Clinical Research Coordinator - Frontotemporal Disorders Unit - Remote

Overview

The Clinical Research Coordinator will assist in clinical research studies by recruiting and evaluating patients, collecting data, and performing clinical tests while ensuring compliance with established protocols.

In Short

• Assist in recruiting patients for clinical trials.
• Evaluate and consent patients for studies.
• Collect and organize patient data.
• Schedule patients for study visits.
• Perform clinical tests such as phlebotomy and EKGs.
• Maintain and update study data.
• Document patient visits and procedures.
• Assist with regulatory submissions and QA/QC procedures.
• Ensure compliance with sponsor and organizational guidelines.
• Prepare data for analysis and entry.

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 work collaboratively.
• Good interpersonal and communication skills.
• Computer literacy and knowledge of clinical research protocols.
• Respect and professionalism towards subjects' rights.

Benefits

• Opportunity to work with a leading medical institution.
• Engagement in groundbreaking medical research.
• Supportive and collaborative work environment.
• Comprehensive training and professional development.
• Access to resources and tools to enhance job performance.