Clinical Research Assistant

Benefits

Qualifications

• •This is an excellent entry-level opportunity for individuals looking to launch a career in clinical research
• •Bachelor's degree in life sciences, health sciences, nursing, or a related field (or equivalent experience)
• •Strong attention to detail and ability to follow complex protocols
• •Excellent organizational and time management skills
• •Proficiency with Microsoft Office Suite (Word, Excel, Outlook)
• •Strong verbal and written communication skills
• •3 more items(s)

Responsibilities

• •We are seeking a detail-oriented and motivated Research Assistant to join our growing clinical trials team
• •In this role, you will provide essential operational and administrative support across multiple clinical studies, working under the guidance of Clinical Research Coordinators and the site leadership team
• •Assist Clinical Research Coordinators with day-to-day study operations and participant management
• •Screen and schedule potential study participants; assist with informed consent processes
• •Collect, process, and accurately document study data in source documents and electronic data capture (EDC) systems
• •Perform study-related assessments including vital signs, ECGs, and specimen collection per protocol
• •Maintain regulatory binders and ensure documentation is current and audit-ready
• •Coordinate laboratory sample processing, labeling, and shipping according to study protocols
• •Assist with preparation for sponsor monitoring visits and audits
• •Maintain participant confidentiality and adhere to HIPAA guidelines at all times
• •Communicate professionally with study participants, sponsors, and internal team members
• •Contribute to a positive site culture and support continuous process improvement
• •Opportunity to contribute to meaningful medical research that impacts patient care
• •Collaborative and growth-oriented team culture
• •Expanding clinical network with strong operational leadership and support
• •12 more items(s)