Clinical Research Nurse New

Job Title: Clinical Research Nurse

Location: Tampa, FL

Job Summary:

We are seeking a dedicated and compassionate Clinical Research Nurse to join a client of ours in Tampa, FL. This is a unique opportunity for a licensed Registered Nurse (RN) who is eager to transition into the exciting field of clinical research. Prior experience in clinical research is not required, but candidates should have a strong interest in learning and growing within the industry. The ideal candidate will play a key role in ensuring the safety, care, and well-being of study participants while supporting research protocols and compliance requirements.

Key Responsibilities:

• Assist in the coordination and implementation of clinical research studies while ensuring compliance with study protocols and regulatory requirements.
• Provide patient care, including monitoring and assessing study participants throughout the research process.
• Collect and document data accurately in case report forms (CRFs) and electronic data capture (EDC) systems.
• Educate patients and their families on study procedures, potential risks, and benefits.
• Work collaboratively with principal investigators, study coordinators, and other research staff to ensure smooth study operations.
• Administer investigational drugs and treatments as required by the study protocol.
• Maintain accurate and organized records for audits and regulatory submissions.
• Ensure patient safety by identifying and reporting adverse events in a timely manner.
• Stay current with Good Clinical Practice (GCP) guidelines, institutional policies, and industry best practices.

Qualifications & Requirements:

• Active Registered Nurse (RN) license in the state of Florida (required).
• Bachelor of Science in Nursing (BSN) required.
• Strong clinical skills with experience in patient care, IV administration, and medication management.
• Excellent organizational skills with keen attention to detail.
• Strong communication and interpersonal skills to work effectively with patients and research teams.
• Ability to adapt to a fast-paced, evolving research environment.
• Proficiency in electronic medical records (EMR) systems and Microsoft Office Suite.
• Prior exposure to clinical trials, research methodologies, or regulatory compliance is a plus but not required.