For Sponsors & CROs

 

Therapeutic Capabilities

The following are capability and feasibility areas. They are not a list of active trials.

  • Pulmonology
  • Obesity Medicine
  • Rheumatology
  • Sleep Disorder
  • Women’s Health
  • Family Medicine
  • Internal Medicine
  • Dermatology
  • Cardiology
  • Endocrinology
  • mRNA Studies
  • Otolaryngology (ENT)
  • Gastrointestinal System (GI)
  • Infectious Disease and Vaccines
  • Neurology
  • Immunology and Inflammation
  • Psychological Conditions (Mental Health)
  • Oncology
  • Nephrology
  • Psychiatry
  • Genitourinary System
  • Musculoskeletal System
  • MASLD/MASH
  • Men’s Health

Documented experience is listed separately, and includes asthma, COVID-19 vaccine, and lupus.

Facility and Equipment

  • Ambient centrifuge
  • Lab freezer, minus 20 degrees Celsius
  • Low-temperature freezer, minus 70 degrees Celsius
  • Health-o-Meter physician scale
  • Mortara electrocardiograph
  • Diagnostic set with otoscope and ophthalmoscope heads
  • Private exam rooms
  • On-site lab
  • Temperature-controlled investigational product storage with continuous monitoring
  • Refrigerated investigational product storage, 2 to 8 degrees Celsius
  • Alarm notification
  • Daily temperature logs
  • Locked pharmacy area with accountability logs
  • Backup generator

Site Capability in Detail

Staff Certification

Site staff are trained and certified for their clinical research roles, and the site maintains a dedicated quality control function.

IRB

The site is central IRB capable.

Data Systems

The site uses secure, HIPAA-compliant data systems for study records and participant information.

Equipment Calibration

Site equipment is maintained and calibrated for clinical research use.

IP Storage and Monitoring

Investigational product is stored in temperature-controlled storage with continuous monitoring, refrigerated storage at 2 to 8 degrees Celsius, alarm notification, and daily temperature logs. The pharmacy area is locked, with accountability logs.

Patient Population

The site serves a diverse Miami community, from the 4,500 plus database.

Recruitment Systems

Recruitment uses database outreach, physician referrals, and recruitment vendors.

Quality and Audits

The Quality Control Department supports accuracy, consistency, and compliance, and the site supports audits and monitoring visits.

Safety and Facilities

The site has private exam rooms, an on-site lab, a locked pharmacy area, and a backup generator.

Languages

Services are available in English and Spanish.

Recruitment

Recruitment is supported by database outreach, physician referrals, and recruitment vendors. The site database includes 4,500 plus HIPAA-compliant records, which supports identification of potential participants for feasibility review.

Steps for Sponsors and CROs

  1. Contact the site using the Sponsor/CRO Contact form on this page, or by phone or email.
  2. Share the protocol and study information for feasibility review, including the therapeutic area and population needed.
  3. Complete start-up, including central IRB review and contracting, with a 4 to 6 week start-up timeline.
  4. Begin enrollment and study conduct with the site investigators and coordinators, with quality control and monitoring support.
  5. Continue communication through study conduct, monitoring visits, and closeout.

Contact

14335 S.W. 120 ST, Suite 209, Miami, FL 33186. Phone: 305-705-7052. Fax: 305-705-7791. Email: roman@phoenixresearchcenter.com.

For general questions, the General Contact form on the home page is also available as an alternative. For sponsor and CRO inquiries, please use the Sponsor/CRO Contact form above.