Sub-Investigator (Nurse Practitioner)

As a Sub‑Investigator (Nurse Practitioner) you will deliver high‑quality, patient‑centered care through mobile health clinics, occasional home health visits, and support our mission to enhance the quality of life of our clients. Your responsibilities include: Ensuring participant safety, data integrity, and maintenance of protocol standards across therapeutic areas. Assisting virtual Principal Investigators (vPIs) with conducting clinical trials following federal, state, and institutional guidelines. Supporting fleet operations with daily unit maintenance, temperature monitoring, and inventory management. Co‑managing clinical trials from pre‑study implementation to study closure. Administering medications, investigational products, and vaccinations as delegated. Assessing serious and adverse events related to investigational products. Performing phlebotomy, IVs, subcutaneous injections, vital signs, ECG, and urine collection. Conducting participant visits (pediatric, adult, geriatric) including medical history, medication reconciliation, physical exam, and health education. Managing electronic data entry and ensuring timely data resolution. Coordinating recruitment, subject eligibility screens, and community outreach engagement. Providing leadership, mentorship, training, and protocol communication to study teams. Maintaining compliance with GCP, ICH guidelines, SOPs, and regulatory requirements. Supporting community outreach and recruitment strategies in diverse cultures. Performing other duties such as home visits, after‑hours, and weekend work as needed. Qualifications Education: Advanced practice degree (NP or PA). Experience: A minimum of two (2) years as an advanced practitioner and at least one (1) year of recent clinical research experience (preferred). Computer Skills: Excellent proficiency with Microsoft Outlook, Word, Excel, and PowerPoint. Certificates & Licenses: Current unrestricted licensure to practice as an NP or PA in the state of assignment; current BLS certification; CITI, GCP, and IATA preferred. Knowledge, Skills & Abilities: Excellent verbal and written communication. Experience with collecting, processing, and shipping lab specimens. Judgment and critical thinking in application of procedures and policies. Knowledge of federal, state, and local research regulations. Patient‑centric focus with adaptability and flexibility. Initiative to improve productivity and quality. Strong attention to detail and effective relationships. Ability to manage time and projects to meet deadlines. Physical ability to sit, stand, bend, reach, lift up to 50 lbs, and travel regionally or nationally. Valid state driver’s license and automobile insurance coverage. Cellular phone, reliable transportation, and internet access. Essential Functions and Areas of Accountability Lead and train study teams in clinical trial conduct and protocol requirements. Screen and confirm subject eligibility in compliance with HIPAA. Serve as primary clinician for participant visits (medical history, medication reconciliation, physical exam, health education). Manage clinical trial execution per protocol, GCP, ICH, and SOPs. Coordinate start‑up, vendor management, recruitment, source development review, scheduling, training, documentation, visits, data entry, query resolution, adverse event reporting, new protocol amendments, and close‑out reporting. Administer investigational products, vaccinations, and assess related events. Plan and execute clinical duties (drug preparation, phlebotomy, ECG, lab processing) within scope. Coordinate consent processes and ensure inclusion/exclusion criteria. Assist with electronic data entry and protocol review with PIs and leadership. Maintain compliance with OSHA, HIPAA, and State Board of Nursing. Support community engagement and recruitment through events and collaboration with health professionals. Perform extra duties, including home visits, after‑hours, weekend work, and on‑call shifts. Other duties as assigned to advance PCM missions. Pay & Benefits Typical base pay range: USD $102,400 – $161,500 per year, dependent on location, role complexity, duties, and experience. Available Benefits: Medical, Dental, Vision, 401(k), Company‑Paid Short‑Term Disability, Flexible Spending Account (FSA), Health Savings Account (HSA), Paid Time Off, Voluntary Benefits. Professional Case Management is an Equal Opportunity Employer. PCM is committed to diversity and inclusivity. #J-18808-Ljbffr Act for Health, Inc