Clinical Research Nurse

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Clinical Research Nurse - 248944

Schedule:

Monday-Friday 8-5 onsite – paid weekly, benefits offered on contract.

Duration: 6‑month contract to full‑time hire with the client.

Oncology experience is a must even if it is outside of research.

Experience as a Clinical Research Nurse is a plus.

3 years of nursing experience ideally.

• Demonstrates knowledge of policies, procedures, and regulations governing human subjects research and incorporates them into the conduct of research and participant care.
• Maintains a working understanding of federal regulations related to the protection of human subjects, including FDA, OHRP, GCP/ICH guidelines, and HIPAA.
• Prepares and processes IRB submissions, including new study proposals, amendments, continuing reviews, and adverse event reports, in accordance with institutional, departmental, and federal requirements.
• Supports the management and execution of clinical trial operations across multiple studies.
• Learns and performs study‑specific protocol procedures, obtaining required training to ensure procedures are completed safely and accurately.
• Prepares, maintains, and organizes essential regulatory documents required before, during, and after clinical trial conduct.
• Packages and ships investigational product and biological specimens (e.g., blood, urine) in accordance with IATA and sponsor guidelines.
• Participates in sponsor, regulatory, and internal monitoring visits, supporting source documentation review and study compliance.
• Screens, evaluates eligibility, and recruits potential participants for clinical trial enrollment.
• Implements and troubleshoots recruitment strategies to support timely enrollment and completion of studies.
• Provides research‑specific education and training to staff and study participants as appropriate.
• Maintains professional, clear communication with investigators, participants, research staff, sponsors, and collaborating departments.
• Reviews complex clinical data to ensure documentation accuracy, completeness, and participant safety.
• Manages multiple studies and responsibilities simultaneously while meeting documentation and visit timelines.
• Distinguishes standard of care from research‑specific activities and assesses the need for additional participant protections.
• Applies clinical judgment and problem‑solving skills to identify participant or study issues and implements appropriate solutions.
• Actively participates in quality improvement initiatives through assessment, issue identification, and corrective action planning.
• Serves as an advocate for research participants by promoting ethical conduct and maintaining open communication with all stakeholders.
• Reviews medical histories and clinical data to ensure appropriate subject enrollment.
• Supports and participates in the informed consent process, ensuring participant understanding throughout study participation.
• Conducts study activities including recruitment, screening, scheduling, enrollment, assessments, interviews, laboratory and diagnostic procedures, medication dispensing, and protocol‑specific tasks.
• Independently documents and applies clinical processes to support safe, individualized care for uncomplicated research participants, with assistance for complex cases as needed.
• Performs research procedures per protocol, reporting deviations promptly when participant safety is at risk.
• Maintains accurate records of recruitment efforts, follow‑up communications, and research data.
• Identifies, documents, and reports adverse events to investigators and regulatory bodies in accordance with protocol and regulatory requirements.
• Conducts literature reviews and assesses new findings to evaluate potential impact on participant safety and study risk‑benefit profiles.
• Engages in ongoing professional development, training, and education to maintain and enhance research competency.
• Actively pursues learning opportunities and maintains required certifications, licensure, and credentials (e.g., CPR/BLS).
• Completes required research education and training within designated time frames.

• Mid‑Senior level

• Full‑time

• Research
• Hospitals and Health Care (Industry)

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