Suburban Research Associates
Suburban Research Associates (SRA) is a leading site for psychiatric and medical research, conducting over 250 clinical trials since 1999. Their mission is to advance medical science by providing innovative research opportunities while ensuring participant safety and well-being. They collaborate with healthcare providers, sponsors, and community organizations to facilitate cutting-edge treatments, support community health initiatives, and contribute to scientific progress. They offer a range of studies in psychiatry, neurology, and other medical fields, with a focus on improving health outcomes and developing new therapies.
Industries
Nr. of Employees
small (1-50)
Suburban Research Associates
Media, Pennsylvania, United States, North America
Services
On-site conduct of investigator-led and sponsor-sponsored clinical trials across psychiatric, neurology, metabolic and vaccine indications, including participant assessments, protocol execution, safety monitoring and sponsor reporting.
Recruitment campaigns, online interest/registration forms, pre-screening and eligibility assessment to build study-specific cohorts and manage waitlists.
Operational support for participants including HIPAA-compliant transportation coordination, 24/7 access to psychiatric providers and structured aftercare including limited-duration medication management.
Partnerships with local advocacy groups and community organizations to support outreach, caregiver events and condition-specific education to enhance recruitment and participant support.
Operational processes to conduct IRB-reviewed studies, maintain ethical oversight and protect participant confidentiality consistent with regulatory expectations.
On-site conduct of investigator-led and sponsor-sponsored clinical trials across psychiatric, neurology, metabolic and vaccine indications, including participant assessments, protocol execution, safety monitoring and sponsor reporting.
Recruitment campaigns, online interest/registration forms, pre-screening and eligibility assessment to build study-specific cohorts and manage waitlists.
Operational support for participants including HIPAA-compliant transportation coordination, 24/7 access to psychiatric providers and structured aftercare including limited-duration medication management.
Partnerships with local advocacy groups and community organizations to support outreach, caregiver events and condition-specific education to enhance recruitment and participant support.
Operational processes to conduct IRB-reviewed studies, maintain ethical oversight and protect participant confidentiality consistent with regulatory expectations.
Expertise Areas
- Clinical trial management
- Psychiatric clinical research
- Neurology clinical research
- Pediatric and rare disease trials
Key Technologies
- Online enrollment and interest-list forms
- HIPAA-compliant third-party transportation coordination
- IRB-reviewed protocol-driven trial conduct
- SMS/phone-based scheduling and ride notifications
News & Updates
An article discussing the complexities of Alzheimer’s disease and its impact beyond memory loss.
An article explaining the classification of traumatic events as PTSD.
An article providing information about Type 1 Diabetes.
An article explaining the process, safety, and importance of clinical trials.
Information about the criteria used to determine eligibility for research studies.
An article discussing the complexities of Alzheimer’s disease and its impact beyond memory loss.
An article explaining the classification of traumatic events as PTSD.
An article providing information about Type 1 Diabetes.
An article explaining the process, safety, and importance of clinical trials.
Information about the criteria used to determine eligibility for research studies.