Sai Krishna Swayampu

• As a product operations specialist, I streamline and refine the patient-centered business in healthcare by transforming healthcare supply chains.
• Assisted in developing training materials for users of new products.
• providing data standardization and cleansing services for information sourced from IDN, MMIS, or ERP computer systems utilized in medical facilities.
• Reviewed, evaluated, classified, and conducted follow-up activities on all product complaints related to the nomenclature,identity, quality, reliability, safety, and effectiveness of medical devices and pharmaceutical drugs.
• Validating and enriching information from reputable sources such as Manufacturers, Access GUDID, US FDA, and various government registrations and suppliers' websites
• Identified and addressed risks, making necessary adjustments to the project plan.
• Conducted quality checks on work and ensured adherence to quality standards.
• Spearheaded the planning and development of project ideas, including defining project goals, scope, and deliverables, as well as creating project plans

• Spearheaded the management of clinical research projects across phases I-IV,
ensuring strict compliance with ICH-GCP guidelines.
• Managed and coordinated clinical research projects, ensuring adherence to
protocols, timelines, and regulatory guidelines.

• Conducted extensive research on pharmaceutical industry, including product terminology, drug nomenclature, and regulatory websites

• Demonstrated proficiency in utilizing various product databases such as Apollo Oracle interfaces, Cardinal Health, Owens and Minor, Medline, Pubmed, etc.

• Executed a comprehensive review and analysis of scientific and published documents to provide valuable support to the healthcare industry.
• Transformed raw clinical data into descriptive data structures for in-depth
analysis across diverse therapeutic areas.
• Utilized electronic data capture (EDC) systems for data entry, query
management, and database lock activities.
• Maintained compliance with applicable regulations, guidelines, and industry
best practices related to clinical research and data management.
• Contributed to process improvement initiatives to enhance data management
efficiencies and overall study quality.

• Created detailed reports on inventory levels and usage trends.
• Monitored storage areas for safety hazards and took corrective action when necessary.
• Supported purchasing activities by researching new vendors, negotiating contracts, and monitoring supplier performance.
• Analyzed supply chain operations to identify opportunities for improvement.
• Coordinated and facilitated the delivery of high-quality patient care, ensuring a seamless and positive healthcare experience.
• Acted as a liaison between patients, healthcare providers, and support staff,
  effectively communicating and addressing patient needs and concerns.
• Assisted patients in navigating the healthcare system, providing guidance on
  insurance coverage, referrals, and accessing appropriate healthcare resources.