Overview
We are seeking a dedicated and detail-oriented Clinical Research Coordinator to join our dynamic research team. In this vital role, you will participate in the operations of clinical trials, ensuring compliance with regulatory standards and maintaining high-quality data collection. Your approach will facilitate smooth study progress, support patient safety, and uphold the integrity of clinical research activities. This position offers an exciting opportunity to contribute to groundbreaking medical advancements while working in a collaborative and innovative environment.

Duties:

Coordinate and manage all aspects of clinical trials, including participant recruitment, scheduling, and follow-up visits
Ensure adherence to FDA regulations, ICH GCP guidelines, and institutional policies throughout the study lifecycle
Review and verify study documentation for accuracy, completeness, and compliance with protocol requirements
Monitor patient progress by collecting vital signs, blood samples through phlebotomy, and tracking adverse events
Conduct data collection and entry, using statistical software to support study outcomes

What we're looking for:

Outstanding interpersonal skills
Strong written, organizational, and problem-solving skills.
Experience in capturing patient medical history and medication
Experience with taking vitals
Prior experience in research environment is preferred, or equivalent combination of education and experience in a health-related field is a plus
Bachelor's degree required

Join us to be part of a team committed to advancing healthcare through meticulous research practices. Your expertise will directly impact the development of innovative treatments while fostering a culture of excellence in clinical research.

Benefits:

401(k)
Dental insurance
Health insurance
Paid time off
Vision insurance

Work Location: In person

Mass Institute of Clinical Research / Ki-Health Partners, LLC

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Clinical Research Coordinator