Isaac Esparza
Medical Doctor
Summary
- Medical Doctor, passionate about clinical research since student, I've 3 years experience on surgical research but also I have participated on studies from other medical specialties such as psychiatry, internal medicine, bariatric surgery and epidemiology. I am proudly Mexican and I'm willing to expand my borders to grow and achieve my dreams.
- Focused Clinical Research Coordinator well-versed in study protocols, standard operating procedures and general trial oversight. Excellent problem-solving abilities with a detail-oriented nature. Ready to bring 3 years of related experience to a challenging new role.
- Knowledgeable Clinical Research Associate adept at recognizing clinical values and abstract data from source documents. Uses analytical skills to identify data or patient safety issues.
- Organized and dependable candidate successful at managing multiple priorities with a positive attitude.
Overview
3
3
years of professional experience
6
6
years of post-secondary education
Work History
Clinical Research Coordinator
Fengh Academy of Minimally Invasive Surgery, CCBEMBC
Tijuana
06.2021 - Current
- Screened patient records, databases and physician referrals to identify prospective candidates for research studies.
- Collected data and followed research protocols, operations manuals and case report form requirements.
- Collected, evaluated and modeled collected data.
- Worked with principal investigator and sponsors to facilitate daily trial activities and comply with research protocols.
- Managed team of employees, overseeing hiring, training and professional growth of employees.
- Exceeded goals through effective task prioritization and great work ethic.
- Used Microsoft Office and other software tools to create documents and other communications.
- Devoted special emphasis to punctuality and worked to maintain outstanding attendance record.
Senior Clinical Research Associate
Unidad de Investigación Biomédica 02 Centro Médico Nacional de Occidente
Guadalajara
08.2019 - 05.2021
- Implemented electronic data capturing systems to adhere with clinical research guidelines.
- Screened patient records, databases and physician referrals to identify prospective candidates for research studies.
- Collected data and followed research protocols, operations manuals and case report form requirements.
- Reviewed participant eligibility and consent documentation to help researchers achieve accurate and meaningful results.
- Communicated project status to Comisión Interinstitucional para la Formación de Recursos Humanos para la Salud ( CIFRHS ) management verbally and through technical documentation and presentations.
- Directed, guided and delegated tasks to teams and developed project schedules, resource requirements and timelines to maintain productivity on goals and objectives.
- Organized and maintained research study regulatory documents in site binder to maintain accuracy and integrity.
- Synthesized and utilized key information from proposals, technical reports and publications to achieve objectives.
- Worked with principal investigator and sponsors to facilitate daily trial activities and comply with research protocols.
- Participated on international clinical trials such as "SARS-CoV-2 vaccination modelling for safe surgery to save lives: data from an international prospective cohort study" , and "Timing of surgery following SARS-CoV-2 infection: an international prospective cohort study" , collaborating with University of Birmingham .
- Participated on national clinical trials such as "Anxiety and COVID-19: Coronavirus Anxiety Scale scores in medical and non-medical personnel in urban hospitals in Guadalajara. A cross-sectional survey study" , "The Benefit of Perineural Injection Treatment with Dextrose for Treatment of Chondromalacia Patella in Participants Receiving Home Physical Therapy: A Pilot Randomized Clinical Trial" , "Gender Differences in Postoperative Pain, Nausea and Vomiting After Elective Laparoscopic Cholecystectomy" and "Differences in Postoperative Pain, Nausea, and Vomiting After Elective Laparoscopic Cholecystectomy in Premenopausal and Postmenopausal Mexican Women" .
- Maintained compliance with protocols covering patient care and clinical trial operations.
- Collected, evaluated and modeled collected data.
- Followed informed consent processes and maintained records.
Education
M.D. - Medicine
Universidad De Guadalajara
Guadalajara, Mexico 08.2015 - 08.2021
Skills
Trial management
undefinedTimeline
Clinical Research Coordinator
Fengh Academy of Minimally Invasive Surgery, CCBEMBC
06.2021 - Current
Senior Clinical Research Associate
Unidad de Investigación Biomédica 02 Centro Médico Nacional de Occidente
08.2019 - 05.2021
M.D. - Medicine
Universidad De Guadalajara
08.2015 - 08.2021
Similar Profiles
Bethany TaylorBethany Taylor
Registered Nurse at Minimally Invasive Surgery HospitalRegistered Nurse at Minimally Invasive Surgery Hospital
Monique GreenMonique Green
Surgical Practice Nurse at North Queensland Minimally Invasive SurgerySurgical Practice Nurse at North Queensland Minimally Invasive Surgery
Jessica EsquivelJessica Esquivel
Junior Doctor at Minimally Invasive Thoracic Surgery Institute - Hospital Ángeles LomasJunior Doctor at Minimally Invasive Thoracic Surgery Institute - Hospital Ángeles Lomas