Job Title: Jr. Clinical Research Coordinator (Nurse)

Overview

We are currently seeking a passionate and dedicated Junior Clinical Research Coordinator (Nurse) to join our team of healthcare professionals and researchers. In this role, you will assist in the coordination, management, and execution of clinical research projects. You will work alongside a diverse and multidisciplinary team focused on advancing medical knowledge and improving patient outcomes. This is a fantastic opportunity to grow your career in clinical research while directly impacting patient care in an inclusive and supportive environment.

Responsibilities

• Assist with planning, coordinating, and executing clinical research studies while ensuring compliance with regulatory guidelines and protocols.
• Collaborate with investigators and other teams to recruit, screen, and enroll study participants, ensuring a respectful and informed consent process.
• Oversee patient care responsibilities during trials, such as monitoring participants’ health during the study period and assisting with any clinical procedures as needed.
• Ensure accurate collection, documentation, and recording of study data in compliance with Good Clinical Practice (GCP) standards.
• Assist in the preparation of study-related materials, including consent forms, study reports, and presentations.
• Act as a liaison between research sites, participants, and sponsors to facilitate effective communication and ensure consistent study progress.
• Monitor adherence to study protocols and provide problem-solving support for challenges encountered during the trials.
• Maintain thorough and up-to-date knowledge of clinical research regulations, including FDA guidelines and ethical research standards.
• Contribute to fostering an environment focused on patient safety, quality care, and staff collaboration.

Qualifications

• Education: Registered Nurse (RN) or equivalent with an active license in good standing. A Bachelor’s degree in Nursing (BSN) is preferred.
• Experience: Prior exposure to clinical research or clinical trials is highly desirable.
• Strong understanding of clinical research processes, protocols, and ethical guidelines.
• Excellent patient-facing skills, including empathy, communication, and the ability to build rapport with individuals from a wide range of backgrounds.
• Ability to work independently and as part of a collaborative team while meeting project deadlines.
• Strong organizational and multitasking abilities, with great attention to detail.
• Familiarity with data collection tools and electronic medical records (EMR) systems is a plus.
• Certified Clinical Research Coordinator (CCRC) or Clinical Research Professional (CCRP) certification is a bonus but not required.