Sub-Investigator at Revival Research Institute, LLC Sherman, TX

ocols, oversee compliance with regulatory standards, and provide direct patient care within clinical trials. Additionally, this role requires proficiency in administering investigational products (IV, SC, TD, IM, PO), performing physical examinations, and managing investigational product-related reactions.

Key Responsibilities
• Collaborate with the Principal Investigator (PI) to oversee study execution, ensuring compliance with GCP, SOPs, QA/QC procedures, OSHA guidelines, and applicable regulations.
• Conduct and document informed consent discussions with study participants.
• Perform physical examinations and assess patients for study eligibility and ongoing participation.
• Administer investigational products via subcutaneous, transdermal, intramuscular, intravenous, or oral routes.
• Monitor and manage adverse events and investigational product-related reactions.
• Maintain proper documentation of study visits, including signing off on medical records and assessments.
• Conduct prescreening evaluations by reviewing medical history and exclusionary conditions before scheduling appointments.
• Perform and oversee clinical trial procedures such as blood draws, EKGs, vital signs, and laboratory sample collection and processing.
• Train study staff on protocol requirements, phlebotomy, IV placement, and proper specimen handling.
• Ensure timely communication with internal teams, study sponsors, IRBs, and study participants.
• Oversee compliance with IRB-approved protocols and ensure accurate reporting of serious and unexpected adverse events to the PI.
• Educate patients on study medication administration and ensure adherence to protocol requirements.

Qualifications & Experience
• Education : Master’s Degree in a healthcare-related field. Licensed Nurse Practitioner (NP) or Physician Assistant (PA) in good standing.
• Experience :
• 5+ years of clinical experience (preferably in research or infusion setting).
• At least 1 year of experience as a Sub-Investigator in a clinical research setting (preferred).
• Experience as a Clinical Research Coordinator is a plus.
• Certifications/Licenses :
• Valid medical license in one or more U.S. states.
• Additional research-related certifications (e.g., GCP, IATA) are a plus.

Skills & Competencies
• Strong understanding of clinical research regulations, GCP guidelines, and study protocols.
• Proficiency in IV placement, phlebotomy, and blood sample collection.
• Ability to monitor, manage, and document adverse events.
• Experience with electronic data capture (EDC) systems and clinical trial databases.
• Excellent organizational, communication, and critical-thinking skills.
• Ability to work independently and collaboratively in a fast-paced research environment.
• Comfortable traveling regionally with short notice.

Why Join Revival Research Institute?
At Revival Research Institute, we are dedicated to advancing clinical research and improving patient outcomes. We offer a collaborative work environment where professionals can contribute to meaningful research while expanding their clinical expertise. If you are passionate about clinical research and want to make a difference, we invite you to apply for this opportunity.