Comprehensive Clinical Research, LLC Hiring for Clinical Research Coordinator at West Palm Beach, FL Full Time

Responsibilities for Clinical Research Coordinator

• Responsible for ensuring study compliance with local and federal laws and regulations
• Recruits and screens potential study participants and performs intake assessments
• Creates and/or maintains all documents and records related to the study
• Acts as a point of reference for study participants by answering questions and keeping them informed on the study progress
• Manages the inventory of equipment and supplies related to the study and orders more as needed
• Attends meetings, events and seminars in order to promote the study
• Inputs data and patient information
• Creates s on each study, including notes on protocols, workload, data collection, and more

Qualifications For Clinical Research Coordinator

• 1+ years previous experience working in a clinical setting
• Excellent written and verbal communication skills
• Superior organizational and time management skills
• Capable of working independently with minimal supervision and also as part of a team
• Skilled with standard computer programs including the MS Office suite
• Ability to speak a second language is an asset, but not required (Spanish Preferred, not required)
• Understanding of medical terminology as well as standard clinical procedures and protocols
• Ability to lift up to 20 pounds for a short period and capable of standing for extended periods of time

EMAIL RESUMES TO: JAckerman@ccrwpb.com

Company Description

We are a Clinical Research Site with experience in the field for 25 years.

We are a Clinical Research Site with experience in the field for 25 years.