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Southeastern Health Management

Respiratory Therapist (CRT / RRT) &ndash; Home Health Sehma (South Eastern Health Management Associates) Coverage Area: Broward County &amp; Miami-Dade County, FL Position Summary Sehma (South Eastern Health Management Associates) is seeking a licensed Respiratory Therapist (CRT or RRT) to provide respiratory care services in the home setting throughout Broward County and Miami-Dade County. We are willing to train motivated new graduates or therapists without home health experience. This role is responsible for respiratory equipment delivery, setup, patient education, clinical assessment, and documentation in a field-based environment. Compensation Starting Rate: $35 &ndash; $37 per hour (No experience required &ndash; training provided) Competitive compensation based on experience Full-time benefits package available Primary Responsibilities Deliver and set up respiratory equipment including: Oxygen concentrators Portable oxygen systems CPAP/BiPAP devices Nebulizers Ventilators Perform respiratory assessments in the home setting Educate patients and caregivers on proper equipment use, cleaning, and safety Monitor patient compliance and therapy effectiveness Communicate patient status updates to physicians and care teams Complete accurate documentation in EHR/EMR systems Ensure compliance with Medicare, Medicaid, and regulatory standards Travel throughout Miami-Dade and Broward Counties Participate in on-call rotation as needed Required Qualifications Active Florida CRT or RRT License Current BLS Certification Valid Florida Driver&rsquo;s License with reliable transportation Strong communication and documentation skills Ability to work independently in a field-based role Preferred Qualifications Home Health or Durable Medical Equipment (DME) experience Knowledge of oxygen therapy and PAP devices Familiarity with Medicare guidelines Bilingual (English/Spanish or Creole) strongly preferred due to South Florida patient population Core Competencies Patient-centered care Clinical assessment and critical thinking Accountability and professionalism Time management and self-motivation Regulatory compliance awareness Benefits (Full-Time Team Members) Medical, Dental, Vision Insurance 401(k) with employer contribution Paid Time Off and Company Holidays Employer-paid life insurance Comprehensive paid training program Career growth opportunities Work Location Field-based role covering: Miami Hialeah Kendall Homestead Fort Lauderdale Miramar Pembroke Pines Hollywood Plantation Surrounding Broward &amp; Miami-Dade communities

Respiratory Technician - Ambulatory

Position Title Oncology Clinical Research Coordinator (CRC) Position Type Full-Time Reports To Research Director / Principal Investigator Position Summary Total Health and Research Center (THRC) is seeking an experienced Oncology Clinical Research Coordinator (CRC) to support Phase IIV clinical trials in oncology and other therapeutic areas. The Oncology CRC will be responsible for the day-to-day coordination of clinical trials, ensuring protocol compliance, patient safety, regulatory adherence, and high-quality data collection. Key Responsibilities Study Coordination - Coordinate all aspects of clinical trials from site initiation through study close-out - Conduct protocol review and feasibility assessments - Prepare site for site qualification visits, site initiation visits, and monitoring visits - Ensure compliance with FDA, ICH-GCP, sponsor protocols, and IRB requirements Patient Recruitment and Screening - Identify and recruit eligible patients through EMR and physician referrals - Screen potential participants according to protocol inclusion/exclusion criteria - Schedule and coordinate screening procedures, labs, imaging, and biopsies - Conduct or assist with informed consent process Participant Management - Coordinate all study visits and treatment cycles - Track protocol visit schedules and treatment windows - Monitor participants for adverse events and safety signals - Ensure accurate concomitant medication tracking Oncology Treatment Coordination - Coordinate with infusion staff for investigational drug administration - Verify dose calculations and treatment schedules - Coordinate safety labs and pre-treatment requirements Data Management - Enter study data into EDC systems - Maintain source documentation and regulatory binders - Resolve data queries from sponsors and CROs Regulatory Compliance - Maintain regulatory documents including IRB submissions and protocol amendments - Ensure adherence to Good Clinical Practice (GCP) guidelines Monitoring and Audits - Prepare for monitoring visits, sponsor audits, and FDA inspections - Address monitoring findings and implement corrective actions Required Qualifications Education Bachelors degree in Nursing, Life Sciences, Health Sciences, Clinical Research, or related field. Experience Minimum 23 years experience coordinating oncology clinical trials. Experience with oncology protocols, infusion studies, RECIST imaging, and serious adverse event reporting preferred. Certifications (Preferred) - ACRP Certified Clinical Research Coordinator (CCRC) - SOCRA CCRP Certification - GCP Certification - Human Subjects Protection Training (CITI) Required Skills - Strong understanding of oncology clinical trial operations - Knowledge of ICH-GCP and FDA regulations - Experience with EDC systems - Strong organizational and time-management skills - Excellent patient communication skills

Oncology Clinical Research Coordinator (NOT REMOTE)

Join Southeastern Health Management and explore 2   exciting career opportunities. They're hiring for various roles with options for remote or on-site work. Apply today and become part of their innovative team.

Southeastern Health Management

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Respiratory Technician - Ambulatory

Oncology Clinical Research Coordinator (NOT REMOTE)