Nurse Practitioner NP Clinical Research SubInvestigator

Nurse Practitioner (NP) – Clinical Research Sub-InvestigatorPrime Clinical Research Location: On-SiteEmployment Type: Full-Time or Part-TimeDepartment: Clinical Research OperationsReports To: Principal Investigator and Medical DirectorPrime Clinical Research is seeking an experienced Nurse Practitioner (NP) Sub-Investigator to support the conduct of clinical trials at our investigative site. This role works closely with the Principal Investigator and clinical research team to provide protocol-driven medical oversight, participant safety management, and high-quality clinical documentation. Clinical research experience is preferred but experienced Nurse Practitioners interested in transitioning into clinical research are encouraged to apply.The NP Sub-Investigator plays an essential role in protecting participant safety while ensuring studies are conducted in accordance with study protocols, Good Clinical Practice (GCP), and applicable regulatory requirements. Responsibilities include participant eligibility assessments, informed consent participation, investigational product oversight, safety monitoring, and collaboration with study coordinators and sponsor teams.This position is ideal for a Nurse Practitioner who enjoys combining clinical care with medical research and contributing to the development of new therapies.What you will doClinical Trial Medical Oversight Conduct protocol-required medical evaluations including medical history review, targeted physical exams, and review of laboratory results, imaging, and ECGsSupport participant eligibility determinations and document clinical rationale for inclusion or exclusion decisionsCollaborate with the Principal Investigator on complex eligibility cases and clinical decision-making Informed Consent and Participant Engagement Participate in the informed consent process and ensure participants understand study procedures, risks, and alternativesSupport re-consent following protocol amendments when requiredEnsure participant rights, safety, and autonomy are maintained throughout the study Safety Monitoring and Adverse Event Management Detect, assess, and manage adverse events and serious adverse events in accordance with protocol and regulatory requirementsInitiate protocol-directed actions such as dose modifications, treatment holds, or discontinuations when necessaryProvide appropriate clinical follow-up and ensure accurate safety documentation Investigational Product and Medication Oversight Ensure investigational product prescribing, dosing, and administration follow protocol requirementsReview concomitant medications for potential interactions or protocol restrictionsRecognize and manage infusion or administration reactions in collaboration with the study team Documentation and Data Quality Maintain timely, accurate source documentation aligned with ALCOA+ documentation standardsEnsure clinical documentation supports Electronic Data Capture entries and regulatory requirementsCollaborate with Study Coordinators to resolve data discrepancies and ensure documentation accuracy Monitoring, Audits, and Compliance Participate in sponsor monitoring visits, audits, and regulatory inspections as requiredSupport corrective and preventive action activities when neededMaintain inspection readiness through high-quality documentation and adherence to site SOPs Team Collaboration and Leadership Work closely with Principal Investigators, Study Coordinators, research staff, and sponsor teamsSupport training and mentoring of research staff on clinical oversight and safety processesPromote patient-centered research practices and high standards of clinical care Required Qualifications Active Nurse Practitioner license in the practicing jurisdictionCurrent national NP certification such as AANP or ANCCClinical experience relevant to the therapeutic areas conducted at the site or ability to onboard quicklyKnowledge of clinical trial protocols and participant safety managementStrong documentation and clinical decision-making skillsCurrent BLS or ACLS certification, as required by the site Preferred Qualifications Previous experience as a Sub-Investigator in clinical researchKnowledge of ICH Good Clinical Practice (GCP) and human subjects protectionsExperience working with clinical research systems or Electronic Data Capture platformsExperience participating in sponsor monitoring visits or regulatory inspections Work Environment On-site clinical research environment supporting active clinical trialsCollaboration with investigators, clinical research coordinators, and sponsor teamsCombination of clinical assessments and documentation responsibilities Why Prime Clinical ResearchPrime Clinical Research partners with pharmaceutical companies, biotechnology organizations, and contract research organizations to conduct clinical trials that advance medical innovation and improve patient outcomes.Our research teams are committed to maintaining the highest standards of patient safety, regulatory compliance, and research integrity while expanding access to emerging therapies.Prime Clinical Research is an Equal Opportunity Employer.

Created: 2026-03-20