Research Coordinator

Requirements

• Coordinate all aspects of research studies, including participant recruitment, scheduling, and data collection.
• Ensure strict adherence to research protocols, ethical standards, and regulatory requirements.
• Implement participant recruitment strategies, ensuring eligible individuals' enrollment in research studies.
• Facilitate the informed consent process, ensuring participants fully understand the study procedures, risks, and benefits.
• Oversee the collection, recording, and management of research data, maintaining accuracy and integrity.
• Collect biospecimens (e.g. blood, saliva, etc.), administer injections, and/or conduct rapid sexually transmitted infection testing with research participants.
• Collaborate with principal investigators, research staff, and external partners to facilitate smooth study operations.
• Monitor and track study progress, identifying and addressing any issues or deviations from the research protocol.
• Implement quality control measures to ensure the accuracy and completeness of research data.
• Prepare regular progress reports, contribute to manuscripts, and assist in the dissemination of research findings.
• Perform any and all other duties assigned by the supervisor.

Benefits

• Generous paid time off, including 12 paid holidays.
• 401k with 100% employer match up to 5%
• 12 weeks of fully paid parental leave
• Employer subsidized medical, dental, vision benefits
• Gender-affirming care benefits
• Employer paid short and long-term disability
• Tuition reimbursement
• Certification, and licensure assistance