For Sponsors

STAAMP Research

STAAMP Research has the capability to conduct clinical trials in a multitude of therapeutic areas, and design types. We work with major pharmaceutical and device sponsors, CROs, as well as smaller biotech and start-up companies to successfully and safely advance their research & development projects. STAAMP Research provides exceptional value to sponsors with rapid start-up capabilities, successful recruitment strategies, an experienced clinical research team, rapid data entry and dedicated quality control.

If you would like to partner with us, please reach email raul@staampresearch.com

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Collaborative Research Network + Partners

At STAAMP Research, our effort to create awareness within the industry and community has allowed us to meet/partner with outside research organizations with extensive research knowledge and expertise. Throughout this process, STAAMP Research has played an integral role in several aspects of research trial conduct with various industry leading organizations.

Therapeutic Expertise

Allergy & Immunology
Pediatrics
Pulmonology
Vaccines
Long Term Interventional & Observational

Family Medicine
Diabetes & Endocrinology
Cardiology
Gastroenterology
Women’s Health

Pain Management
Neurology
Psychiatry
Late Phase
Early Phase

Our Facility

Site Capabilities
Ability to scale based off individual protocol need	ACLS trained staff	Bilingual staff (English and Spanish)	-80º/-20ºC Freezers
Expedited startup, contract and budget, and enrollment capabilities	Multiple locations with unique patient populations	Lab Technicians	Refrigerators
Partnerships with various specialty physicians and medical imaging centers	Located in and within close distance of major hospitals	Proprietary SOPs, processes and procedures	Continuous temperature monitoring devices
CLIA certified laboratory	Crash Carts	Quality Control Systems	Ambient/refrigerated centrifuges
Highly educated/experienced and trained staff	Access to multiple EMR and research databases	Quality Assurance Systems/CAPA	Limited access, temperature-controlled, document and drug storage
GCP certified/IATA certified	Clinical research coordinating staff consisting of international medical graduates	Fully calibrated equipment and certificates	DEA drug compliance

Site Capabilities:

Ability to scale based off individual protocol need
Expedited startup, contract and budget, and enrollment capabilities
Partnerships with various specialty physicians and medical imaging centers
CLIA certified laboratory
Highly educated/experienced and trained staff
GCP certified/IATA certified
ACLS trained staff
Multiple locations with unique patient populations

More Capabilities
- Located in and within close distance of major hospitals
- Crash Carts
- Access to multiple EMR and research databases
- Clinical research coordinating staff consisting of international medical graduates
- Bilingual staff (English and Spanish)
- Lab Technicians
- Proprietary SOPs, processes and procedures
- Quality Control Systems
- Quality Assurance Systems/CAPA
- Fully calibrated equipment and certificates
- -80º/-20ºC Freezers
- Refrigerators
- Continuous temperature monitoring devices
- Ambient/refrigerated centrifuges
- Limited access, temperature-controlled, document and drug storage
- DEA drug compliance

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Our Process

Our unique methods and processes here at STAAMP Research have allowed us to efficiently conduct numerous studies throughout the years. Our recruitment process sets us apart from other standalone clinical research sites as we have the patient volume to fill even the most complex protocols.

The patients that participate in our trials are seen by a Clinical Research Coordinator and Investigator at every visit. This ensures that their needs are being met at all stages of the trial process, but most importantly, to ensure the safety of the patient. Every member or our clinic staff has an established rapport with the patients we see here which creates a very trustworthy environment and allows for an effortless transition into a discussion about clinical trials if the physician feels there’s a benefit to the patient.

The relationship that we’ve established with our patients has allowed us to retain a high percentage of study participants in long- and short-term trials. Our staff prioritizes retention by frequently contacting subjects throughout the study process and engaging them at every clinic visit. Education is also a priority as it keeps patients engaged and aware of the process. It is our goal to provide quality care to our patients and having these processes set at every stage allows us to focus and enhance the patient experience.

Patient Recruitment

STAAMP Research is able to identify potentially qualified participants by utilizing our Electronic Medical Records system and robust research specific database within the site Clinical Trial Management System. Criterion matching reports are utilized to locate potential subjects meeting specific inclusion/exclusion criteria and multiple contact methods such as phone, email and TEXT are utilized to notify potential candidates of study opportunities. These combined databases and processes allow STAAMP Research to consistently exceed enrollment targets.