About The Position

The Clinical Research Coordinator assists in the daily activities of clinical research studies, obtains informed consent; collects, maintains and organizes study information. Assists in preparing grant applications and documents (for e.g., Institutional Review Board, Grants and Contracts Office). We are seeking a highly motivated and organized Clinical Research Coordinator (CRC) to join our research team. The CRC will play a critical role in supporting two NIH-funded clinical research projects by focusing on patient recruitment, participant engagement, and coordination of study-related meetings. This position offers the opportunity to contribute to groundbreaking research while working closely with faculty investigators, research staff, and study participants

Requirements

  • Bachelors or Masters degree in Science or closely related field.
  • 1-2 years of research experience
  • Strong communication, organizational, and interpersonal skills.
  • Ability to manage multiple priorities and work independently as well as part of a team.

Nice To Haves

  • Prior experience in clinical research, patient recruitment, or healthcare setting (preferred).
  • Familiarity with IRB processes, research ethics, and HIPAA compliance (preferred).

Responsibilities

  • Patient Recruitment & Enrollment Identify, screen, and recruit eligible patients into study protocols.
  • Obtain informed consent in compliance with institutional and federal guidelines.
  • Serve as a primary contact for participants, ensuring a positive research experience.
  • Study Coordination Schedule and coordinate study-related meetings, including with investigators, study staff, and collaborators.
  • Maintain accurate and timely study records, logs, and regulatory documentation.
  • Assist with scheduling participant visits, follow-up calls, and reminders.
  • Communication & Collaboration Act as a liaison between participants, investigators, and the research team.
  • Coordinate with clinical and administrative staff to ensure smooth study operations.
  • Provide regular updates to the principal investigators and project managers.
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