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Clinical Research Coordinator I Registered Nurse Jobs

Clinical Research Coordinator I
By Seattle Childrens Hospital At , Seattle, 98105, Wa $55,765 - $83,637 a year
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: -
Registered Nurse I Jobs
By Illinois Department of Human Services At , Park Forest, 60466, Il $5,274 - $7,155 a month
Competitive Group Insurance Benefits including Health, Life, Dental and Vision Insurance
4. Requires the ability to utilize office equipment, including personal computers and basic computer skills.
As a State of Illinois Employee, you will receive a robust benefit package that includes the following:
For more information about our benefits please follow this link:
3 Paid Personal Business Days annually
12 Paid Sick Days annually (Sick days carry over from year to year)
Registered Nurse I Jobs
By Illinois Department of Human Services At , Alton, 62002, Il $5,274 - $7,260 a month
6. Completes mandatory nursing training requirements and continuing education workshops and seminars to maintain professional competency.
Competitive Group Insurance Benefits including Health, Life, Dental and Vision Insurance
6. Requires the ability to utilize office equipment, including personal computers and basic computer skills.
As a State of Illinois Employee, you will receive a robust benefit package that includes the following:
For more information about our benefits please follow this
3 Paid Personal Business Days annually
Clinical Research Nurse Coordinator
By Lightship At , Richmond, Va $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
Clinical Research Coordinator I
By Inova Health System At , , Va
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
Clinical Research Coordinator I-Psychiatry-Msh-Ft-Day
By Mount Sinai Health System At United States
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.
Clinical Nurse I Jobs
By Covenant Health At Knoxville, TN, United States
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.
Research Coordinator I Jobs
By University of Southern California At Los Angeles, CA, United States

USC's Keck School of Medicine, Department of Medicine is seeking a Research Coordinator to join its team. The Research Coordinator is responsible for coordinating assigned projects. The Research ...

Clinical Research Coordinator I-Tisch Cancer Institute
By Mount Sinai Health System At United States
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.
Clinical Research Coordinator I-Personalized Med
By Mount Sinai Health System At United States
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.
Clinical Research Coordinator I-Emergency Med
By Mount Sinai Health System At United States
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.
Clinical Research Coordinator I-12910-049
By Mount Sinai Health System At United States
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.
Clinical Nurse I Jobs
By Covenant Health At Lenoir City, TN, United States
Completes nursing history and initiates patient education.
Demonstrates competence in performing critical skills to include appropriate delivery of care according to the age-specific needs of the population served.
$5k Sign-on Bonus for Experienced RNs
Correlates patient history and support systems across continuum of care.
Collaborates with interdisciplinary teams making recommendations to facilitate patient care.
Implements plan of care appropriate to diagnosis and patient needs. Evaluates outcomes.
Clinical Research Coordinator I (All Of Us)
By Mount Sinai Health System At United States
Strong communication and organization skills
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
Background in clinical research or closely related field
Passion for patient care and clinical research
Clinical Research Coordinator I-Psychiatry-Ism-Ft-Day
By Mount Sinai Health System At United States
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.
Clinical Research Coordinator I - Light & Health Research Center
By Mount Sinai Health System At United States
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.
Clinical Research Coordinator I - Personalized Med
By Mount Sinai Health System At United States
Obtain informed consent and educate participants regarding study requirements.
Strong communication and organization skills
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.
Clinical Research Coordinator I - Neurology
By Mount Sinai Health System At United States
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.
Registered Nurse - Clinical Leader
By State University of New York Upstate Medical University At Syracuse, NY, United States

Job Summary: The Clinical Leader provides operations based support to the nursing unit and exemplifies the Upstate mission, vision, and values acting in accordance with Upstate policies and ...

Clinical Research Coordinator I - Tisch Cancer Institute
By Mount Sinai Health System At United States
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.
1-2 years of research experience
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.