Nurse Practitioner Sub-Investigator: Clinical Research Lead

Iterative Health; New Albany (IN); Vor Ort; USD 90.000 - 135.000; Vollzeit

Zusammenfassung

Iterative Health seeks a licensed Nurse Practitioner to serve as a Sub Investigator across multiple active studies, combining advanced clinical practice with clinical research under the PI's supervision. You will support safety, eligibility, and protocol adherence while mentoring CRCs and staff.

You will perform histories and exams, contribute to informed consent discussions where delegated, manage adverse events, and maintain meticulous documentation in EMR/EDC, ensuring regulatory compliance

Qualifikationen

• Active, unrestricted Nurse Practitioner license in the applicable state.
• Minimum 3 years of clinical research experience preferred.
• Cardiovascular experience or willingness to develop expertise.
• Strong written and verbal communication skills; highly organized.

Aufgaben

• Serve as a delegated Sub-Investigator on clinical studies under the PI.
• Conduct medical histories and protocol-required physical examinations.
• Evaluate eligibility based on inclusion/exclusion criteria.
• Obtain informed consent when delegated by the PI.
• Monitor participant safety and report adverse events as needed.
• Order, review, interpret, and sign protocol-required assessments and results.
• Prescribe study-related medications per protocol and state law.
• Maintain accurate documentation in EMR/EDC systems; ensure GCP compliance.
• Ensure adherence to FDA/ICH-GCP/HIPAA and sponsor requirements.

Kenntnisse

Nurse Practitioner license

Clinical research

Cardiovascular experience

Communication skills

Organizational skills

Problem-solving

Physical stamina

Ausbildung

Nurse Practitioner license (unrestricted)

DEA registration preferred

Tools

EMR systems

EDC platforms

Office software

Jobbeschreibung

Iterative Health seeks a licensed Nurse Practitioner to serve as a Sub Investigator across multiple active studies, combining advanced clinical practice with clinical research under the PI's supervision. You will support safety, eligibility, and protocol adherence while mentoring CRCs and staff.

You will perform histories and exams, contribute to informed consent discussions where delegated, manage adverse events, and maintain meticulous documentation in EMR/EDC, ensuring regulatory compliance