About The Position

IMA Clinical Research is advancing the science behind psychiatry, behavioral health, and central nervous system (CNS) conditions. As a Clinical Trials Coordinator, you will work alongside experienced investigators, managing study operations from enrollment through completion while serving as a steady, trusted presence for participants navigating complex conditions. This role is ideal for someone who thrives in a patient-facing environment and wants their organizational skills to translate into real clinical progress.

Requirements

  • 2+ years of experience coordinating clinical research studies
  • Phlebotomy proficiency required
  • Bachelor's degree required

Nice To Haves

  • Prior experience in CNS, mental health, psychiatry, psychology, neuroscience, or behavioral health research preferred
  • Strong organizational skills with the ability to manage multiple active studies at once
  • CCRC certification preferred but not required

Responsibilities

  • Oversee daily clinical trial activities, ensuring protocol compliance and study success
  • Coordinate participant scheduling, study procedures, assessments, and follow-up visits
  • Perform phlebotomy and assist with collection and processing of study specimens
  • Serve as the key liaison between study participants, investigators, sponsors, CROs, and monitoring teams
  • Maintain source documentation, case report forms, and study records with rigorous attention to quality and accuracy
  • Support site readiness for audits, monitoring visits, and regulatory reviews
  • Assist with safety reporting, adverse event documentation, and participant retention efforts

Benefits

  • Comprehensive medical, dental, and vision benefits
  • 401(k) with employer matching contributions
  • Paid time off, company holidays, and a floating holiday
  • Tuition reimbursement programs
  • Student loan repayment assistance
  • Paid parental leave
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