Clinical Research Coordinator I - Remote

Overview

The Clinical Research Coordinator I provides support to clinical research projects by assisting the Principal Investigator in various tasks including data collection, patient interaction, and maintaining study-related documentation.

In Short

• Assist in recruiting and consenting patients for clinical trials.
• Collect and organize patient data from various sources.
• Prepare data for analysis and maintain study records.
• Communicate study details clearly to patients and staff.
• Participate in the creation of study forms and questionnaires.
• Conduct library searches for clinical research information.
• Ensure compliance with study protocols and regulatory requirements.
• Document patient visits and procedures accurately.
• Train and supervise new Research Assistants.
• Act as a point of contact for communication with the Principal Investigator.

Requirements

• Bachelor's Degree in Science required.
• 0-1 year of relevant research project experience preferred.
• Attention to detail and good organizational skills.
• Ability to follow directions and communicate effectively.
• Computer literacy and knowledge of clinical research protocols.

Benefits

• Opportunity to work in a diverse and inclusive environment.
• Engagement in meaningful clinical research projects.
• Professional development and training opportunities.
• Supportive team environment.
• Contribution to advancements in medical research and patient care.