About The Position

Be Part of Breakthroughs That Change Lives. Are you ready to play a key role in advancing medicine and improving patient care through clinical research? As a Clinical Research Coordinator I, you’ll help bring innovative treatments from the lab to real people — coordinating and managing research studies that make a real difference. Working closely with our investigators, sponsors, and study participants, you’ll ensure every detail — from patient enrollment to regulatory documentation — meets the highest standards of ethics, accuracy, and care.

Requirements

  • Bachelor’s degree in an allied health or related field.
  • Strong organization and time management skills with the ability to manage multiple projects.
  • Excellent written and verbal communication skills.
  • Attention to detail and ability to work independently.
  • Proficiency with computer systems and documentation tools.

Nice To Haves

  • One year of clinical research experience.
  • Clinical Research Coordinator Certification (ACRP or SoCRA).
  • Working knowledge of GCP, FDA, and DHHS regulations, ICH Guidelines, and HIPAA.

Responsibilities

  • Coordinate every phase of clinical studies — from start-up and recruitment to completion — ensuring all activities follow Good Clinical Practice (GCP) and institutional policies.
  • Serve as a key liaison among investigators, sponsors, IRB, and study participants.
  • Manage research documentation, including regulatory files, informed consents, and case report forms.
  • Partner with investigators to prepare and submit protocols and amendments to the IRB.
  • Support the financial and administrative aspects of each study, working with leadership to ensure appropriate funding and compliance.
  • Maintain subject confidentiality and safety in accordance with HIPAA and research regulations.
  • Collaborate across departments to successfully launch new studies and support recruitment efforts.
  • Stay up to date on research ethics, regulatory changes, and institutional requirements.
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