About the Role: Ki Health Partners is looking for a passionate and detail-oriented Clinical Research Coordinator to join their growing team in New Haven, CT. This is an exciting opportunity to play a meaningful role in advancing clinical research and improving patient outcomes. If you thrive in a fast-paced, science-driven environment, we want to hear from you!
Responsibilities:
Coordinate and manage day-to-day clinical trial operations in compliance with GCP and regulatory guidelines
Screen, enroll, and follow up with study participants throughout the duration of clinical studies
Collect, record, and maintain accurate study data using electronic data capture (EDC) systems
Serve as a primary point of contact for study sponsors, IRBs, and research staff
Prepare and submit regulatory documents, including IRB submissions, amendments, and continuing reviews
Monitor patient safety and report adverse events in accordance with protocol requirements
Support site initiation visits, monitoring visits, and audits conducted by sponsors or regulatory agencies
Requirements:
Bachelor's degree in life sciences, healthcare, or a related field
Minimum 3–5 years of experience in clinical research coordination or a similar role
Familiarity with FDA regulations, ICH-GCP guidelines, and IRB processes
Proficiency with EDC systems and clinical trial management software (CTMS)
SOCRA or ACRP certification (CCRP or CCRC) preferred
Strong organizational skills with exceptional attention to detail
Excellent interpersonal and communication skills for working with patients and multidisciplinary teams
About Us: Ki Health Partners is a forward-thinking healthcare organization dedicated to driving innovation in clinical research and patient care. Our team is committed to fostering a collaborative, mission-driven culture where every employee's contributions make a real difference. At Ki Health Partners, you'll find a supportive environment that values professional growth, scientific excellence, and meaningful impact.