponsored studies are given priority.

Employees can expect a collaborative workplace, meaningful responsibilities, and the chance to work with experienced professionals on advanced research. The benefits package includes medical and dental coverage, a matching 401(k), and paid time off.

Role Summary

The CRO-Clinical Monitoring Support Associate supports clinical trial operations from a remote setting and helps protect the accuracy, completeness, and compliance of study data. The role works closely with clinical monitors, project managers, and other internal or external partners to keep trials moving smoothly and in line with regulatory expectations. It includes organizing trial records, following study milestones, and helping address data-related issues. Through timely and careful support, the associate contributes to efficient, ethical clinical research across the United States healthcare environment.

What You Will Do

• Help clinical monitors prepare, update, and maintain core study documents and regulatory binders.
• Monitor study progress, including enrollment levels, data entry status, and site compliance, and share updates as needed.
• Assist with resolving data queries by coordinating between clinical sites and data management teams.
• Keep communication flowing among trial sites, monitors, and internal stakeholders so information is delivered on time.
• Record monitoring visits, follow-up tasks, and study correspondence accurately while following SOPs and regulatory rules.

Required Qualifications

• A bachelor’s degree in life sciences, health sciences, or a closely related discipline.
• Working knowledge of clinical research processes and Good Clinical Practice (GCP) principles.
• Comfort using Microsoft Office applications, including Word, Excel, and PowerPoint, along with clinical trial management systems.
• Strong planning and organizational ability, with the capacity to handle several tasks at once.
• Clear written and spoken English communication skills.

Preferred Qualifications

• Prior experience in a clinical research organization or healthcare environment.
• Exposure to electronic data capture (EDC) tools and clinical trial management software.
• Clinical research certification such as CCRC or CCRA, or a similar credential.
• Understanding of US-specific clinical trial regulatory requirements.
• Ability to work well in a team and adjust to shifting project priorities.

Benefits

• Medical coverage
• Dental coverage
• Matching 401(k)
• Paid time off

Additional Information

This position supports clinical research activities conducted within the United States. The role is remote and intended for full-time employment.