Clinical Research Coordinator I/Ii
By Fred Hutch At Seattle, WA, United States
Minimum one year experience in a clinical research or cancer registry environment with regulatory or human research protections.
Demonstrated knowledge of how to synthesis study conduct.
Excellent organizational skills, attention to detail, ability to problem solve and to prioritize multiple competing tasks in a dynamic environment.
Collaborative focus is essential, as well as strong written and verbal communication skills, including computer skills.
Minimum two to three years’ experience in a clinical research or cancer registry environment with regulatory or human research protections.
Knowledge of clinical trials records, procedures, and computerized data processing systems. Demonstrated knowledge of how to synthesize study conduct.
Clinical Nurse I/Ii
By County of Calaveras At San Andreas, CA, United States
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
Clinical Research Coordinator I
By Fred Hutch At Seattle, WA, United States
Liaise with investigators, industry sponsors, and other study teams to ensure each clinical trial under your management operates efficiently
Willingness to positively adapt to changing environments, data systems, compliance requirements and general competing priorities from internal and external sources
Minimum one year experience in a clinical research or cancer registry environment with regulatory or human research protections.
Demonstrated knowledge of how to synthesis study conduct.
Excellent organizational skills, attention to detail, ability to problem solve and to prioritize multiple competing tasks in a dynamic environment.
Collaborative focus is essential, as well as strong written and verbal communication skills, including computer skills.
Clinical Nurse I - Birthing Suites - Ldrp
By Hoag Health System At Irvine, CA, United States

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

Clinical Research Coordinator I-Iii
By UAMS - University of Arkansas for Medical Sciences At Little Rock, AR, United States
Bachelor’s degree plus 3-5 years clinical research experience w/demonstrated proficiency in study planning/development, study coordination/management, and/or data collection, or
Associate’s degree plus 5 years clinical research experience w/demonstrated proficiency in study planning/development, study coordination/management, and/or data collection, or
High School diploma/GED plus 7 years clinical research experience w/demonstrated proficiency in study planning/development, study coordination/management, and/or data collection
Bachelor’s degree plus 5 years clinical research experience w/demonstrated proficiency in study planning/development, study coordination/management and data collection
Knowledge and skill with word processing, spreadsheet, database, and e-mail computer software (e.g., Microsoft Word, Excel, Access, Outlook)
UAMS offers amazing benefits and perks
Registered Nurse I/P Hemodialysis
By CareWell Health At , East Orange, 07018
Certifications required: BLS (American Heart Association)
Certification in Nephrology Nursing, Aphaeresis Nursing or both is highly encouraged
Hemodialysis and ICU work experience preferred
Current Registered Nurse license to practice in the state of NJ.
Position Type/Expected Hours of Work:
Must be willing to work holidays, weekends and provide additional coverage as needed
Research Coordinator I Jobs
By USC At , Los Angeles $29.98 - $34.00 an hour

USC Department of Surgery recruiting a Research Coordinator I. The Research Coordinator I will assist investigators and other staff with research studies in subject recruitment, data collection, ...

Clinical Research Nurse Coordinator
By Lightship At , Concord $50 - $65 an hour
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
Nurse Aide State Registered I
By Commonwealth of Kentucky At , Wilmore, 40390 $17.96 an hour
SPECIAL REQUIREMENTS (AGE, LICENSURE, REGULATION, ETC.):
Assist residents with personnel hygiene such as bathing, dental/Oral Care, Hair/Nail care.
Assist with meals and nourishment for residents requiring assistance and restorative dining.
Measure and records temperature, blood pressure, pulse and respiration, and height as instructed.
Collect and label specimens for laboratory analysis.
Nurse Aide State Registered I
Clinical Research Nurse Coordinator
By University of Alabama at Birmingham At , Birmingham
Collect, store, and manage study data and databases.
The nurses may perform the following duties and responsibilities
Measure vital signs and measure weight, height, etc.
Extract patient medical history information from the medical record.
Recruit, screen, consent, and enroll participants.
Perform testing visits and collect study data.
Clinical Nurse I Jobs
By University of Maryland Medical System At , Glen Burnie, 21061
Must meet all unit specific certification requirements: (PALS, ACLS, NRP)
Must complete all of the Nurse Residency Program Requirements
Ability to learn and use computer systems in order to manage patient information
Demonstrated effective interpersonal, verbal and written communications skills
Reports to Nurse Manager/Charge Nurse of unit to which assigned.
An Associate Degree in Nursing is required; Bachelor of Science from a College of Nursing is preferred.
Clinical Research Coordinator I
By Emory University At , Atlanta, 30322
Maintains data pertaining to research projects, completes source documents/case report forms, and performs data entry.
Performs related approved responsibilities as required.
(1.) High School Diploma or GED and three years of administrative support experience OR
(3.) Licensed as a practical nurse (LPN) and one year admin support or one year of licensed practical nursing experience OR
Handles or assists with administrative activities generally associated with the conduct of clinical trials.
Assists with patient recruitment. Attends study meetings.
Clinical Research Coordinator I
By The Geneva Foundation At , San Antonio, 78234 $43,800 - $58,800 a year
Computer skills including at least intermediate level experience with Excel and other Microsoft Office Software
Bachelors degree or equivalent work experience required
2-4 years experience in clinical research preferred
2-4 years non-profit, research, or healthcare experience desired
Knowledge of CFR, GCP and ICH guidelines
Promote safety and confidentiality of research participants at all times
Research Registered Nurse, Cardiology
By UT Southwestern At , Dallas, 75390

