Clinical Research Assistant

Position Overview

We are seeking a motivated and detail-oriented Clinical Research Assistant to join our growing clinical operations team. In this role, you will support the coordination and administration of clinical research studies while ensuring study documentation, data quality, and regulatory compliance are maintained throughout the research process.

This position is ideal for someone with excellent organizational skills, strong attention to detail, and an interest in contributing to clinical research in a remote environment. Essential Responsibilities Assist with the day-to-day management of assigned clinical studies. Maintain investigator site files, regulatory binders, and essential study documents.

Prepare, review, and file research documentation in accordance with study requirements. Support participant scheduling and study visit coordination. Enter, verify, and reconcile clinical data within electronic research systems. Monitor study timelines and assist with tracking project deliverables. Communicate effectively with investigators, sponsors, study participants, and internal research teams.

Identify and escalate documentation discrepancies or protocol deviations when appropriate. Ensure research activities are conducted in compliance with ICH Good Clinical Practice (GCP), study protocols, and applicable regulatory requirements. Perform additional administrative and research support duties as assigned.

Requirements

Qualifications Required Bachelor's degree in Life Sciences, Health Sciences, Nursing, Public Health, or a related discipline, or equivalent healthcare experience. Strong organizational and problem-solving abilities. Excellent verbal and written communication skills. High level of accuracy and attention to detail. Proficiency with Microsoft Office and web-based software applications.

Ability to manage multiple priorities while working independently in a remote setting. Preferred Previous experience supporting clinical research or healthcare operations. Familiarity with ICH-GCP guidelines and FDA regulations. Experience using Electronic Data Capture (EDC), CTMS, or eTMF systems. Knowledge of clinical trial documentation and research workflows.

Work Schedule Full-time Monday through Friday Standard business hours Benefits Benefits Competitive salary Comprehensive medical, dental, and vision coverage 401(k) with employer contribution Paid time off and company holidays Remote work environment Professional development and career advancement opportunities