Description

• Start your day by reviewing the study schedule, supplies, and priorities with the research team. 
• Support investigators by preparing for and executing assigned studies in line with protocol, SOPs, and GCP. 
• Recruit and screen potential participants, maintain screening logs, and help guide the consent process. 
• Coordinate and conduct study visits and procedures (vital signs, ECG, sample collection, spirometry, and other protocol-required tasks). 
• Collect, record, and maintain accurate source documentation and study data—quality and completeness matter. 
• Monitor participant safety and communicate adverse events/reactions to the Principal Investigator and appropriate medical staff. 
• Prepare for monitoring visits, audits, and inspections while protecting confidential information and PHI. 

• Bachelor’s degree in a related field. 
• 1–2 years of clinical research experience (or relevant clinical/medical experience with equivalent training). 
• Working knowledge of clinical trials, research documentation, and medical terminology. 
• Ability to apply GCP/ICH principles and applicable FDA regulations and guidelines for human subject protection. 
• Comfort performing clinical procedures as required (e.g., phlebotomy, vital signs; other procedures as assigned). 
• Strong written and verbal communication skills and the ability to build effective working relationships. 
• Excellent organization, attention to detail, and ability to multi-task and manage competing priorities. 
• Proficiency with Microsoft Office and routine office/clinical equipment. 

• You enjoy a fast-paced clinical environment and can stay calm and effective when priorities shift. 
• You take pride in data quality, documentation, and doing things the right way. 
• You’re a team player who communicates clearly and likes solving problems alongside others.