MplusM Consulting is a
boutique clinical research network

especializing in sites that cater to hispanic populations

60+ Clinical Research Sites
300+ Studies successfully run by our of Sites
200+ PIs in our Network

Who we are

We pride ourselves in being an asset to both sites and sponsors by facilitating all stages of the clinical trial process. We are their business development specialists that provide them with:

For sites we are their business development specialists that provide them with:

A constant flow of studies that match their capabilities and experience

Staff support and training

Redesign your brand

Patient recruitment and retention strategies

Budget and contract negotiation

Spanish Speaking Coordinators or Translation Services

For Sponsors and CROs we are a comprehensive service provider that:

Identify high performing sites in our network that best fill the requirements of the protocol.

Filter sites based on their quality metrics

Provide one budget one contract for several sites.

Ensure all documents, including Feasibilities and Contracts have a quick turnaround rate.

Serve as point of contact between sponsor and site.

Translation of study materials to Spanish and design patient education materials for Spanish populations

For sites

For sites we are their business development specialists that provide them with:

A constant flow of studies that match their capabilities and experience

Staff support and training

Redesign your brand

Patient recruitment and retention strategies

Budget and contract negotiation

Spanish Speaking Coordinators or Translation Services

For Sponsors and CROs

For Sponsors and CROs we are a comprehensive service provider that:

Identify high performing sites in our network that best fill the requirements of the protocol.

Filter sites based on their quality metrics

Provide one budget one contract for several sites.

Ensure all documents, including Feasibilities and Contracts have a quick turnaround rate.

Serve as point of contact between sponsor and site.

Translation of study materials to Spanish and design patient education materials for Spanish populations

Our mission as a company is to provide an excellent service to both of our clients: Sites and Sponsors by matching specific protocol requirements with the sites that can successfully perform them.

We strongly believe that quality must be at the forefront of the industry and that is why we act as quality gatekeepers, always aiming to work with the best-in-class research sites and Principal Investigators.

MplusM Consulting is strongly committed to increasing the participation of diverse patient populations in clinical research. We believe that as a whole, the industry needs to emphasize the inclusion of minorities in clinical research and we are committed to achieving this goal by working closely with our sites to engage with minority communities and encouraging their participation.

Our Network

Our sites are multi-therapeutic, with highly experienced PIs and many of them have been top enrollers for several studies.

Among the PIs and Sub-Is in our sites there are: Internists, General Practitioners, Cardiologists, Gastroenterologists, Urologists, Oncologists, Pediatricians, Psychiatrists, Neurologists, Orthopedists, Nephrologists, Psychologists, Rheumatologists, Ophthalmologists, Dermatologists, Infectious Disease Specialists, Endocrinologists, Obstetrician-Gynecologists, General Surgeons, Plastic Surgeons, Ophthalmologists, Oncologists, Hematologists, Radiologists, Pain Specialists and Podiatrists.

MplusM Consulting has a large site network that comprises 62 sites in the United States and Latin America.

Our sites

  • Are multi-therapeutic, with highly experienced PIs
  • Are high enrollers and quick starters (many have been top enrolling sites for studies)
  • All use central IRBs
  • Have vast research experience
  • PIs, CRCs and staff are all ICH/GCP certified
  • Have a minimum of three study coordinators
  • Use Central IRBs
  • Have dedicated regulatory document specialists
  • Have five day turnaround time for start up regulatory documents.
  • Have healthy volunteers and patient recruiters
  • Have large database of diverse patient populations (Special populations in Hispanics, Afro-Americans,
  • Whites and other ethnicities)
  • Have advanced life support certified nursing staff
  • Have remote data entry and quality control capabilities
  • Routinely train their investigator and coordinators

Experience by Therapeutic Area

For Sponsors/CROs

MplusM Consulting provides Sponsors and CROs the full range of services needed to achieve successful clinical trials. We match specific study protocol requirements with the sites that best fulfills them. Our ability to quickly identify the right sites, within our network, allows site identification, feasibility, and study startup to occur at an accelerated pace thus allowing Sponsors and CROs to save time and internal resources.