Patient and study management :

Clinical Trial Research Nurse I
By Kaiser Permanente At , San Francisco $148,200 - $191,730 a year
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.
Clinical Research Nurse Coordinator
By Odyssey Systems Consulting Group, Ltd. At , Portsmouth, 23708
Provide support to the Department Head of the CID, Directorate for Professional Education, and Naval Medical Center Portsmouth (NMCP).
Provide IRB/HRPP support to the PI in the development and implementation of recruitment strategies in accordance with IRB/HRPP requirements and approvals.
Experience supporting research protocols for IRB and Institutional Animal Care and Utilization Committee (IACUC)
Working knowledge of United States Federal government regulations regarding the conduct of human clinical research.
Clinical competence in application of professional nursing theory, practices, and skills for the care of pediatric and adult patients.
Skilled in counseling, providing guidance, and maintaining interpersonal relationships.
Clinical Research Coordinator I
By University of Alabama at Birmingham At , Birmingham
Be organized, show attention to detail, and have exceptional follow-through abilities.
Have clinical decision-making and assessment skills, enjoy face-to-face interactions with patients and study participants, and interfacing with investigators and clinicians.
Work Arrangement (final schedule to be determined by the department/hiring manager): Onsite
To collect and record preliminary data for clinical research programs.
To recruit and perform follow-up with research participants as protocols outline.
To schedule visits according to research protocols.
Clinical Registered Nurse Jobs
By Institute on Aging At , San Francisco, 94118 $48 - $56 an hour
Manages minor illnesses, injuries, and the stable chronic illnesses of participants, according to standard procedures.
Preference will be given to those with experience in public health nursing, work with elders and/or acute care nursing.
At least two years of nursing experience at the RN level.
This range does not include any additional equity, benefits, or other non-monetary compensation which may be included.
Implements, directs, supervises and evaluates nursing care for participants of the IOA PACE program.
Participates in the health assessment and examination of applicants and participants; serves as a member of the Intake and Assessment Team.
Clinical Research Coordinator I
By Velocity Clinical Research, Inc. At Covington, LA, United States
The Clinical Research Coodinator I conducts and manages clinical trials in accordance with the study protocol,GCP, and Velocity’s SOPs.
Conduct and manage clinical trials in accordance with the study protocol, GCP, ICH Guidelines and Velocity’s SOPs
Implement research and administrative strategies to successfully manage assigned protocols.
Create, collect, and submit regulatory documents to Sponsors and IRBs as required per protocol, GCP/ICH regulations, and IRB requirements.
Bachelor’s degree with 1 year of relevant experience in the life science industry OR
Associate’s degree with 2 years of relevant experience in the life science industry OR
Research Nurse I Jobs
By Baylor College of Medicine At , Houston, 77030
Answers queries in accordance with protocol requirements.
Basic Life Support (BLS) Certification.
One year of relevant experience.
Documents clinical research data in electronic data capture (EDC) and/or iMedidata Rave.
Provides outreach in the community to enhance enrollment.
Regularly provides updates, follows-up on projects and ensures deadlines are met by all stakeholders as required.