Clinical Research Coordinator

Overview
We are seeking a dedicated and detail-oriented Clinical Research Coordinator to join our team. In this role, you will be responsible for overseeing clinical trials and ensuring compliance with regulatory standards. You will work closely with research teams, patients, and healthcare professionals to facilitate the successful execution of clinical studies. The ideal candidate will possess strong organizational skills, a solid understanding of clinical research processes, and the ability to manage multiple tasks efficiently.

Responsibilities

• Supervise and coordinate all aspects of clinical trials, including planning, implementation, and monitoring.
• Manage documentation review to ensure accuracy and compliance with Good Clinical Practice (GCP) guidelines.
• Monitor patient progress throughout the study, ensuring adherence to protocols and safety regulations.
• Collect and manage data from clinical trials, utilizing statistical software for analysis.
• Ensure compliance with FDA regulations and HIPAA standards in all research activities.
• Collaborate with clinical laboratory staff to facilitate blood sampling and other laboratory procedures.
• Conduct patient assessments, including vital signs monitoring and documentation of medical history.
• Maintain accurate records in Electronic Medical Record (EMR) systems and ensure data integrity.
• Assist in the development of study protocols and informed consent documents.
• Provide training and support to junior staff members on clinical trial processes.

Skills

• Supervising experience in a clinical research setting is preferred.
• Strong knowledge of clinical trials management, including phases of clinical development.
• Familiarity with medical terminology and documentation review processes.
• Experience in patient monitoring and data collection methodologies.
• Proficient in statistical software for data analysis and management.
• Understanding of FDA regulations related to clinical research.
• Clinical laboratory experience is a plus, particularly in phlebotomy and blood sampling techniques.
• Knowledge of CDISC standards for data submission is beneficial.
• Excellent analytical skills with attention to detail for compliance management.
• Ability to work collaboratively within a multidisciplinary team environment. Join us in advancing medical research through effective coordination of clinical trials. Your expertise will contribute significantly to improving patient outcomes and enhancing our understanding of medical treatments.

Job Type: Full-time

Pay: $25.00 - $35.00 per hour

Benefits:

• Flexible schedule
• Paid time off

Work Location: In person