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Join our Network

JOIN OUR CLINICAL RESEARCH NETWORK

FOMAT is a place where people are proud to work, have the opportunity to develop their careers and are enabled to realize their full potential. We are a therapeutically focused site management organization with a high performance reputation for conducting global clinical development programs of the highest integrity. We are one of Latin America’s largest SMOs for Phase I – Phase IV Clinical Trials, in terms of sites & quality results. Our size and scope permit our employees to experience working in various countries and cultures on projects for top pharmaceutical companies, biotech startups, and everything in between.

Join our Clinical Research Network, meet benefits and requirements for both US and LatAm Networks and affiliate to our upcoming studies.

For US PIs and Sites

Benefits for Principal Investigator (PI)

First look at new drugs under investigation and the ability to offer an alternative treatment to your patients.
A smooth transition into the pharmaceutical industry with the aid of a trained and professional research staff.
Valuable experience and networking opportunities within the industry.
First hand experience and knowledge in Clinical Research. Compensations for your time and support.
Brand/Name recognition through DRS marketing.
A volume of guaranteed contracts and budgets.

Requirements for Principal Investigator (PI)

Practicing Medical License Current and updated CV with previous research experience.
A signed Confidentiality Disclosure Agreement with DRS and to ensure that there is complete secrecy and confidentiality in managing information from the clinical studies,s by all personnel in the facility.
Up to date and trained in both Good Clinical Practices (GCP) and with the National Institute of Health (NIH).*
Have a sufficient amount of time to dedicate to Research.
A willingness and eagerness to get involved in Clinical Research and grow as a research site.

*If you don't have any training in Clinical Research, DRS will help you get trained. Contact us for more information.

Benefits for Sites

A constant flow of leads from DRS and valuable networking opportunities. Appropriate compensation for each study enrolling.
The aid of trained and experienced research staff to help with all start up activities (Regulatory/paperwork, contracts and budgets, conferences/Investigator meetings, monitor coordination, etc).
A network with other research sites in your community through DRS partners.
Assistance from DRS partnered sites through referrals for increased enrollment on hard to enroll studies.
Provided connections to local laboratories and customers who are already contracted for the development and results of clinical studies, with DRS.
Training from dedicated DRS staff.

Requirements for Sites

Have a designated space for DRS coordinators for the development of clinical studies and a secure storage area for study information.
Provide the necessary resources for the study conduction.
Provide a price list for the basic services offered at your practice.
Allow access to a Hispanic patient database for recruitment and reviewing purposes for study enrollment.
Work exclusively with DRS as your only Site Management Organization (SMO).

For LatAm PIs and Sites

Benefits for Principal Investigator (PI)

First look at new drugs under investigation and the ability to offer an alternative treatment to your patients.
Medical Training for the upcoming studies.
Help obtaining Good Clinical Practices (GCP) or National Institute of Health (NIH) certificate.*
A smooth transition into the pharmaceutical industry with the aid of a trained and professional research staff.
Valuable experience and networking opportunities within the industry.
First hand experience and knowledge in Clinical Research.
Compensations for your time and support.
Brand/Name recognition through FOMAT Medical Research marketing.
A volume of guaranteed contracts and budgets.

Requirements for Principal Investigator (PI)

Practicing Medical License Current and updated CV.
A signed Confidentiality Disclosure Agreement with FOMAT Medical Research and to ensure that there is complete secrecy and confidentiality in managing information from the clinical studies, by all personnel in the facility.
Up to date and trained in both Good Clinical Practices (GCP) and with the National Institute of Health (NIH).*
Have a sufficient amount of time to dedicate to Research.
A willingness and eagerness to get involved in Clinical Research and grow as a research site.

*If you don't have any training in Clinical Research, FOMAT will train you. Contact us for more information.

Benefits for Sites

A constant flow of leads from FOMAT Medical Research and valuable networking opportunities.
Appropriate compensation for each study enrolling.
The aid of trained and experienced research staff to help with all start up acticities (Regulatory/paperwork, contracts and budgets, conferences/Investigator meetings, monitor coordination, etc).
A network with other research sites in your community through FOMAT Medical Research partners.
Assistance from FOMAT Medical Research partnered sites through referrals for increased enrollment on hard to enroll studies.
Provided connections to local laboratories and customers who are already contracted for the development and results of clinical studies, with FOMAT Medical Research.
Training from dedicated FOMAT Medical Research staff.

Requirements for Sites

Have a designated space for FOMAT Medical Research coordinators for the development of clinical studies and a secure storage area for study information.
Provide the necessary resources for the study conduction.
Provide a price list for the basic services offered at your practice.
Allow access to a patient database for recruitment and reviewing purposes for study enrollment.
Local MOH Approval for Medical Research in your facilities. In applicable countries*
Work exclusively with FOMAT Medical Research as your only Site Management Organization (SMO).

Contact us for PIs