Clinical Research Nurse Job at SQRL, Tampa, FL

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  • SQRL
  • Tampa, FL

Job Description

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.

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