About Us

Welcome to Life Medical Research Group, where we are dedicated to advancing medical science and improving patient care through innovative clinical research. Our mission is to conduct high-quality studies that contribute to the development of new treatments and enhance healthcare outcomes.

Our Mission

Our mission is to drive medical progress by conducting rigorous and ethical clinical research. We aim to provide valuable insights that lead to new therapies, improve patient outcomes, and enhance the overall quality of healthcare.

Our Values

  • Integrity: We uphold the highest standards of honesty and transparency in all our research activities, ensuring that our studies are conducted with the utmost ethical considerations.
  • Excellence: We are committed to excellence in every aspect of our work, from study design and execution to data management and participant care.
  • Innovation: We embrace innovation and continuously seek out new methodologies and technologies to enhance the quality and efficiency of our research.
  • Collaboration: We value collaboration with pharmaceutical sponsors, CROs, and healthcare professionals to achieve common goals and drive research success.
  • Patient-Centricity: We prioritize the well-being and comfort of our participants, ensuring that their experience is positive and their needs are met throughout the study.

Why Choose Us

If you have questions, suggestions or want to be part of our research, we invite you to join us and together we take a leap towards the future of medicine at the local level.

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Our Team

At Life Medical Research Group Corp, our team of highly qualified and experienced professionals is dedicated to advancing clinical research at the site level. Our diverse group works collaboratively to ensure the successful execution of clinical trials, providing exceptional care and support to all participants.

  • Clinical Research Coordinators: Our clinical research coordinators manage the day-to-day operations of clinical trials at our site. They oversee participant recruitment, informed consent processes, data collection, and ensure compliance with study protocols. Their hands-on approach ensures that each study runs smoothly and efficiently.
  • Healthcare Professionals: Our skilled clinicians and nurses provide exceptional care to participants, conducting physical exams, administering study treatments, and monitoring patient health throughout the trial. Their expertise ensures participants’ safety and well-being.
  • Pharmacy Staff: Our pharmacy staff is responsible for the accurate dispensing and management of study medications. They ensure that all medications are stored, handled, and administered according to protocol, maintaining the highest standards of safety and compliance.
  • Laboratory Staff: Our laboratory technicians manage the processing and storage of biological samples. They support the integrity of our research data through meticulous attention to detail and adherence to strict quality control measures.
  • Regulatory Specialists: Our regulatory staff ensures that all clinical trials adhere to local, national, and international regulations. They manage submissions to regulatory authorities, maintain compliance with Good Clinical Practice (GCP) guidelines, and ensure all necessary approvals are obtained for each study.
  • Administrative Staff: Our efficient administrative staff handle the logistical and operational aspects of the research process. They manage documentation, coordinate schedules, and facilitate communication between departments, ensuring seamless site operations.
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Our Facility

We are equipped with state-of-the-art facilities, including modern exam rooms, a fully equipped pharmacy, and advanced laboratory services. Our facilities are designed to support a wide range of clinical trials and provide a safe, comfortable environment for participants.

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Our Achievements

  • Successful Studies: We have conducted numerous successful studies across various therapeutic areas, contributing to the development of new treatments and therapies.
  • Certifications and Accreditations: Our site is accredited by leading regulatory bodies and adheres to Good Clinical Practice (GCP) and other industry standards.
  • Positive Impact: Our research has led to significant advancements in medical science and improved patient care outcomes.

Expert Doctors.
Professional Care.

Dr. Sander Fernandez

Dr. Sander Fernandez

Family Medicine
Principal Investigator/ Sub Investigator

Dr. Fernandez is a Board-Certified Family Medicine Physician, who specializes in Clinical Trials Research, Regenerative Medicine, Sport Medicine, Non-Surgical Pain Management, and Men’s Health.

 

Dr. Luis Arias

Dr. Luis Arias

Internal Medicine – Rheumatology
Principal Investigator/ Sub Investigator

Dr. Arias is Board-Certified in Internal Medicine and Rheumatology, he specializes in Rheumatologic conditions diagnosis and treatment and Clinical Research. 

 

Dr. Margarita Perez

Dr. Margarita Perez

Internal Medicine – Cardiologist
Principal Investigator/ Sub Investigator

Dr. Perez is Board-Certified in Internal Medicine, Cardiovascular Diseases, Heart Failure and Echocardiography, she specializes in Cardiovascular Care and Clinical Research.

 

Dr. Ana Apaza

Dr. Ana Apaza

Internal Medicine – Endocrinologist
Principal Investigator/ Sub Investigator

Dr. Apaza is Board-Certified in Internal Medicine and Endocrinology, she specializes in treating Endocrine Disorders and Clinical Research.

 

NATIVE3:

NASH Trial

 

We are currently enrolling participants aged 18 and older for a Phase III clinical trial focused on Nonalcoholic Steatohepatitis (NASH). This study aims to evaluate the safety and effectiveness of an investigational treatment for individuals diagnosed with NASH. Qualified participants will receive study-related care and monitoring from experienced medical professionals at no cost.

 

 

SYNCHRONY HISTOLOGY:

NASH/ MASH Trial

 

We are currently enrolling participants from 18 to 80 years old for a Phase III clinical trial focused on Nonalcoholic Steatohepatitis (NASH/MASH). This study aims to evaluate the safety and effectiveness of an investigational treatment for individuals diagnosed with NASH. Qualified participants will receive study-related care and monitoring from experienced medical professionals at no cost.

 

 

SYNCHRONY OUTCOMES:

Compensated Cirrhosis due to NASH/ MASH Trial

 

We are currently enrolling participants from 18 to 80 years old for a Phase III clinical trial focused on compensated cirrhosis due to Nonalcoholic Steatohepatitis (NASH/MASH). This study aims to evaluate the safety and effectiveness of an investigational treatment for individuals diagnosed with NASH and compensated cirrhosis. Qualified participants will receive study-related care and monitoring from experienced medical professionals at no cost.

 

 

Sjögren's Syndrome Trial

 

We are currently enrolling female participants from 18 to 75 years old for a Phase II clinical trial focused on Sjögren's syndrome. This study aims at improving moderate to severe symptoms of fatigue, dryness and/or pain related to this disease. Qualified participants will receive study-related care and monitoring from experienced medical professionals at no cost.