MUST have a background in nursing or working with nursesīenefits: this role is eligible for an annual bonus, benefits (dental, vision, medical) are available day one of workīase Pay Range: $85,000.00 - $105,000.00 annuallyĪctual salaries may vary within the range based on several factors including, but not limited to education, training, experience, professional achievement, and location.2- 3 years of clinical experience in an acute hospital setting or comparable experience in a clinical research environment is required.Current Basic Life Support (BLS) required.Current Advanced Cardiac Life Support (ACLS) required.RN licensure in California highly preferred.BSN preferred or relevant work experience.Understand how to review study protocols and pharmacy manuals (dosing instructions).Demonstrated competency in all research-related tasks.Excellent interpersonal, verbal and written communication skills.Have the ability to manage multiple and varied tasks with enthusiasm and prioritize workload with attention to detail.Possess knowledge and skills necessary to provide care appropriate to the age and/or indication of the study participants served.Ability to assess, monitor and respond to emergency situations.Proven emergency care and comprehensive assessment skills.Demonstrated leadership ability and critical thinking.Amenable to flexible working schedule as required by business and workflow, including shift rotations, weekend and evening work, on-call obligations, as well as an understanding that flexibility in work schedule is important to meet business needs.Be the main point of contact for the nurses on shifts to answer questions or assist with emergencies that may arise on shift.Maintain and update professional competencies, ensuring knowledge and understanding of Clinical Operating Guidelines and related hospital policies, as applicable.Obtain and/or support informed consent from trial participants according to GCP guidelines and SOP’s, as required.Ensure that all nursing and protocol-related procedures are completed and documented according to GCP and standard nursing practice. Respond, lead and assist in emergency and code situations by following standard emergency protocols and SOPs.Assist physician or perform more complex clinical procedures as required.Administer concomitant medication (all routes), give treatments and perform other medical procedures as prescribed by the physician (medical group).Maintain IP chain of custody in coordination with the Pharmacy. Proactively plan and prepare dosing procedures/instructions (for example, preparing the Dosing Information Sheet). Act as dosing nurse for studies and administer IP via any route as per protocol, nurse practice, clarifications and guidelines.Responsible for assessment, monitoring, recording, and reporting patient’s condition and reaction to drugs and treatments to the appropriate physician and CRC, and dispensing medication as directed.Responsible for ensuring study participant safety, identifying and responding to changes in the study participant’s physical, mental, and/or behavior to take appropriate action, and if necessary, notify physician and/or research team, documenting as required.Responsible for providing clinical/protocol related training to ensure understanding across the clinic floor, guiding and directing staff and others to ensure safety and protocol compliance.Responsible for upholding the protocol, SOPs and GCP in all work processes to ensure efficient and compliant clinical operation within the Early Phase Clinical Unit (EPCU), including but not limited to daily crash and medication cart checks recording, monitoring and following up with PI daily on Adverse Events (AE’s) and review, monitoring and following up on concomitant medications, discussing with PI as required.Responsible for patient and healthy study participant care and study conduct assignments. Charge nurse duties are assigned on a rotating basis
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