Sub-Investigator

Sub-Investigator – Care Access – Tyler, TX

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 into 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.

Through programs such as Future of Medicine and Difference Makers, we put people at the heart of medical progress and reimagine how clinical research and health services reach the world.

The Sub-Investigator will perform regional travel mixed with remote tele‑medicine work to support our clinical research studies. Responsibilities include administering investigational products, performing physical examinations, monitoring for product‑related reactions, and all standard duties of a clinical research Sub‑Investigator. We seek highly motivated Nurse Practitioners or Physician Assistants to support clinical trials across the USA.

• Work closely with the Principal Investigator to oversee execution of study protocols, delegating duties to site staff, and ensuring site compliance with protocols, SOPs, GCP, QA/QC, OSHA guidelines, and state/local regulations.
• Attend and participate in meetings with the director, other 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 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.
• Initiate, monitor, and maintain intravenous lines.
• Perform phlebotomy, proper blood collection practices, and laboratory processing practices.
• Contribute actively to management of infusion or other investigational product related reactions.
• Maintain a clean, efficient clinical area to assure the highest standards of patient care.
• Follow safety and PPE procedures and maintain proper documentation of infusion procedures.
• Communicate timely with internal teams, investigators, review boards, and study subjects.
• Prescreen study candidates by telephone and review exclusionary conditions or medications prior to scheduling.
• 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 such as 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 that serious and unexpected adverse events are reported promptly to the investigator.
• Review and evaluate all study data and comment on the clinical significance of any 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 vitals and perform EKG.
• Phlebotomy and expert IV skills.
• Excellent working knowledge of medical and research terminology.
• Excellent working knowledge of federal regulations and GCP.
• Effective communication and teamwork with diverse professionals.
• Strong organizational and prioritization skills.
• Strong verbal and…