RN

Job Details Job Location: Corporate Headquarters - West Bend, WI 53095 Position Type: Full Time Education Level: Not Specified Salary Range: $35.00 - $50.00 Hourly Travel Percentage: Negligible Job Shift: Graveyard Job Category: Health Care THIS IS A FULL TIME NOC POSITION RN SHIFT LEAD DESCRIPTION Job Summary: Responsible for advanced nursing activities such as, but not limited to, Informed Consent documentation, medical history, AE/CM, drug administration/accountability, dose verification, focused subject physical assessments, collaborate with the medical team, IV placement, IV infusions, vital signs, ECG lead placement in the conduct of clinical trials with emphasis on the safety and welfare of study participants. Performs the practical activities of clinical studies according to protocol, regulatory requirements, SOPs, scope of practice and current training status. Essential Duties and Responsibilities With supervision, ensures that clinical trials are conducted according to protocol requirements by utilizing the following techniques & procedures. Ensures subject has complete understanding of study-specific Informed Consent Form and that all questions have been answered. Accurately documents and records completion of Informed Consent. Obtains and accurately documents structured subject medical, surgical and medication history Performs meal administration, ensuring the correct meal and correct content is delivered to the correct study participant. Performs subject bag checks to ensure no contraband is present on study floor Performs study activities such as ECG positioning, exercises, or other study procedures requiring supervision of subjects. Performs venipuncture, capillary, and/or IV specimens from study subjects according to established protocol, maintains aseptic technique. Performs proper and accurate sample management, including collection, identification, transport, and/or processing of biological (blood, urine, etc) subject samples. Administers study drug and any other protocol-required medications, while accurately ensuring the 5 Rights of Medication Administration (the right subject, the right drug, the right dose, the right route, and the right time) Performs dose verification, assisting other Clinical Research Nurses during dose administration to accurately verify subject identity and dosing labeling, as additional quality check. Contributes and is accountable for secure and appropriate storage of all drug supplies after removing from pharmacy. Records subject Adverse Events with proper escalation to medical or Charge Staff for evaluation and treatment as warranted. Performs and records physical measurements including height, weight, and BMI calculation. Performs and records vital sign measurements (blood pressure, pulse oximetry, heartrate, temperature, respirations, etc). Places ECG electrodes and leads accurately to ensure precise telemetry monitoring. Performs additional task list items as delegated and supervised by Charge Staff. Reviews Study Specific Trainings and applicable protocols for a thorough understanding of the study procedures, as they apply to their role and ensures that Delegation of Authority/Training Log for each study is completed in a proper and timely manner. Keeps abreast of SOPs, Good Clinical Practice (GCP) and ICH guidelines, state and national laws and ethical standards. Observes and maintains all HIPAA, OSHA, and Exposure Control regulations and Emergency Response as required by applicable training. Creates and maintains accurate records of all protocol activities and events, as delegated and trained. Follows progress of volunteers and provides for their care, comfort and safety by attending to their needs during study participation. Participates in quality assurance of clinical research projects and initiates the need for same as it impacts on clinical practice. As required for study or site needs and if trained and delegated may be assigned study procedures such as obtaining participant information/histories/questionaries/meals/vital signs/EKGs/drug administration/specimen collection/luggage searches. Skills/Qualifications Ability to read, write and interpret the English language. Portrays professionalism in all interactions at Spaulding Clinical. Good computer skills; inclination to adopt technology to maximize efficiency Demonstrates strong analytical, problem solving skills Strong written and verbal communication skills. Detail oriented, good organizational traits. Self-motivated Must be results-oriented, multi-tasking, quick learner, respond to the urgent needs of the team, and show a strong track record of meeting deadlines. Ability to work beyond normal work hours and various shift availability required. Ability to perform and record data entry via computer systems while conducting timed clinical procedures. Physical Demands Ability to sit, stand, walk, reach with hands and arms, and use hands along with fingers, to handle or feel. Ability to lift and/or move up to 25 pounds. Specific vision abilities required by this job include clarity of vision both near and far. Ability to identify and distinguish colors. Hazards Potential for exposure to toxic or caustic