What are the responsibilities and job description for the Pharmacy clinical research RN position at ENTRUST CLINICAL RESEARCH?
Company Description ENTRUST CLINICAL RESEARCH is a clinical research organization based in Miami, Florida, dedicated to advancing medical knowledge and patient care through high-quality clinical trials. Located at 10621 N Kendall Drive, the company partners with healthcare professionals, sponsors, and patients to conduct compliant and ethically sound research. ENTRUST CLINICAL RESEARCH focuses on delivering accurate data, maintaining patient safety, and adhering to regulatory standards. Team members work in a collaborative environment that supports professional growth, continuous learning, and meaningful contributions to evidence-based medicine.
Role Description The Pharmacy Clinical Research RN is a full-time, on-site role based in Miami, FL. This role is responsible for coordinating and administering study-related medications and treatments in accordance with clinical trial protocols and institutional policies. Daily responsibilities include assessing and monitoring study participants, documenting clinical data, managing investigational product handling, and ensuring accurate medication dispensing and reconciliation under protocol guidelines. The RN collaborates closely with investigators, pharmacists, coordinators, and other research staff to support patient enrollment, education, informed consent, and follow-up. Additional tasks include maintaining regulatory and source documentation, reporting adverse events, participating in study meetings, and contributing to quality assurance and continuous process improvement within the research team.
Qualifications
Role Description The Pharmacy Clinical Research RN is a full-time, on-site role based in Miami, FL. This role is responsible for coordinating and administering study-related medications and treatments in accordance with clinical trial protocols and institutional policies. Daily responsibilities include assessing and monitoring study participants, documenting clinical data, managing investigational product handling, and ensuring accurate medication dispensing and reconciliation under protocol guidelines. The RN collaborates closely with investigators, pharmacists, coordinators, and other research staff to support patient enrollment, education, informed consent, and follow-up. Additional tasks include maintaining regulatory and source documentation, reporting adverse events, participating in study meetings, and contributing to quality assurance and continuous process improvement within the research team.
Qualifications
- Strong clinical foundation in Nursing and Medicine, with the ability to apply evidence-based practice in a clinical research setting.
- Experience in Oncology Nursing or complex patient populations, including the safe administration and monitoring of specialized therapies, is preferred.
- Demonstrated competency in Research activities, including data collection, documentation, and adherence to study Protocol requirements.
- Active, unrestricted RN license in the state of Florida; BSN or higher degree in Nursing preferred.
- Prior experience in clinical research, hospital-based pharmacy services, or investigational drug studies is highly beneficial.
- Familiarity with Good Clinical Practice (GCP), FDA regulations, and institutional review board (IRB) processes.
- Excellent communication, collaboration, and patient education skills, with a strong attention to detail and documentation accuracy.
- Ability to work on-site full time, manage multiple studies and priorities, and use electronic medical records and research databases efficiently.