Ramona Rosario
Frederick,MD
Summary
Equipped with strong problem-solving abilities, willingness to learn, and excellent communication skills. Poised to contribute to team success and achieve positive results. Ready to tackle new challenges and advance organizational objectives with dedication and enthusiasm.
Overview
37
37
years of professional experience
Work History
Diagnostic Medical Sonographer
Chesapeake Urology
12.2001 - Current
- Assisted in training new sonographers, sharing expertise in imaging techniques and best practices for patient care.
- Reviewed physicians' orders to determine medical imaging needs and operated radiologic equipment to capture, develop, and produce diagnostic images.
- Educated patients on procedure details, provided instructions, and answered questions to minimize anxiety and improve cooperation.
- Optimized image quality through meticulous attention to detail and appropriate selection of transducers, settings, and display parameters.
- Collaborated with radiologists to provide accurate and timely diagnostic information for various medical conditions.
- Promoted patient safety by adhering to infection control protocols and proper equipment usage guidelines.
- Provided exceptional patient care by adapting examination techniques to accommodate patients with special needs or unique circumstances.
- Enhanced patient comfort by ensuring a thorough explanation of sonographic procedures before beginning examinations.
- Fostered a positive work environment through open communication, teamwork, and a commitment to continuous improvement within the diagnostic medical sonography profession.
- Reduced patient anxiety by establishing rapport with patients and addressing any concerns prior to starting an examination procedure.
- Monitored and managed inventory and supply levels of sterile and non-sterile items, contrast materials, catheters, films, and chemicals.
- Improved diagnostic accuracy by maintaining up-to-date knowledge on innovative ultrasound techniques and technologies.
- Participated in quality improvement initiatives aimed at enhancing the overall performance of the sonography department within the healthcare facility.
- Maintained equipment functionality by conducting routine inspections, troubleshooting issues, and coordinating repairs when necessary.
- Advocated for patient safety by strictly adhering to hygiene and disinfection protocols for sonography equipment.
- Ensured maintenance of sonography equipment, leading to consistent image quality and reduced downtime.
- Customized sonographic examination techniques according to patient needs, enhancing comfort and cooperation.
- Streamlined sonographic procedures, optimizing workflow and increasing number of daily patient examinations without compromising quality.
- Facilitated compassionate environment, addressing patient queries and concerns with empathy and professionalism.
- Contributed to significant decrease in diagnostic errors by implementing double-check system for sonographic images.
- Enhanced patient comfort and cooperation during sonographic procedures by providing clear explanations and gentle guidance.
- Trained new sonographers in best practices, enhancing team proficiency and patient care standards.
- Maintained up-to-date knowledge of sonographic technology and techniques, ensuring delivery of high-quality diagnostic services.
- Collaborated with healthcare teams to develop patient care plans, improving outcomes with timely sonographic findings.
- Led quality assurance efforts for sonographic services, ensuring adherence to industry standards and regulations.
- Enhanced patient satisfaction, attentively addressing concerns and providing reassurance throughout sonographic process.
- Supported radiologists in diagnosing and treating diseases, preparing detailed sonographic reports for review.
- Played key role in early detection of critical conditions through meticulous sonographic examinations.
- Upheld legal standards, HIPAA requirements and facility guidelines by obtaining written consent and securing patient information.
- Submitted written reports, verbal summaries, photographs and recordings to physicians to support accurate medical decision making.
Clinical Research Coordinator
Urological Consultants
12.2000 - 12.2009
- Followed clinical research protocols and conducted study visits in compliance with ICH/GCP and FDA regulations.
- Screened patient records, databases, and physician referrals to identify prospective candidates for research studies.
- Gathered, processed, and shipped lab specimens.
- Enhanced patient safety by meticulously monitoring and documenting adverse events during clinical trials.
- Followed informed consent processes and maintained records.
- Collaborated with clinical staff and other healthcare professionals to support clinical trial data accuracy.
- Coordinated and monitored clinical trial activities to support timely and accurate completion of studies.
- Worked with principal investigator and sponsors to facilitate daily trial activities and comply with research protocols.
- Facilitated clear communication between principal investigators, sponsors, and study participants for seamless trial execution.
