VIVIANA MORENO

• Enhanced clinic efficiency by streamlining appointment scheduling and follow-up processes.
• Collaborated with specialists for comprehensive patient care, resulting in improved health outcomes.
• Reduced hospital readmission rates by implementing effective preventive care measures and treatment plans.
• Conducted physical examinations and diagnostic tests to accurately diagnose patients'' medical conditions.
• Performed minor surgical procedures, ensuring optimal patient safety and comfort throughout the process.
• Educated patients on disease prevention and healthy lifestyle choices, contributing to overall community wellbeing.
• Maintained detailed and accurate electronic health records for efficient information retrieval and communication among healthcare providers.
• Developed treatment plans tailored to individual patients'' needs, considering their medical history, personal preferences, and financial constraints.
• Provided ongoing support to patients with chronic illnesses by monitoring their progress and adjusting treatment plans as necessary.
• Participated in continuing education programs to stay current on the latest advancements in medical knowledge and technology.
• Promoted a culture of patient-centered care within the practice, resulting in increased patient loyalty and referrals from satisfied clients.

• Enhanced clinic efficiency by streamlining appointment scheduling and follow-up processes.
• Improved patient satisfaction by providing thorough and compassionate care during consultations.
• Collaborated with specialists for comprehensive patient care, resulting in improved health outcomes.

Provide diagnoses and care for health issues rooted in the Endocrine System .

Schedule follow up for the next visit of patients .

Help with the disgnoses digestive disorders include liver diseases , ulcers , irritable bowel syndrome and cancer.

• Working knowledge of clinical trials, Federal, State, and local regulations, consent form and protocol development
• Knowledge of Good clinical practices (GCP), food and Drug Administration (FDA) Regulations, NIH guidelines, and HIPAA regulations
• Interact with principal and sub-investigators, research nurses and patients in the clinical setting
• Data collection and entry
• Interactions with the Clinical Trials sponsoring industry and other Cancer Research Organizations to address protocol compliance, subjects’ status and enrollment through on-site visits
• Knowledge Interpersonal Skills, Communication Skills, IRB, Accuracy, Compliance and Database
• Maintain current and accurate protocol documentation, update investigators and other team members of pertinent protocol changes
• Notifies direct supervisor about concerns regarding data quality and study conduct
• Independently works external study monitor and / or auditors
• Recruit and screen potential study participants and perform intake assessments for assigned trials
• Professional communications with sponsors and all the team
• Works closely with a regulatory Coordinator or directly with the institutional Review Boards (IRB) to submit adverse events, Serious Adverse Event, Protocol deviations and safety letters in accordance with local and federal guidelines
• In the collaboration with the Physician following changes about the conditions of the patient, adverse events, new concomitant medicine, new procedures

• Improved organizational efficiency by streamlining volunteer onboarding processes.
• Enhanced community engagement by organizing and leading outreach events.
• Mentored new volunteers, fostering a supportive and inclusive team environment.
• Coordinated volunteer training sessions to ensure consistent delivery of services across teams.

• Identified issues, analyzed information and provided solutions to problems.
• Developed and maintained courteous and effective working relationships.
• Paid attention to detail while completing assignments.