chemicals Potential for exposure to blood borne pathogens Education and Experience Current RN or LPN License (Graduate Nurses must possess a temporary license in order to work as CRN, and must obtain Wisconsin licensure within 6 months of hire) BLS certification required within 6 months of hire or promotion date Spaulding Clinical Research management has the discretion to hire personnel with a combination of experience and education which may vary from the above listed skills and qualifications. ADDITIONAL CHARGE INFORMATION Job Summary Responsible for overseeing daily clinical operations on clinical study floor and ensuring all studies are conducted according to study protocols and Spaulding Clinical SOP’s. Works closely with Clinical Research Coordinators, Study Manager and Clinical Floor Supervisors to ensure studies are conducted according to study specific operational plans. Coordinates, organizes, monitors and delegates daily activities of Clinical Staff assigned to study floor events, ensures adherence to policies and procedures and provides leadership and professionalism in clinical problem solving. Essential Duties and Responsibilities Keeps abreast of SOP’s, ICH/GCP guidelines, NIH guidelines, as well as state and national regulatory requirements. Maintains calm, professional atmosphere on study floor, leading by example with professional resolution of conflict and appropriate delegation. Ensures that Study Manager and Clinical Floor Supervisors are updated and escalates study related issues that arise on the study floors with urgency, if needed. Communicates all other issues as warranted to the appropriate department. Records subjects Adverse Events with proper documentation and treatment as warranted and escalates to medical personnel or project management as appropriate. Administers oral study drug, while accurately ensuring the 5 Rights of Medication Administration (the right subject, the right drug, the right dose, the right route, and the right time) Performs dose verification, assisting other dosers during dose administration to accurately verify subject identity and dosing labeling, as additional quality check. Contributes and is accountable for secure and appropriate storage of all drug supplies after removing from pharmacy. Ensures all shift duties are completed according to Charge Checklist or equivalent, including completion of all applicable logs and metrics. Works with colleagues to achieve departmental goals as delegated. Maintains knowledge of company goals to assist all floor staff in their development and engagement. Maintains a clean, quiet study environment in all study areas. Works with Training Department to perform and document Process Monitoring to ensure staff compliance and adherence. As required for study or site needs and if trained and delegated may be assigned study procedures such as obtaining participant information/histories/questionaries/meals/vital signs/EKGs/drug administration/specimen collection/luggage searches. Skills/Qualifications Ability to read, write, and interpret the English language. Must show ability to stay up-to-date on all available trainings. Excellent time management skills. Demonstrates strong analytical and problem solving skills. Demonstrates effective leadership traits with ability to direct and delegate. Portrays professionalism in all interactions at Spaulding Clinical. Strong written and verbal communication skills. Self-motivated. Must be reliable and responsible for attending scheduled shifts, along with flexibility for higher study activity demands. Must be results oriented, proficient at multi-tasking, quick learner, organized, responsive to the urgent needs of the team and show a strong track record of meeting deadlines. Proficient computer skills; inclination to adopt technology to maximize efficiency. Strong attention to detail. Demonstrates ability to adapt to a rapidly changing study environment. Physical Demands Ability to sit, stand, walk, reach with hands and arms, and use hands along with fingers, to handle or feel. Ability to lift and/or move up to 25 pounds. Specific vision abilities required by this job include clarity of vision both near and far. Ability to identify and distinguish colors. Hazards Potential for exposure to toxic or caustic chemicals Potential for exposure to blood borne pathogens Education and Experience Medical background required, with skill set appropriate for role Must be trained (or in-training) as Clinical Research Technician - Advanced or Clinical Research Nurse - Advanced Has demonstrated effective professionalism, leadership, and problem-solving skills as clinical floor staff for approximately 6 months at Spaulding Clinical, OR exceptional outside experience (previous charge, supervisory and/or leadership position) that would translate to a Charge role immediately upon hire CPR certification required within one year of hire or promotion date ACLS certification may be required within one year of hire or promotion date Spaulding Clinical Research management has the discretion to hire personnel with a combination of experience and education which may vary from the above listed skills and qualifications. #J-18808-Ljbffr