

Empowering Clinical Research with 20 Years of Expertise
Let's Succeed Together
OUR MISSION
RM Clinical Research Consultant is dedicated to providing professional, ethical, and relevant consultation to research sites. Our mission is to elevate research sites to a senior level by leveraging innovative science and fostering community engagement

OUR STATEMENT
At RM Clinical Research Consultant, we specialize in clinical trials phases I-IV. Our services include education and training, research protocol development, quality assurance, and regulatory affairs support. With over 20 years of experience, we aim to achieve brand awareness, education, lead generation, and thought leadership through our website. We are committed to providing our clients with capability, adaptability, and scalability.

OUR OBJECTIVES
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Brand awareness and education
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Brand building
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Lead generation
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Thought Leadership
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Relationship Building
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Content Engagement
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Conversion

ABOUT THE FOUNDER
Reina Breton de Malcom MD is the visionary founder and CEO of RM Clinical Research Consultant. With over two decades of experience, she is a respected leader in the field of clinical research.

SERVICES
Education and Training
We provide engaging educational workshops and seminars tailored for healthcare professionals, patients, and community groups. Topics cover essential aspects of clinical research, including informed consent, clinical trial participation, and research ethics.
​Regulatory Affairs Support
We guide you through regulatory requirements and submissions for clinical research studies. Our services include preparing regulatory documents, interacting with regulatory agencies, and ensuring compliance throughout the research process.
Research Protocol Development
Our experts collaborate with healthcare organizations, research institutions, and pharmaceutical companies to develop robust research protocols. We ensure alignment with ethical standards, regulatory requirements, and best practices in clinical research.
Employees Workshop to Certify Employees
We offer specialized workshops for certify employees, including Junior Coordinators, Coordinators, Senior Coordinators, Managers, and Project Managers involved in research trials. Topics cover Source Document management, Good Clinical Practice (GCP), Lab Supplies Chain, Log maintenance, Regulatory Documents, Data Submission, Serious Adverse Event (SAE) reporting, and FDA audit preparation.
Quality Assurance and Compliance
Our consulting services focus on maintaining compliance with regulatory standards, institutional policies, and industry guidelines. We conduct audits, develop quality management systems, and provide training on compliance matters.
Research Recruitment and Retention
We strategize to attract and retain participants for clinical trials. Our outreach efforts target diverse populations, and we create effective recruitment materials. Additionally, we implement retention strategies to minimize dropout rates.
Data Management and Analysis
Our support extends to data management and analysis. We design databases, develop data collection tools, clean data, and perform statistical analysis. Our expertise ensures accurate interpretation of research findings.