Sub-Investigator

About Care Access Care Access is working to make the future of health better for all. We bring world‑class research and health services directly into communities that often face barriers to care. Through programs such as Future of Medicine and Difference Makers, we reimagine how clinical research and health services reach the world. To learn more, visit

The Sub‑Investigator will be responsible for regional travel mixed with remote tele‑medicine work to support clinical research studies. The role involves administering investigational products (IV, SC, TD, IM, PO), performing physical examinations, monitoring for investigational product‑related reactions, and other duties beyond the standard Sub‑Investigator role. Care Access seeks highly motivated Nurse Practitioners or Physician Assistants to support clinical trial activities across the USA.

• Work closely with the Principal Investigator to oversee study protocols, delegating duties to site staff and ensuring compliance with GCP, SOPs, QA/QC, OSHA guidelines, and state/local regulations.
• Attend and participate in meetings with directors, managers, and staff as necessary.
• Comply with regulatory requirements, policies, procedures, and standards of practice.
• Read and understand the informed consent form, protocol, and investigator's brochure.
• Be available to see subjects virtually or in person as dictated by project design, answer their questions, and resolve medical issues during study visits.
• Sign and ensure that study documentation for each visit is completed.
• Perform all study responsibilities in compliance with the IRB‑approved protocol.
• Administer investigational products via subcutaneous, transdermal, intramuscular, intravenous, or oral routes.
• Proficiency in starting, monitoring, and maintaining intravenous lines.
• Proficiency in phlebotomy, proper blood collection practices, and laboratory processing (can be learned).
• Contribute as an active member of clinicians involved in managing infusion or other investigational product‑related reactions.
• Maintain a clean, efficient clinical area to assure highest standards of patient care.
• Follow safety and PPE procedures and maintain documentation of infusion procedures.
• Provide timely communication with internal teams, investigators, review boards, and study subjects.
• Prescreen study candidates by telephone and review exclusionary conditions or medications prior to scheduling screening appointments.
• Obtain informed consent per SOP.
• Administer delegated study questionnaires, as appropriate.
• Collect and evaluate medical records.
• Complete visit procedures and ensure proper specimen collection, processing, and shipment in accordance with protocol.
• Train others and complete basic clinical procedures (blood draws, vital signs, ECGs, etc.).
• Review screening documentation and approve subjects for admission to study.
• Review admission documentation and approve subject for randomization.
• Provide ongoing assessment of the study subject/patient to identify adverse events.
• Ensure serious and unexpected adverse events are reported promptly.
• Review and evaluate all study data and comment on clinical significance of out‑of‑range results.
• Perform physical examinations as part of screening evaluation and active study conduct.
• Provide medical management of adverse events as appropriate.
• Dispense study medication per protocol and/or IVRS systems. Educate patients on proper administration and importance of compliance.
• Monitor patient progress on study medication.
• Other duties as assigned.

• Ability to check, perform, and document vitals and EKG (ECG).
• Phlebotomy and expert IV skills.
• Excellent working knowledge of medical and research terminology.
• Excellent working knowledge of federal regulations and good clinical practice (GCP).
• Effective communication and teamwork skills.
• Strong organizational skills and ability to prioritize and follow through.
• Strong verbal and written communication skills.
• Team collaboration skills and positive attitude.
• Strong computer skills with clinical trials database, IVR systems, electronic data capture, MS Word and Excel.
• Ability to balance tasks…