We are seeking a dedicated and detail-oriented Clinical Research Coordinator to join our team (RN or LPN)  In this role, you will be responsible for overseeing clinical trials and ensuring compliance with regulatory standards. You will work closely with research teams, participants, and sponsors to facilitate the successful execution of clinical studies. The ideal candidate will possess a strong understanding of medical terminology, data management systems, and compliance management.

Responsibilities

• Coordinate and manage all aspects of clinical trials from initiation to completion.
• Conduct blood sampling and ensure adherence to safety standards.
• Oversee data collection processes, ensuring accuracy and integrity of data.
• Review documentation for compliance with regulatory requirements and study protocols.
• Maintain up-to-date knowledge of HIPAA regulations and ensure participant confidentiality.
• Collaborate with investigators to develop study protocols and informed consent documents.
• Monitor trial progress, addressing any issues that arise during the study.
• Prepare reports on study findings and assist in the publication of results.

Requirements

• Nursing degree in a relevant field (e.g., life sciences, nursing).- Recommended not preferred
• Experience in clinical development or related field preferred.
• Strong knowledge of medical terminology and clinical research practices.
• Proficiency in data management systems and documentation review processes.
• Excellent organizational skills with attention to detail.
• Ability to work independently as well as part of a team.
• Strong communication skills, both verbal and written.
• Familiarity with compliance management practices in clinical research.

Join us in advancing medical knowledge through rigorous research while ensuring the highest standards of participant care and data integrity.