Experience

CITY OF PASADENA PUBLIC HEALTH DEPARTMENT

• United States
• Hospitals and Health Care
• 1 - 100 Employee

• Registered Nurse

  • Oct 2020 - Present

  Working with the contact tracing team and the school team Working with the contact tracing team and the school team



Mulay Educational and Clinical Consulting Associates

• Consultant

  • Sep 2000 - Present

  Nationally and internationally recognized nursing thought leader in clinical research and novel therapeutics. Consultant and speaker on various types of solid tumor cancers as well as clinical trials design and management. Nationally and internationally recognized nursing thought leader in clinical research and novel therapeutics. Consultant and speaker on various types of solid tumor cancers as well as clinical trials design and management.


Eli Lilly and Company
• United States
• Pharmaceutical Manufacturing
• 700 & Above Employee
• Senior Clinical Research Scientist

  • Sep 2011 - Oct 2013


Premiere Oncology

• Medical Practices
• 1 - 100 Employee

• Director, Clinical Research Unit

  • Jul 2004 - Aug 2011

  •Serve as sub-investigator on all Phase I and II Clinical Trials •Collaborate with physician investigators on identification of research subjects and appropriate study placement •Manage a research team of NPs, RNs, Clinical Research Associates (data managers) and Research Assistants in the conduct of all studies oResponsible for the assignment of studies to staff based on skill levels and workload oProvide ongoing surveillance of each study to assure compliance with… Show more •Serve as sub-investigator on all Phase I and II Clinical Trials •Collaborate with physician investigators on identification of research subjects and appropriate study placement •Manage a research team of NPs, RNs, Clinical Research Associates (data managers) and Research Assistants in the conduct of all studies oResponsible for the assignment of studies to staff based on skill levels and workload oProvide ongoing surveillance of each study to assure compliance with protocol oConduct biweekly meetings with each staff member to assure open communication and assure consistent staff growth and development •Develop policies, procedures and forms oProvide ongoing assessment of the processes to assure compliance with FDA and GCP guidelines oDesign and create study specific source documents •Interact with sponsors including analysis of study procedures for clinical implementation prior to study initiation and as an ongoing process •Responsibility for preparation for all audits •Responsibility for all training and education of research team oDeveloped and maintain a policy and procedures manual for research activities oDesign and deliver power point presentations on a variety of topics to research and clinical staff •Provide direct care of research subjects including study-specific procedures such as physical examinations, punch biopsies oProvide clinical expertise to research department oIn-depth knowledge of the disease process and treatment modalities for all solid tumor cancers oUnique understanding of gastrointestinal stromal tumor, thyroid cancer, adenoid cystic carcinoma and a variety of other rare cancers Show less •Serve as sub-investigator on all Phase I and II Clinical Trials •Collaborate with physician investigators on identification of research subjects and appropriate study placement •Manage a research team of NPs, RNs, Clinical Research Associates (data managers) and Research Assistants in the conduct of all studies oResponsible for the assignment of studies to staff based on skill levels and workload oProvide ongoing surveillance of each study to assure compliance with… Show more •Serve as sub-investigator on all Phase I and II Clinical Trials •Collaborate with physician investigators on identification of research subjects and appropriate study placement •Manage a research team of NPs, RNs, Clinical Research Associates (data managers) and Research Assistants in the conduct of all studies oResponsible for the assignment of studies to staff based on skill levels and workload oProvide ongoing surveillance of each study to assure compliance with protocol oConduct biweekly meetings with each staff member to assure open communication and assure consistent staff growth and development •Develop policies, procedures and forms oProvide ongoing assessment of the processes to assure compliance with FDA and GCP guidelines oDesign and create study specific source documents •Interact with sponsors including analysis of study procedures for clinical implementation prior to study initiation and as an ongoing process •Responsibility for preparation for all audits •Responsibility for all training and education of research team oDeveloped and maintain a policy and procedures manual for research activities oDesign and deliver power point presentations on a variety of topics to research and clinical staff •Provide direct care of research subjects including study-specific procedures such as physical examinations, punch biopsies oProvide clinical expertise to research department oIn-depth knowledge of the disease process and treatment modalities for all solid tumor cancers oUnique understanding of gastrointestinal stromal tumor, thyroid cancer, adenoid cystic carcinoma and a variety of other rare cancers Show less


Cancer Institue Medical Group (The Angeles Clinic)
• Director, Clinical Research Unit

  • Sep 2002 - Jul 2004


UCLA

• United States
• Higher Education
• 700 & Above Employee

• Director, Novel Therapeutics Program

  • Aug 1996 - Sep 2002

  •Developed a comprehensive phase I research program including hiring and training RNs and Clinical Research Associates (data managers) •Authored a comprehensive orientation manual •Interacted with sponsors on the conduct of clinical trials and data collections •Responsible for preparation for all audits including three FDA audits •Developed a comprehensive phase I research program including hiring and training RNs and Clinical Research Associates (data managers) •Authored a comprehensive orientation manual •Interacted with sponsors on the conduct of clinical trials and data collections •Responsible for preparation for all audits including three FDA audits