Advanced Nurse Practitioner-Sub investigator
Medical Research
40–50 an hour
Behavioral Health Market Context
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Job Description
ic laboratory procedures, standards of Good Clinical Practice (GCP), Standard Operating Procedures (SOPs), quality (QA/QC) procedures, OSHA guidelines, and other state and local regulations as applicable.
Responsibilities included but not limited to:
• Ensures informed consent has been obtained prior to performing any study procedures
Performs all study responsibilities in compliance with the IRB approved protocol
• Reviews screening documentation and approves subjects for admission to study
• Reviews admission documentation and approves subject for randomization
• Documents all findings in subject specific source documents
• Provides ongoing assessment of the study subject/patient laboratory reports to identify Adverse Events
• Ensures proper documentation and reporting of all Adverse Events and Serious Adverse Events
• Reviews and evaluates all study data and comments to the clinical significance of any out of range results
• Performs physical examinations as part of screening evaluation and active study conduct
• Provides medical management of adverse events as appropriate
• Monitors safety and well-being of study participants at all times
• Performs any psychological examinations required
• Participates in any meetings required by the sponsors
• Ability to perform physical and neurological examinations
• Ability to interpret laboratory results and ECG readings
• Ability to perform IV administrations and SC injections
Job Types: Part-time, Per diem
Pay: $40.00 - $50.00 per hour
Benefits:
• Flexible schedule
Application Question(s):
• What days and times do you have available to work each week?
Education:
• Master's (Required)
Experience:
• Advanced practice provider: 1 year (Preferred)
Language:
• Spanish (Required)
License/Certification:
• ACLS Certification (Preferred)
• Medical License (Required)
Ability to Relocate:
• Miami Lakes, FL 33015: Relocate before starting work (Required)
Work Location: In person
Responsibilities included but not limited to:
• Ensures informed consent has been obtained prior to performing any study procedures
Performs all study responsibilities in compliance with the IRB approved protocol
• Reviews screening documentation and approves subjects for admission to study
• Reviews admission documentation and approves subject for randomization
• Documents all findings in subject specific source documents
• Provides ongoing assessment of the study subject/patient laboratory reports to identify Adverse Events
• Ensures proper documentation and reporting of all Adverse Events and Serious Adverse Events
• Reviews and evaluates all study data and comments to the clinical significance of any out of range results
• Performs physical examinations as part of screening evaluation and active study conduct
• Provides medical management of adverse events as appropriate
• Monitors safety and well-being of study participants at all times
• Performs any psychological examinations required
• Participates in any meetings required by the sponsors
• Ability to perform physical and neurological examinations
• Ability to interpret laboratory results and ECG readings
• Ability to perform IV administrations and SC injections
Job Types: Part-time, Per diem
Pay: $40.00 - $50.00 per hour
Benefits:
• Flexible schedule
Application Question(s):
• What days and times do you have available to work each week?
Education:
• Master's (Required)
Experience:
• Advanced practice provider: 1 year (Preferred)
Language:
• Spanish (Required)
License/Certification:
• ACLS Certification (Preferred)
• Medical License (Required)
Ability to Relocate:
• Miami Lakes, FL 33015: Relocate before starting work (Required)
Work Location: In person
Qualifications
- •Ability to perform IV administrations and SC injections
- •Master's (Required)
- •Spanish (Required)
- •Medical License (Required)
- •Miami Lakes, FL 33015: Relocate before starting work (Required)
Benefits
- •Pay: $40.00 - $50.00 per hour
- •Flexible schedule
Responsibilities
- •(2-6 hours per day)
- •ARNP will be assigned as a sub-investigator to work closely with the Principal Investigator of all clinical trials assigned
- •ARNP will help to oversee the execution of study protocols, delegating study related duties to site staff, as appropriate, and ensuring site compliance with study protocols, study-specific laboratory procedures, standards of Good Clinical Practice (GCP), Standard Operating Procedures (SOPs), quality (QA/QC) procedures, OSHA guidelines, and other state and local regulations as applicable
- •Ensures informed consent has been obtained prior to performing any study procedures
- •Performs all study responsibilities in compliance with the IRB approved protocol
- •Reviews screening documentation and approves subjects for admission to study
- •Reviews admission documentation and approves subject for randomization
- •Documents all findings in subject specific source documents
- •Provides ongoing assessment of the study subject/patient laboratory reports to identify Adverse Events
- •Ensures proper documentation and reporting of all Adverse Events and Serious Adverse Events
- •Reviews and evaluates all study data and comments to the clinical significance of any out of range results
- •Performs physical examinations as part of screening evaluation and active study conduct
- •Provides medical management of adverse events as appropriate
- •Monitors safety and well-being of study participants at all times
- •Performs any psychological examinations required
- •Participates in any meetings required by the sponsors
- •Ability to perform physical and neurological examinations
- •Ability to interpret laboratory results and ECG readings
- •Job Types: Part-time, Per diem
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