Clinical Research Nurse Practitioner - Sub Investigator
Behavioral Health Market Context
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Benefits
Health Insurance
Job Description
ctor and clinical research staff to ensure the safe and effective execution of protocols. This is a full-time, permanent opportunity for an NP with experience in clinical research who is passionate about advancing medical innovation while providing high-quality patient care.
Key Responsibilities
• Serve as a Sub-Investigator (Sub-I) on clinical trials under the supervision of the Principal Investigator/Medical Director.
• Perform delegated medical assessments and procedures in strict accordance with study protocols.
• Conduct and document study-related assessments, including physical exams, medical history reviews, and safety evaluations.
• Collaborate with study coordinators and other research staff to ensure protocol compliance, accurate data collection, and patient safety.
• Evaluate and manage adverse events, ensuring proper reporting and follow-up per regulatory and sponsor requirements.
• Maintain current knowledge of study protocols, informed consent processes, and GCP/ICH guidelines.
• Participate in study initiation, monitoring, and close-out visits as required.
• Perform additional duties as delegated by the Medical Director.
Qualifications
• Nurse Practitioner (NP) licensure in the state of Colorado (active and unrestricted).
• Minimum 1 year of full-time clinical research experience (required).
• Experience as a Sub-Investigator or in direct clinical trial involvement preferred.
• Strong knowledge of GCP, ICH guidelines, and FDA regulations.
• Excellent clinical judgment and ability to make sound medical decisions within scope of practice.
• Strong organizational, communication, and interpersonal skills with the ability to work collaboratively in a multidisciplinary research environment.
Compensation & Benefits
• Competitive salary (commensurate with experience).
• Full-time, permanent placement with benefits (details provided upon discussion).
• Opportunity to work with an experienced research team advancing innovative therapies.
Working Hours: Monday - Friday: 8 AM - 5 PM
Key Responsibilities
• Serve as a Sub-Investigator (Sub-I) on clinical trials under the supervision of the Principal Investigator/Medical Director.
• Perform delegated medical assessments and procedures in strict accordance with study protocols.
• Conduct and document study-related assessments, including physical exams, medical history reviews, and safety evaluations.
• Collaborate with study coordinators and other research staff to ensure protocol compliance, accurate data collection, and patient safety.
• Evaluate and manage adverse events, ensuring proper reporting and follow-up per regulatory and sponsor requirements.
• Maintain current knowledge of study protocols, informed consent processes, and GCP/ICH guidelines.
• Participate in study initiation, monitoring, and close-out visits as required.
• Perform additional duties as delegated by the Medical Director.
Qualifications
• Nurse Practitioner (NP) licensure in the state of Colorado (active and unrestricted).
• Minimum 1 year of full-time clinical research experience (required).
• Experience as a Sub-Investigator or in direct clinical trial involvement preferred.
• Strong knowledge of GCP, ICH guidelines, and FDA regulations.
• Excellent clinical judgment and ability to make sound medical decisions within scope of practice.
• Strong organizational, communication, and interpersonal skills with the ability to work collaboratively in a multidisciplinary research environment.
Compensation & Benefits
• Competitive salary (commensurate with experience).
• Full-time, permanent placement with benefits (details provided upon discussion).
• Opportunity to work with an experienced research team advancing innovative therapies.
Working Hours: Monday - Friday: 8 AM - 5 PM
Qualifications
- •Nurse Practitioner (NP) licensure in the state of Colorado (active and unrestricted)
- •Minimum 1 year of full-time clinical research experience (required)
- •Strong knowledge of GCP, ICH guidelines, and FDA regulations
- •Excellent clinical judgment and ability to make sound medical decisions within scope of practice
- •Strong organizational, communication, and interpersonal skills with the ability to work collaboratively in a multidisciplinary research environment
Benefits
- •Compensation & Benefits
- •Competitive salary (commensurate with experience)
- •Full-time, permanent placement with benefits (details provided upon discussion)
- •Opportunity to work with an experienced research team advancing innovative therapies
Responsibilities
- •The NP will serve as a Sub-Investigator on clinical trials, working closely with the Medical Director and clinical research staff to ensure the safe and effective execution of protocols
- •This is a full-time, permanent opportunity for an NP with experience in clinical research who is passionate about advancing medical innovation while providing high-quality patient care
- •Serve as a Sub-Investigator (Sub-I) on clinical trials under the supervision of the Principal Investigator/Medical Director
- •Perform delegated medical assessments and procedures in strict accordance with study protocols
- •Conduct and document study-related assessments, including physical exams, medical history reviews, and safety evaluations
- •Collaborate with study coordinators and other research staff to ensure protocol compliance, accurate data collection, and patient safety
- •Evaluate and manage adverse events, ensuring proper reporting and follow-up per regulatory and sponsor requirements
- •Maintain current knowledge of study protocols, informed consent processes, and GCP/ICH guidelines
- •Participate in study initiation, monitoring, and close-out visits as required
- •Perform additional duties as delegated by the Medical Director
- •Working Hours: Monday - Friday: 8 AM - 5 PM
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