Advance Research Center LLC

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Doctors and Staff

INVESTIGATOR

Annia Cotorruelo Martinez, MD Doctor of Medicine, Internal Medicine Specialist.

Certified by the Florida Department of Health and has over 20 years of experience in the medical field. Dra Annia is on a mission to use his knowledge and experience to help the community, bringing them up-to-date information that impacts their health and keeping herself informed about the latest developments in drugs and treatments.

Principal researcher in charge of carrying out objective research that generates independent, high-quality and reproducible results. She is responsible for the management and integrity of the design, conduct and reporting of the research project and for managing, monitoring, and ensuring the integrity of any collaborative relationship. In addition, being responsible for directing and supervising the compliance, financial, personnel, and other related aspects of the research project and for coordination with school, department, and central administration personnel to ensure that the research is carried out. carried out by federal regulations. and policies and procedures of universities and sponsoring agencies.

Ricardo L. Perez, MD Doctor of Medicine, Internal Medicine Specialist.

He is a doctor focused on patient well-being with extensive experience in patient care, clinical diagnosis, management of other doctors, and care for chronic diseases.

Specialized research professional who works as Principal Investigator (PI) and Sub-investigator management. Evaluate the study proposal and decide on participation, facilitate/verify formal approvals by FDA and ICH GCP and local requirements, ensure that all site initiation activities are performed to initiate and conduct the study, and participate in the selection of trial subjects according to recruitment, strategy, performs and supervises the completion of procedures related to the study monitors the safety of trial subjects and research personnel, collects accurate and verifiable data, and the handling of the investigational product, with excellent communication with subjects, personnel from sponsors, and IEC/IRB, and ensure proper closure of the study

Manuel S. Mendizabal Gynecologist & Obstetric Specialist.

Specialized research professional who works as Director of the Principal Investigator (PI) and Sub investigator. Evaluate the study proposal and decide on participation, facilitate/verify formal approvals by FDA and ICH GCP and local requirements, ensure that all site initiation activities are performed to initiate and conduct the study, and participate in the selection of trial subjects according to recruitment. strategy, perform and supervise the performance of study-related procedures and monitor the safety of trial subjects and research personnel, collect accurate and verifiable data and handling of the investigational product, communicate with subjects, trial personnel sponsors and IEC/IRB, and ensure proper closure of the study. I am a diligent, patient-centered physician and medical director with extensive experience in patient care, diagnostics, clinical diagnosis, management of other physicians, and chronic disease and anti-disease care.

Francisco Martin Garrido Pediatric Specialist.

Dedicated Pediatrician with extensive experience in well and sick care of pediatric patients from newborn to 18+. Personable professional able to relate to a wide range of patients, parents, and staff. Motivational leader with a genuine love of kids and a desire to improve the health and wellbeing of every patient. Experienced preceptor dedicated to increasing students’ understanding and appreciation of the art of general medicine and to help them gain familiarity with the health issues facing the pediatric population with specialty in underserved communities.

Specialized research professional working as Principal Investigator,evaluate the study proposal and decide on participation, facilitate/verify formal approvals according to FDA and ICH GCP and local requirements, ensure that all site initiation activities are performed to start and conduct the study, participate in the selection of trial subjects according to the recruitment strategy, perform and supervise the conduct of study-related procedures and monitors the safety of the trial subjects and investigational staff, collect accurate and verifiable data and the handling of the investigational product, communicates with subjects, sponsors personnel, and IEC/IRB, and ensure adequate close-out of the study.

Rafael Cartaya, MD General Medicine.

Is a Board Medical Doctor with experience FDA-regulated clinical trials of research and clinical experience in the US, working in ER, ICU and CCU, Home Health and Hospice, competent performing invasive procedures. Working as a PCP for several nursing facilities in the Miami -Dade and Broward County area, also providing care for Home Bound residents in the Community.

Is responsible for the management and integrity of the design, conduct, and reporting of the research project and for managing, monitoring, and ensuring the integrity of any collaborative relationships.

SUB-INVESTIGATOR

Baliunis Ortega, FMG, FNP, RN, BSN.

Foreign Physician professional with twelve years’ experience in the health industry, Board Certified FNP is involved in research and participated in several clinical trials. More than 3 years of experience in clinical trials. Background in General Practitioner and first surgical assistant, Family Practice Specialist, Orthopedic and traumatology specialist.

Excellent communication skills and proven patient’s satisfaction record. Team player with diligent work habits. Bilingual in English and Spanish. Foreign Doctor in Medicine with 20 years of experience in the Medical Field.

Sandra De la Rosa FMG, FNP, RN, BSN.

Foreign Physician professional with 6 years in the research field and 10 years of experience in the health industry. Background in General Practitioner, Family Practice Specialist Excellent communication skills and proven patient satisfaction record. Team player with diligent work habits. Bilingual in English and Spanish. Reliable Register Nurse with excellent client care, and clinical experience, work well with bedridden, physically, and mentally challenged and memory impaired clients.

Friendly and compassionate, with excellent interpersonal communication skills. Specialized research professional working with and under the direction of the principal investigator (PI). While the Principal Investigator is primarily responsible for the overall design, conduct, and management of the clinical trial, the CRC supports, Facilities, and coordinates the daily clinical trial activities and plays a critical role in the conduct of the study.

Ruben Valderrama, FMG, APRN, MSN, FNP-C.

Solution-oriented nurse practitioner providing patient-centered care Specialized research professional 4 years working with and under the direction of the Principal Investigator (PI) with exceptional results, as a Sub-Investigator supports, sets up, and coordinates the daily activities of the clinical trial and plays a fundamental role in conducting the study.

Foreign Doctor in Medicine with 20 years of experience in the Medical Field. Excellent communicator who engages patients. Performs and supervises study-related procedures and monitors the safety of trial subjects and research personnel, collects accurate and verifiable data and handling of the investigational product, with excellent communication with subjects, sponsors’ personnel and IEC/IRB, and ensures proper closure of the study.

NURSE COORDINATOR

Yanet Molina, FMG, BSN, CRC.

Reliable Register Nurse with excellent client care, is involved in research and participated in several clinical trials. More than 6 years of experience in clinical trials and clinical experience, work well with bedridden, physically, and mentally challenged and memory impaired clients. Friendly and compassionate, with excellent interpersonal communication skills. Attention to detail, dutiful respect for compliance in all regulated environments, as well as supervisory skills including hiring, termination, scheduling, training, payroll, billing and other administrative tasks. Foreign Doctor in Medicine WITH  16 years of experience in the Medical Field.

Lazaro Roque, FMG, ASN, CRC.

Reliable Register Nurse with excellent client care, specialized research professional since 2016 working with and under the direction of the principal investigator (PI) and Sub-Investigators. Management of the clinical trial, the CRC supports, Facilities and coordinates the daily clinical trial activities and plays a critical role in the conduct of the study. By performing these duties, the CRC works with the PI, department, sponsor, and institution to support and provide guidance on the administration of the compliance, finance, personnel, and other related aspects of the clinical study. Foreign Doctor in Medicine WITH    16 years of experience in the Medical Field.

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