About the job
About Care Access
At Care Access, we are committed to enhancing global health by bridging gaps in healthcare access. With an extensive network of research sites, mobile clinics, and dedicated medical professionals worldwide, we deliver premier healthcare and research services to communities facing significant barriers to care. Our mission revolves around empowering individuals to take charge of their health and facilitating their involvement in pioneering medical research.
Through initiatives such as Future of Medicine, which provides advanced health screenings and research opportunities to global communities, and Difference Makers, which champions local leaders in their health and wellness endeavors, we prioritize people at the core of medical advancement. By leveraging partnerships, innovative technology, and tenacity, we are redefining how clinical research and health services are delivered, aiming for a healthier, more accessible future for everyone.
For more information about Care Access, please visit www. CareAccess.com.
Impact of Your Role
As a Sub Investigator, you will engage in both regional travel and remote telemedicine activities to support our clinical research studies. Your expertise in administering investigational products (IV, SC, TD, IM, PO administration), conducting physical examinations, and monitoring patient reactions to investigational products will be vital. We seek highly motivated Nurse Practitioners or Physician Assistants to facilitate clinical trial activities across various states in the USA.
Your Contributions
- Collaborate closely with the Principal Investigator to ensure the effective implementation of study protocols, assigning responsibilities to site staff as necessary and ensuring adherence to study protocols, laboratory procedures, Good Clinical Practice (GCP) standards, Standard Operating Procedures (SOPs), quality assurance (QA/QC) procedures, OSHA guidelines, and other applicable regulations.
- Participate actively in meetings with the director, other managers, and staff as required.
- Adhere to regulatory requirements, policies, procedures, and established standards of practice.
- Understand and review informed consent forms, protocols, and associated documentation.
