Sub-Investigator / Nurse Practitioner
BioTalent · Miami, Florida, United States
FULL TIMEpermanent
Job Description
Sub-Investigator/ Nurse Practitioner Miami, FL | On-site Full-Time
If you are interested in applying for this job, please make sure you meet the following requirements as listed below.
Help Advance Life-Changing Clinical Research Great opportunity for Nurse Practitioners interested in clinical research and patient-focused studiesAre you passionate about clinical research, patient care, and advancing innovative therapies? We're looking for a Sub-Investigator to join a growing clinical research team supporting Phase I-IV studies across a variety of therapeutic areas, including neuroscience, psychiatry, neurology, acute pain, and metabolic disorders.If you thrive in a fast-paced clinical environment and want to contribute to cutting-edge research that helps bring new therapies to patients, this could be your next opportunity.
What You'll Do Serve as the medical provider supporting the Principal Investigator in the oversight of clinical trials Conduct study visits, medical evaluations, and ongoing assessments for research participants Ensure compliance with study protocols, GCP, ICH guidelines, and regulatory requirements Monitor participant safety, evaluate adverse events, and provide appropriate medical care when needed Lead and oversee the informed consent process to protect participant rights and welfare Collaborate with sponsors, study monitors, IRBs, physicians, and research staff throughout the study lifecycle Review and maintain accurate clinical documentation, source records, and study-related data Support patient recruitment, study enrollment, site operations, audits, and overall trial execution from a clinical and regulatory perspective
What We're Looking For Nurse Practitioner (NP) license required Experience as a Sub-Investigator in industry-sponsored clinical trials preferred Understanding of Good Clinical Practice (GCP), International Council for Harmonisation (ICH) guidelines, and regulatory requirements
Skills and knowledge in:Clinical ResearchMedical TerminologyPatient CareGCP ComplianceICH GuidelinesInformed Consent ProcessRegulatory ComplianceIRB ProcessesSubject Recruitment and RetentionClinical DocumentationSponsor and Monitor InteractionsClinical OperationsCommunication and Presentation SkillsNegotiation and Relationship BuildingMicrosoft Office (Word, Excel) and Clinical Research Systems
CompensationBase Salary: $100,000 - $150,000 annually, depending on experience and qualifications. xzbcwsv Additional compensation and benefits package available
Please Note On-site in Miami, FL Full-time clinical research position Opportunity to support Phase I-IV clinical trials Ability to travel overnight as needed Must maintain an active NP license No relocation assistance mentioned No visa sponsorship information providedIf this sounds like you, or someone in your network, I'd love to connect!#ClinicalResearch #NursePractitioner #SubInvestigator #ClinicalTrials #GCP #ICH #HealthcareCareers #ResearchJobs #LifeSciences #Hiring #RogersAR
If you are interested in applying for this job, please make sure you meet the following requirements as listed below.
Help Advance Life-Changing Clinical Research Great opportunity for Nurse Practitioners interested in clinical research and patient-focused studiesAre you passionate about clinical research, patient care, and advancing innovative therapies? We're looking for a Sub-Investigator to join a growing clinical research team supporting Phase I-IV studies across a variety of therapeutic areas, including neuroscience, psychiatry, neurology, acute pain, and metabolic disorders.If you thrive in a fast-paced clinical environment and want to contribute to cutting-edge research that helps bring new therapies to patients, this could be your next opportunity.
What You'll Do Serve as the medical provider supporting the Principal Investigator in the oversight of clinical trials Conduct study visits, medical evaluations, and ongoing assessments for research participants Ensure compliance with study protocols, GCP, ICH guidelines, and regulatory requirements Monitor participant safety, evaluate adverse events, and provide appropriate medical care when needed Lead and oversee the informed consent process to protect participant rights and welfare Collaborate with sponsors, study monitors, IRBs, physicians, and research staff throughout the study lifecycle Review and maintain accurate clinical documentation, source records, and study-related data Support patient recruitment, study enrollment, site operations, audits, and overall trial execution from a clinical and regulatory perspective
What We're Looking For Nurse Practitioner (NP) license required Experience as a Sub-Investigator in industry-sponsored clinical trials preferred Understanding of Good Clinical Practice (GCP), International Council for Harmonisation (ICH) guidelines, and regulatory requirements
Skills and knowledge in:Clinical ResearchMedical TerminologyPatient CareGCP ComplianceICH GuidelinesInformed Consent ProcessRegulatory ComplianceIRB ProcessesSubject Recruitment and RetentionClinical DocumentationSponsor and Monitor InteractionsClinical OperationsCommunication and Presentation SkillsNegotiation and Relationship BuildingMicrosoft Office (Word, Excel) and Clinical Research Systems
CompensationBase Salary: $100,000 - $150,000 annually, depending on experience and qualifications. xzbcwsv Additional compensation and benefits package available
Please Note On-site in Miami, FL Full-time clinical research position Opportunity to support Phase I-IV clinical trials Ability to travel overnight as needed Must maintain an active NP license No relocation assistance mentioned No visa sponsorship information providedIf this sounds like you, or someone in your network, I'd love to connect!#ClinicalResearch #NursePractitioner #SubInvestigator #ClinicalTrials #GCP #ICH #HealthcareCareers #ResearchJobs #LifeSciences #Hiring #RogersAR
Details
| Company | BioTalent |
| Location | Miami, Florida, United States |
| Type | FULL TIME |
| Niche | hr |
| Experience | permanent |