Job DetailsJob Location
- Corporate
- Headquarters -
- West
- Bend,
- WI 53095Position
- Type:
- Full
- TimeSalary
- Range: $35.00 - $45.00
- HourlyJob
- Shift:
- DayTHIS
- IS
- A
- FULL
- TIME
- AM
- Position - 6am - 6pm
- Job
- Summary: Responsible for basic nursing activities (such as, but not limited to, presenting Informed Consents, documenting medical history, Adverse Events (AE), Concomitant Medications (CM), performing 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 (ICF) and that all questions have been answered. Accurately documents and records completion of ICF. Obtains and accurately documents structured subject medical, surgical and medication history. Performs venipuncture, capillary, and/or IV specimens from study participants 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.) study participants samples. 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. 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 staff members 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 additional task list items as delegated and supervised by Charge Staff or supervisor. 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 the progress of study participants 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. Trains staff in processes and procedures as needed. 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. Other functions as directed and delegated. The Statements made in the job description are intended to describe the general nature and level of work being performed by people assigned to this job. These statements are not intended to be an exhaustive list of all responsibilities, duties and skills required of people assigned to this job. 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: The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of the job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. 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 and ACLS 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. Qualifications
