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Clinical Research Nurse
2 months ago
Catalina Research Institute (CRI), an ACRS company, is a leading provider of Phase I-III clinical trials in complex metabolic and central nervous system indications. We are seeking a skilled Licensed Vocational Nurse (LVN) to join our team.
Job Summary:The Per Diem Clinical Licensed Vocational Nurse provides nursing standard of care in a research environment, responsible for monitoring study participants, collecting and reporting data on changes in their physical and mental status, monitoring drug action and side effects, collecting lab sampling, dispensing, and accounting for investigational product assigned.
Key Responsibilities:- Obtains, processes, and ships laboratory samples as per protocol.
- Assists and supports patient education on completion of diary, questionnaires, and logs required in trial (if applicable).
- Provides nursing standard of care in subjects admitted and seen in a clinical research setting, with the supervision of clinical research nurse-registered nurse (when applicable).
- Ensures subjects' safety and compliance with the protocol specific lifestyle guidelines.
- Obtains and maintains intravenous access on subjects admitted.
- Administers investigational product.
- Assesses adverse events and drug reactions – seeks medical intervention for patients when appropriate.
- Reports all adverse events (AEs), and serious or unexpected adverse events (SAEs) to the investigator and assisting the Investigator in reporting to the Sponsor/IRB all AEs/SAEs, as the protocol and regulations require.
- An LVN (or RN) license.
- Previous research experience and/or background are preferred.
- Research Nurse is expected to maintain nursing license, ACLS certification for LVN or RNs, and a working knowledge of, and assure compliance with, applicable ICH Guidelines, Good Clinical Practices.
- Excellent communication skills.
- Critical thinking skills.
- Planning/Organizational Skills.
- Personal Motivation.
- Customer Service Skills.
- Technical Competency Requirements:
- Understanding of ICH/GCP guidelines for human research.
- Understanding of Code of Federal Regulations for Human Subject.
- Computer Competency in Electronic Data Capture.
- Understanding Phases I-IV drug development process.
- ECG, Phlebotomy skills, and other technical skills related to completion of study visits as required by the protocol.
- No Travel required.
- Exposure to human bodily fluids.
- Laboratory Processing Procedures.
- Subject/Patient Care.
- Mid-level Computer Use.
- Weekend work schedules as needed.
- Work is normally performed in a typical interior clinical/office environment.
- Lifting of twenty pounds and occasionally more than twenty pounds.
ACRS Holdings is a leading provider of clinical research services, with a strong commitment to excellence and patient care. We are dedicated to advancing medical knowledge and improving patient outcomes through innovative research and development.
