Job Description

We are seeking an LPN Clinical Research Coordinator to join our clinical research team. The coordinator will work closely with other staff as a team player, maintaining flexibility and a thorough understanding of assigned protocols.

Responsibilities

• Collaborate effectively with other staff as a team player.
• Maintain flexibility in work duties and possess thorough knowledge of assigned protocols.
• Attend Investigators’ Meetings to learn study requirements and convey information to the site study team.
• Train site personnel and other medical staff in understanding and implementing protocols.
• Design and maintain organizational tools to conduct the study accurately in compliance with GCP and Protocol.
• Recruit and screen potential study participants according to protocol criteria.
• Conduct telephone screenings followed by visits to ensure continuity of subject care.
• Obtain proper written informed consent from study participants.
• Manage study participants’ visits and perform defined activities accurately.

Essential Skills

• Licensed Practical Nurse (LPN)
• Clinical research experience preferred
• Case management skills
• Bilingual (English & Spanish) preferred

Work Environment

The work environment is a 24-hour clinical research facility operating primarily on a day shift from 7:30 am to 4:00 pm, Monday through Friday, with a half-hour lunch break. Some overtime and weekend work may be required