Sandhya Pendyala Email & Phone Number

Ann Arbor, Michigan, United States

Department of Internal Medicine• Managed patient recruitment, informed consent, and enrollment for liver cancer trials, ensuring clear communication and ethical standards.• Collected and entered trial data accurately, maintaining patient information and results in liver cancer studies using EPIC.• Conducted EPIC reviews to identify eligible patients for liver cancer trials and track study-related data.• Assisted with collecting vital signs, imaging data, and blood samples, including biomarkers for liver cancer screening.• Handled all aspects of liver cancer trials, ensuring protocol adherence and regulatory compliance.• Preparation and submission of IRB applications and amendments to get approvals and maintain ethical compliance.• Supported participants by providing education, follow-up, and ongoing care throughout the study.• Coordinated multiple liver cancer trials at the same time, managing timelines, budgets, and resources effectively.

Dearborn, Michigan, United States

Department of Cardiology• Coordinated patient recruitment, informed consent, and enrollment, emphasizing clear communication and ethical considerations.• Collected, organized, and entered trial data accurately into databases, maintaining the integrity of patient information and trial results.• Worked closely with principal investigators, cardiologists, and healthcare teams to ensure smooth trial execution.• Performed in the collection of vital signs, EKG, and processing of blood.• Managed all aspects of clinical trials, from initiation to closeout, ensuring protocol adherence and regulatory compliance• Ensured all study-related activities complied with institutional review boards (IRBs), Good Clinical Practice (GCP), and FDA regulations.• Provided patient-centered care through support, education, and follow-up for participants throughout their involvement in the study.• Successfully coordinated multiple cardiology studies simultaneously, managing timelines, budgets, and resources efficiently.• Conducted internal audits and monitored studies to ensure data quality and adherence to study protocols.

Fairborn, Ohio, United States

Department of Dermatology • Actively participates in the informed consent process of study subjects, ensuring comprehension, voluntariness, and ethical conduct throughout.• Committed to supporting the safety of clinical research patients and participants, promptly reporting adverse events and ensuring swift and appropriate responses.• Proficient in preparing and maintaining comprehensive clinical trial source documents, fostering accuracy and integrity throughout the research process.• Scheduling and monitoring site visits, ensuring all documentation and procedures comply with regulatory requirements and study protocols.• Protects patient confidentiality and safeguards operations by managing sensitive information, fostering trust and compliance with privacy regulations.

Ohio, United States

Fairborn, Ohio, United States

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Andhra Pradesh, India

Master'S, Pharmacology And Toxicology-Clinical Trials Coordination, A

Pharmaceutical Sciences, A