Nurse Clinical Research I Jobs

Bilingual skills to communicate effectively with patients and families Understanding of JCAHO requirements

1 year of outpatient and inpatient clinical nursing experience in adult acute care

• Clinical Research Certification • Basic Life Support • Advanced Cardiac Life Support

Background Check and Live Scan

Legal Right to work in the United States

California Child Abuse and Neglect Reporting Act

Bachelor's Degree in related discipline, or equivalent combination of education and experience.

Prior experience in research or a related field/setting.

Confirmed proficiency in a second language via successful completion of a language assessment may be required for certain departments.

Min to Max Hourly Salary$26. 81 - $40.21 /hr

Min to Max Annual Salary$55,764.80 - $83,636.80 /yr

The union pay ranges can be found on the Seattle Children's website here: -

Seeks knowledge and competence that reflects current nursing practice and promotes futuristic thinking.

Collects data pertinent to the healthcare consumer's health or the situation.

Analyzes the assessment data to determine actual or potential diagnoses, problems, and issues.

Identifies expected outcomes for a plan individualized to the healthcare consumer or the situation.

Develops a plan that prescribes strategies to attain expected, measurable outcomes.

Implements the identified plan, coordinates care delivery, and employs strategies to promote health and a safe environment.

Required knowledge, skills, and abilities

Knowledge of medical terminology, drug calculation skills, and clinical medicine

Bachelor of Nursing or another Science degree preferred, or requisite combination of education, training, and experience

Administering investigational medications or providing patient education regarding administration, as necessary

Documenting study data in patient records (paper and electronic, as applicable) to capture protocol requirements

Participating in recruitment and selection of study patients by interviewing and documenting medical history / medication history per protocol requirements

Explains and performs non-GCP related study management activities.

Competitive salary: Pay based experience

Two years patient care experience or one year clinical research experience with a bachelor's degree

Masks are provided to patients entering our buildings, and offered free to visitors

What We Have to Offer

See Full List of Benefits Here: 2022 INOVA BENEFITS GUIDE

Medicare Part B Appeals experience preferred.

Job Family: Medical and Clinical

Conducts investigations and reviews of member and provider grievances and appeals.

Generates appropriate written correspondence to providers, members, and regulatory entities.

Ensures that appeals and grievances are resolved timely to meet regulatory timeframes.

Adapts to a wide variety of medical review topics in Part B appeals.

Medicare Part B Appeals experience preferred.

Job Family: Medical and Clinical

Conducts investigations and reviews of member and provider grievances and appeals.

Generates appropriate written correspondence to providers, members, and regulatory entities.

Ensures that appeals and grievances are resolved timely to meet regulatory timeframes.

Adapts to a wide variety of medical review topics in Part B appeals.

Recognize, investigate and refer abnormal findings to Clinic Manager and/or Medical Director, as appropriate.

Provide assistance, as needed, to the PIC clinic and administrative managers.

Perform study procedures as outlined in the study protocol, from recruitment to consenting, eliciting medical and health history and determining eligibility.

Perform study assessments dictated by protocol to include vital signs, body measurements, ECG, and other required study procedures.

Prepare and participate in monitoring visits.

Assist during Code Blue Emergency.

Completes nursing history and initiates patient education.

Collaborates with interdisciplinary team members.

Implements plan of care appropriate to diagnosis. Evaluates care outcomes.

Problem solves and coordinates unit/patient care assignments, with supervision.

Introduces new employees/students to unit routines.

Supervises LPNs, Nursing Assistants, HUCs, Techs and sitters.

Good organizational and time management skills

Or an equivalent combination of education and experience to successfully perform the key responsibilities of the job

To manage sites to ensure subjects are complying with protocol requirements, study visits, and timelines

Perform other duties as assigned by management

To facilitate translation and back translation of all necessary documents, as appropriate for local country requirements, as needed regionally

Good communication skills, oral and written

Knowledge of clinical research study processes, protocol management, and regulatory guidelines.

Proficiency in medical terminology and computer skills.

Strong attention to detail and excellent written and oral communication skills.

Ability to manage multiple deadlines and prioritize tasks effectively.

Minimum three years of experience in conducting clinical research studies or verifying clinical data.

Knowledge across multiple therapeutic areas, including blood and marrow transplant.

Assists with coordination and management of clinical trials including communication with Sponsors.

Under direct supervision of the Principle Investigator(s), obtains informed consent and educates participants regarding study requirements.

0-2 years of experience in a hospital or academic (research) environment preferred.

Excellent written and oral communication skills

Collects and records study data; inputs all information into database.

Secures, delivers and ships clinical specimens as required by the protocol.

Excellent organizational, time management, and problem-solving skills.

Support and comply with the company’s Quality Management System policies and procedures.

Basic proficiency of ICH GCP and monitoring practices with a track record for ensuring quality data and performing outstanding site management.

Supports the Clinical Study Manager to develop study-specific training materials.

Conducts thorough site qualifications visits. Ensures all required information concerning site/staff qualifications is clearly documented and communicated to project teams.

Works with clinical study manager to manage vendors (ie. Central Laboratory, CRF printers, CROs, etc).

Obtain informed consent and educate participants regarding study requirements.

1-2 years clinical research experience

Pristine attention to detail and ability to manage time appropriately, able to multitask in a fast-paced environment

Collect and record study data and input all information into a database.

Assist in IRB/GCO applications as needed.

Collect, process, deliver and ship clinical specimens as required by the protocol.

Obtains informed consent under minimal supervision of the investigator(s) and educates participants regarding study requirements.

1-2 years of research experience

Collects and records study data. Inputs all information into database.

Assists in preparing grant applications, IRB/GCO for submission and filings.

Secures, delivers and ships clinical specimens as required by the protocol.

Bachelors or Masters degree in Science or closely related field.

1+ years of Nursing experience

Utilize nursing assessment skills to observe participant general well-being and potential adverse events.

Active RN or LPN license in the state of Wisconsin

Enroll patients into clinical trials through the Informed Consent (ICF) process: educating, explaining and informing participants of study procedures.

Document adverse events and take appropriate action as needed.

Perform study-related activities such as vital signs, ECGs, and venipuncture.

Obtains informed consent under minimal supervision of the investigator(s) and educates participants regarding study requirements.

1-2 years of research experience

Collects and records study data. Inputs all information into database.

Assists in preparing grant applications, IRB/GCO for submission and filings.

Secures, delivers and ships clinical specimens as required by the protocol.

Bachelors or Masters degree in Science or closely related field.

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).

Must be detail-oriented and efficient in time management.

Conduct qualification, initiation, monitoring, and closeout visits at research sites in compliance with the approved protocol.

Verify adequate investigator qualifications, training and resources, including facilities, laboratories, equipment, and staff.

Assess the clinical research site’s patient recruitment and retention success and offering suggestions for improvement; and

Basic knowledge in regulations for applicable geographies and types of studies (IDE, non-significant risk, feasibility, exempt, etc.).

Minimum 1-year clinical research experience required.