Nurse Clinical Research I Jobs in Orange, California

Specialty Nursing Units: experience or specialty or ability to successfully complete a training program

Active, Current CA RN License

Qualified bilingual or multilingual candidates

Additional requirements for specific departments are as follows:

All Clinical Nurse I's are required to have current current BLS certification prior to clinical rotation.

Outpatient Treatment Centers Infusion (Non-Oncology) Chemotherapy/biotherapy certification preferred. ONSONCC

Registered Nurse in the State of California - Current and in good standing.

Oncology/Pulmonary/Sepsis: ACLS upon hire. Chemotherapy & Immunotherapy Provider Card required to administer chemotherapy.

Continuously assess safety improvement opportunities and communicate to departmental management.

Proactively communicate issues and/or problem resolutions to departmental supervisors and managers.

Degree from accredited Registered Nurse, Paramedic or equivalent program required. Related work experience preferred.

Current BLS certification - required

Physical Requirements & Working Conditions

Perform scheduled inspection of emergency crash carts, inventory/inspect the contents and maintain up to date records.

Neurosciences: Fulfills mandatory stroke education requirements per certification agency

Minimum of 5 years’ experience in nursing and 3 years’ of experience in area of specialty required.

Additional department specific requirements are as follows:

Registered Nurse in the State of California - Current and in good standing.

Neurosciences (Stroke): AANN (American Association of Neuroscience Nurses): SCRN or CNRN or ANVC (Association of Neurovascular Clinicians): NVRN-BC or ASC-BC

Salary Range: $52.7700 - $81.7400 /hour

Additional skills and knowledge of various equipment and software may be required.

A minimum of two to three (2 to 3) years of clinical nurse experience in a Medical Surgical/Telemetry unit.

Certification in a nursing specialty.

Administering medications and intravenous therapy with the ability to assess the appropriate indication dosing and effects of the medication administered.

Competitive 401 (k) program with matching contributions

Generous Paid Time Off (PTO)

Provides medication management services to clients with mental or emotional disorders

Provides case management services to selected clientele

Provides patient counseling and education related to clinical care needs

No first-time homebuyer requirement to qualify.

Orders and stocks clinic supplies and medications

Administers psychotropic medications and monitors side effects

Experience may substitute for minimum education requirements

Basic education, experience and skills required for consideration:

Preferred education experience and skills:

Conducts protocol management for an assigned set of multiple research protocols.

Performs data management and data analyses, as required by the research study.

Identifies and communicates important protocol and data management issues or problem areas to supervisor.

With supervision, assist in the accurate and appropriate study test article management.

Support the effective financial management of the clinical trial.

Other duties as assigned by appropriate management.

Assist in the identification and procurement of equipment and supplies needed to fulfill protocol requirements.

With guidance from the PI, communicate with and educate the research participant about study activities and requirements, as needed.

No supervisory responsibilities. May oversee specific tasks of non-licensed clinical trial research staff and provide feedback to supervisor.

Participates in required training and education programs.

1-year Clinical Research Related Experience

Join our team and use your skills with an organization known nationally for excellence in research!

Works with a Clinical Research Coordinator, Research Program Administrator or Research Nurse to coordinate/implement study.

Evaluates and abstracts clinical research data from source documents.

Ensures compliance with protocol and overall clinical research objectives.

Participates in required training and education programs.

Understanding of general clinical research objectives. One (1) year of clinical research experience is preferred.

Ability to interpret and apply knowledge of State, Federal and Agency standards to comply with regulations.

Must possess computer skills, including Word and Excel, and the ability to use standard office equipment is required.

Assists with clinical trial budgets and patient research billing.

Completes Case Report Forms (CRFs).

Participates in required training and education programs.

Works with a Clinical Research Coordinator, Research Program Administrator or Research Nurse to coordinate/implement study.

Evaluates and abstracts clinical research data from source documents.

Ensures compliance with protocol and overall clinical research objectives.

Completes Case Report Forms (CRFs).

Enters clinical research data into Electronic Data Systems (EDCs) that are provided by the sponsors.

Participates in required training and education programs.

1 year of Clinical Research Related Experience preferred

Works with a Clinical Research Coordinator, Research Program Administrator or Research Nurse to coordinate/implement study.

Evaluates and abstracts clinical research data from source documents.

Ensures compliance with protocol and overall clinical research objectives.

Completes Case Report Forms (CRFs).

Participates in required training and education programs.

Experience in a similar position is highly preferred.

Maintains the accuracy, integrity and security of complex, large computerized records systems.

Understands regulations, policies, protocols, and procedures to control and maintain accurate records.

Performs data searches and other related administrative tasks.

Ensures compliance with all federal and local agencies including the Food and Drug Administration (FDA) and local Institutional Review Board.

2 years of related experience in supporting medical device clinical trials

Strong interpersonal and communication skills

Able to manage multiple tasks

Experience working directly with US and EU sites strongly desired

Experience working with clinical data and databases (desirable)

Act as a central contact for the clinical team for designated project communications, correspondence and associated documentation

May implement and coordinate department-wide initiatives such as research quality management or clinical trial recruitment efforts.

Participates in required training and education programs.

Provides clinical research expertise by participating in the design and implementation of research projects as needed by the department or institution.

Responsible for specific and assigned aspects of research infrastructure development and/or maintenance.

Coordinates research projects at an institutional or departmental level.

Communicates project status and improvement areas with leadership in a timely manner.

Recognizes and implements legal and ethical responsibilities and duties of registered nurses;

Seeks supervision and guidance in developing nursing skills, in performing procedures not yet mastered, and when functioning in unfamiliar situations.

Must possess and maintain the following certification(s) during employment:

For clinical specialty areas, must possess and maintain the following certification(s) during employment:

Utilize educational resources available for promoting self-learning;

Ability to perform physical skills required to deliver patient care;

Strong communication skills both verbal and written, report writing, and ability to meet deadlines

Good team member and experience in working in an office environment

LPN with current state licensure at the time of hire and three (3) years of related work experience

Experience working on a research study or clinic is preferred, but not required

Experienced with research coordination and teams

Ability to acquire and maintain all required CITI training certificates

2 years of related experience in supporting medical device clinical trials

Strong interpersonal and communication skills

Able to manage multiple tasks

Experience working directly with US and EU sites strongly desired

Experience working with clinical data and databases (desirable)

Act as a central contact for the clinical team for designated project communications, correspondence and associated documentation