  • PI and Site identification
  • Feasibility process
  • Pre-qualification visits planning
  • CTA & Budget Negotiations
  • Patient Enrollment Support
  • Quality Oversight

The guiding principle of MplusM Consulting is to achieve excellence. For us excellence means quality, exceptional service, integrity and transparency. We are proud of the fact that our sites have never faced any disciplinary procedure and are consistently top patient recruiters in the United States.

We work in a highly flexible and adaptable manner to exceed the expectations of our Sponsors and CROs. For MplusM having satisfied customers is our top priority.

For Research Sites

How we work

Our business model is built around the premise of providing maximum value to our sites. We are a performance-based clinical research service; therefore, our main goal is for our sites to successfully perform as many clinical trials as possible and we work diligently to bring them a constant pipeline of studies.

To achieve our vision of excellence with our sites we are committed to providing them with:

A steady stream of studies that match their capabilities and experience

A large network that allows us to negotiate better budgets and contractual terms for our sites

Patient recruitment tools to help them achieve or surpass enrollment goals

Measurement tools and metrics to improve site performance

Budget and contract negotiation

Spanish Speaking Coordinators or Translation Services

Join our Network

We are continuously looking for experienced, high quality sites that share our vision of excellence to join our network.

Contact us to learn more about how to join our network

People

Our Team

Marta Nadal, PhD

CEO

Marta Nadal has held the position of CEO and Business Development Director at MplusM Consulting, LLC since 2009. Dr. Nadal holds a PhD degree in Clinical Psychology and has held several managing positions in clinics and hospitals both in the US and in Latin America.

During her tenure as CEO and Business Development Director at MplusM Consulting Dr. Nadal has concentrated in creating a solid network of quality research sites that offer outstanding clinical trial services. She prides herself in providing exceptional service to Sponsors and CROs and in working with them to accomplish successful clinical trials from study startup to completion. Dr. Nadal is very passionate about increasing Hispanic participation in clinical trials and has set that objective as a priority for the company.

Dr. Nadal is fluent in English, Spanish and Portuguese.

Marta Nelson

Director of operations

Marta Nelson is co-founder of MplusM Consulting, LLC and holds the position of Director of Operations. Marta is responsible for managing all the operations of our site network. She is also responsible for negotiating contracts and budgets and quality control.

Marta previously worked in health policy consulting, collaborating with large pharmaceutical companies in the development of new health care initiatives in the U.S. and Latin America.

Marta graduated from the London School of Economics with a Master of Science (MSc) degree. She is fluent in English and Spanish.

Randall Nelson, MSc

Business Development Manager

Randall Nelson holds the position of Business Development Manager. Randall is responsible for growing the network and recruiting new quality sites.

Randall previously worked in the health franchise sector where he managed the expansion and operations of major U.S. and European franchises in both Europe and in Latin America.

Randall holds a Master of Science degree from the University of London. He is fluent in English and Spanish.

Alfredo Ortiz

Regional Manager

Alfredo Ortiz is our Regional Manager for Mexico. He is responsible for the development of our site network in Mexico and for liaising with our sites in the country for all operational needs.

Previously Alfredo worked in the banking, financial sector and export related industries. He has in depth knowledge of the Mexican financial sector.

Alfredo holds a Bachelor of Science degree from the Instituto Tecnologico Autonomo de Mexico (ITAM).

News

The Effect of COVID-19 on Clinical Research Sites

COVID-19 has affected all of us; our daily routines have changed, social interactions have been limited, and businesses have suffered. With a network of over sixty clinical research sites in the United States, Mexico, and Honduras, we would like to share how the clinical research industry is faring from the sites’ perspective. Patient Enrollment During […] READ MORE

Why is minority inclusion in clinical trials necessary?

At MplusM Consulting we pride ourselves in being a network of clinical research centers focused largely on the hispanic and minority markets. We aim to increase the participation of minorities in clinical trials by working with minority physicians who can connect culturally and linguistlically to those hard to reach populations. However, we are concerned that […] READ MORE

Contact

Contact info

2940 Louise Street
Miami, Florida 33133
Tel: +-001 305 298 3179

Contact info

2940 Louise Street
Miami, Florida 33133
Tel: +-001 305 298 3179