About Care Access
Care Access is working to make the future of health better for all. With hundreds of research locations, mobile clinics, and clinicians across the globe, we bring world-class research and health services directly to communities that often face barriers to care. We are dedicated to ensuring that every person has the opportunity to understand their health, access the care they need, and contribute to the medical breakthroughs of tomorrow.
With programs like Future of Medicine , which makes advanced health screenings and research opportunities accessible to communities worldwide, and Difference Makers , which supports local leaders to expand their community health and wellbeing efforts, we put people at the heart of medical progress. Through partnerships, technology, and perseverance, we are reimagining how clinical research and health services reach the world. Together, we are building a future of health that is better and more accessible for all.
To learn more about Care Access, visit www.CareAccess.com .
How This Role Makes a Difference
The Sub-Investigator will be responsible for travel mixed with remote tele-medicine work to support our clinical research studies. Additionally, our Sub-Investigator will be skilled in administering investigational products (IV, SC, TD, IM, PO administration), performing physical examinations, monitoring for investigational product related reactions, among other duties beyond the standard clinical research Sub-Investigator role. Care Access is looking for highly motivated Nurse Practitioners or Physician’s Assistants to support clinical trial related activities in states throughout the USA.
How You'll Make An Impact
Clinical Research Patient Care & Study Procedures
Conduct study visits; perform physical exams; administer investigational products (oral, IV, IM, SQ, transdermal); perform phlebotomy, IV placement, vital signs, ECGs, specimen collection/processing; monitor participants throughout the study; educate participants on study medications; provide direct clinical care and maintain a safe clinical environment.
Protocol Compliance & Regulatory Oversight
Ensure compliance with study protocols, GCP, SOPs, IRB requirements, OSHA standards, and applicable regulations; review informed consent, protocol, and investigator brochure; complete and sign study documentation; oversee delegated study activities and ensure accurate documentation.
Medical Oversight & Safety Monitoring
Assess and manage adverse events and infusion reactions; review laboratory and clinical data for medical significance; provide medical management of study participants; evaluate eligibility, approve enrollment/randomization, and ensure timely reporting of serious adverse events to the Principal Investigator.
Study Coordination & Communication
Collaborate with the Principal Investigator and research team; communicate with study participants, sponsors, IRBs, and internal departments; attend meetings; support subject recruitment, prescreening, scheduling, and coordination of study activities.
Training, Leadership & Administrative Responsibilities
Train and mentor clinical staff on study procedures; delegate responsibilities appropriately; maintain clinical readiness; participate in quality improvement activities; complete required documentation and perform other assigned duties.
The Expertise Required
Ability to check, perform, and document vitals as well as EKG (ECG)
Phlebotomy and expert IV skills
Excellent working knowledge of medical and research terminology
Excellent working knowledge of federal regulations, good clinical practices (GCP)
Ability to communicate and work effectively with a diverse team of professionals.
Strong organizational skills: Able to prioritize, support, and follow through on assignments with good understanding of medical terminology.
Communication Skills: Strong verbal and written communication skills as evidenced by positive interactions with coworkers, management, clients and…