Assistant Clinical Research Coordinator

Assistant Clinical Research Coordinator

Responsibilities:
Assist with the preparation and submission of Institutional Review Board (IRB) protocols, amendments, continuing reviews, and related regulatory documents.
Assist with the administration and distribution of study questionnaires and surveys, including demographic, health-related quality of life, health mindset, and disease-specific assessments.
Assist with participant screening, recruitment, informed consent processes, enrollment, and study retention activities.
Enter and maintain study data in research databases, ensuring accuracy and completeness.
Assist with preparing and maintaining study-related documentation, including protocol worksheets, procedure manuals, regulatory binders, case report forms, and study reports.
Support data collection and management activities in accordance with study protocols and regulatory requirements.
Assist with scheduling participant visits and coordinating study procedures with clinical and research staff.
Maintain research records and ensure compliance with institutional, sponsor, and regulatory guidelines.
Perform other research-related duties as assigned.

Top 3 requirements to hire
Excellent organization and attention to detail, Strong communication/customer service skills, Demonstrated interest or experience in clinical research, healthcare, or science

Required experience:
1-2 years

Notes:
Onsite
Number of hours per week: 20

VIVA is an equal opportunity employer. All qualified applicants have an equal opportunity for placement, and all employees have an equal opportunity to develop on the job. This means that VIVA will not discriminate against any employee or qualified applicant on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.