Hector M Torres Navarro, MD

Experience

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  Empowering With Health

  Jan 2021 - Dec 2021

  Clinical Research Coordinator I

  Discussed study protocols and consent potential subjects/participants, explained the trial and answered subject questions and concerns; as well as checked in with them regularly to monitor compliance with the study guidelines. Patient consultation, obtained vital signs, performed ECGs, phlebotomy, give an injection, administer IV medications, and set up intravenous lines. Dispensed study medication according to protocol. Entered Data into EDC and answer Queries per FDA guidelines. Administered questionnaires/diaries per protocol. Submitted subject reimbursement requests after each visit, maintenance and filed of all regulatory documents. Show less

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  Universidad de Guadalajara

  Aug 2021 - Jan 2022

  High School Teacher

  •Designed and implemented a curriculum incorporated practical sessions on CPR techniques, wound care procedures, and first aid interventions. •Conducted interactive workshops to demonstrate and practice CPR techniques, wound care protocols, and first aid procedures with hands-on experience, enhancing their confidence and readiness to respond in emergency situations.•Developed and administered regular evaluations (written assessments, practical demonstrations, and simulated emergency response scenarios). Show less

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  Centro de Investigacion Medica de Aguascalientes

  Jan 2022 - Jan 2024

  Clinical Research Coordinator II

  Discussed study protocols and consent of potential subjects/participants, explained the trial and answered subject questions and concerns; as well as checked in with them regularly to monitor compliance with the study guideline. Recruited subjects to the trial, providing written communication of their participation and gave document subject informed consent process. Collected, managed, and maintained all study-related paperwork and correspondence. Collected processed, and ship blood/urine specimens. Obtained vital signs, performed ECGs, phlebotomy, give an injection, administer IV medications, and set up intravenous lines. Scheduled meetings, monitor visits, procedures, trials and set up for them. Performed other duties. Involved in the next clinical trials phase IV: XL184-313, GO42784, D9311C00001, MK7902-002 and PANOVA-3 Show less

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  Urology San Antonio

  Apr 2024 - now

  Clinical Data Coordinator

  Under minimal supervision, is responsible for the collection, coordination, processing and quality control of clinical trial data. May assist with screening patients for research protocols. Maintains research protocol information, regulatory documents and other research files as applicable. Works in compliance with Urology San Antonio Research Department (USARD) Standard Operating Procedure (SOP), principles of Good Clinical Practice and all applicable federal, state, and local regulations.• Extrapolates data, completes case report forms, and ensures timely data submission in accordance with USARD SOP. • Actively prepares for and participates in monitoring and auditing activities. Assists in ensuring that all queries are resolved in a timely manner in accordance with USARD SOP and sponsor requirements. • Responsible for processing, filing and maintaining protocol regulatory documents. • May assist with screening patients for potential study enrollment. • Responsible for assisting with patient scheduling for procedures required to maintain protocol compliance. • Responsible for assisting with coordinating patient follow-up visits and timely data submission. • Responsible for assisting with collection and processing of specimens, imaging documents, or other items required for research purposes. • Responsible for ordering and maintaining research supplies. • Responsible for assisting in the investigational drug accountability process. • Maintains research records in a confidential manner according to practice policies, sponsor confidentiality agreements, HIPAA guidelines and any other applicable regulations. • May lead and mentor other data coordinators at the site/location • May be responsible for coordinating patient billing and research payout/payment tracking. Show less