Vaccine Trial Assistant Coordinator

Profound Research LLC; New York (NY); On-site; USD 34,000 - 55,000; Full time

Job summary

Profound Research LLC in New York is seeking an Assistant Clinical Research Coordinator to support high-volume vaccine trials. You will learn study coordination, patient interaction, data collection, and clinical procedures in a fast-paced, site-based environment.

This 1099 independent contractor role offers on-site work, with potential to convert to full-time depending on business needs and performance. You’ll work with experienced staff and leaders to ensure compliant, patient-centered trial

Qualifications

• High school diploma or technical degree with 3+ years of relevant experience in life sciences
• Associate’s degree with 1+ year of relevant experience in a clinical or life sciences setting
• Bachelor’s degree with relevant coursework or experience in a clinical or life sciences setting
• Ability to maintain confidentiality and follow structured processes
• Comfortable working in a fast-paced, team-based environment

Responsibilities

• Support coordination of high-volume vaccine trials, including patient visits and study-related procedures
• Assist with data collection and documentation while applying Good Clinical Practice standards
• Perform and develop competency in clinical procedures such as vital signs, EKGs, phlebotomy, and specimen processing
• Help prepare for and support efficient participant visits, including rooming patients and organizing supplies
• Communicate clearly with study participants and site team about patient needs and visit flow
• Work closely with Clinical Research Coordinators and site leadership to build clinical knowledge
• Follow study protocols, SOPs, and infection control expectations for compliant trial execution
• Maintain organized study materials, supplies, and lab-related workflows

Job description

Profound Research LLC in New York is seeking an Assistant Clinical Research Coordinator to support high-volume vaccine trials. You will learn study coordination, patient interaction, data collection, and clinical procedures in a fast-paced, site-based environment.

This 1099 independent contractor role offers on-site work, with potential to convert to full-time depending on business needs and performance. You’ll work with experienced staff and leaders to ensure compliant, patient-centered trial