- Assessed patients'' eligibility criteria following strict adherence to inclusion/exclusion guidelines.
- Trained new team members on essential clinical research protocols and procedures, promoting a culture of continuous learning.
- Maintained compliance with protocols covering patient care and clinical trial operations.
- Managed patient recruitment, informed consent process and data entry to support trial objectives.
- Increased participant retention rates through proactive follow-up efforts and regular engagement activities.
- Developed and maintained accurate and up-to-date case report forms and source documents.
- Prepared and maintained regulatory documents for clinical trial submissions.
- Oversaw the management of investigational product supplies, ensuring appropriate storage conditions were maintained at all times for optimal efficacy during trials.
- Collected data and followed research protocols, operations manuals, and case report form requirements.
- Reduced data entry errors by implementing stringent quality control measures throughout the study lifecycle.
- Developed strong relationships with trial sponsors, ensuring ongoing collaboration and future project opportunities.
- Maintained accurate and up-to-date case report forms and source documents for traceability.
- Monitored patient safety throughout clinical trials and reported any adverse events.
- Participated in initiation visits and investigator meetings, implementing trials following study timelines and budgets.
- Assisted in drafting comprehensive research reports summarizing findings, conclusions, and recommendations for further action.
- Contributed to the successful completion of clinical trials by proactively resolving issues, mitigating risks, and meeting deadlines in a fast-paced environment.
- Prepared detailed informed consent documents to clearly communicate risks, benefits, expectations, rights and responsibilities related to participation in clinical trials.
- Maintained compliance with regulatory guidelines through rigorous documentation and protocol adherence.
- Directed site initiation visits, establishing key partnerships with local healthcare providers to facilitate successful trial implementation.
- Implemented electronic data capture system, significantly reducing paper use and increasing data retrieval efficiency.
- Improved trial visibility and public interest through effective community outreach and education initiatives.
- Conducted comprehensive reviews of clinical trial protocols to identify and rectify potential issues before study initiation.
- Streamlined patient visit schedules, reducing wait times and increasing patient satisfaction.
- Collaborated with biostatisticians to analyze trial data, contributing to meaningful study findings.
- Facilitated successful trial completion by closely monitoring study timelines and milestones, ensuring on-time delivery of results.
- Streamlined process for serious adverse event reporting, enhancing safety monitoring efforts.
Foreign Medical Doctor
Dr Lawrence Roach , PA
12.1987 - 12.1998
- Diagnosed and treated patients suffering from chronic conditions.
- Established strong relationships with patients and their families, fostering trust and commitment to the healthcare plan.
- Educated patients and families on benefits of healthy diet and adequate exercise.
- Collaborated with multidisciplinary teams to develop comprehensive care plans for complex patients.
- Reviewed patient allergies, problems, medications, and immunization statuses.
- Conducted thorough physical examinations and diagnostic tests, leading to accurate diagnoses and timely medical interventions.
- Participated in continuing education opportunities keeping up-to-date with advancements within respective fields remaining competitive amongst peers.
- Enhanced clinic efficiency by streamlining patient flow and optimizing appointment scheduling.
- Improved patient satisfaction by providing empathetic care and clear communication of treatment plans.
Education
M.D. - General Medicine
Nordestana University
Dominican Republic02.1978
Skills
Diagnostic imaging
- Certified in CPR/AED
- Patient care
- Teamwork and collaboration
- Problem-solving
- Time management
- Attention to detail
- Multitasking Abilities
- Reliability
- Excellent communication
- Organizational skills
- Adaptability and flexibility
- Medical terminology
- Professionalism
- Continuous improvement
Fluent in Spanish
I'm able to translate, write reports and correspond with Spanish speaking patients.
My bilingual skills allow me to speak, listen, and write in any medical setting.
Languages
Spanish
Native or Bilingual
Timeline
Diagnostic Medical Sonographer
Chesapeake Urology
12.2001 - Current
Clinical Research Coordinator
Urological Consultants
12.2000 - 12.2009
Foreign Medical Doctor
Dr Lawrence Roach , PA
12.1987 - 12.1998
M.D. - General Medicine
Nordestana University
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