Stefanie Parker Email & Phone Number

Kansas City, Mo, Us

Palo Alto, Ca, Us

Seattle, Washington, Us

• Provide day-to-day coordination of clinical research studies including screening patients for protocol eligibility, ensuring informed consent has been properly obtained, enrolling subjects, collecting data, and communicating with clinic staff. • Provide technical direction to other in the department. Oversee the quality control aspects of the work performed.• Lead training, mentoring, workload planning, and assigning workflow to ensure requirements are met.

Seattle, Washington, Us

• Responsible for supporting the development of policies and procedures that detail roles and responsibilities of various institutions and programs including but not limited to (1) SCCA clinical operations staff, (2) SCCA staff from other departments who provide research related services to SCCA and affiliate institutions, and (3) Fred Hutchinson Cancer Research Center or University of Washington departments that collaborate on research.• Responsible for working with faculty and staff from UW/Fred Hutch Cancer Consortium disease site programs to operationalize and integrate clinical trials at both Network Affiliate and/or Community Sites. This work includes but is not limited to trial implementation, operational support, and study specific processes.

Seattle, Washington, Us

• Mentor other coordinators and serve as an education and training resource to others in the ongoing development of clinical research knowledge and experience.• Develop department and/or protocol standard operating procedures and tools.• Lead the startup of studies including things such as budget development, contracting, and protocol implantation.

• Oversee/manage in-house team of three coordinators.• Responsible for creating SOP’s and other site-specific documentation (i.e. guidelines, unaffiliated sites agreements, etc.).• Work closely with physicians, coordinators, research nurses, and intensive therapy unit nurses to ensure all study specific procedures are completed per protocol.• Provide support to research coordinators and act as back up for all 85+ federally funded oncology studies which included a verity of different diseases sites including but not limited to; gynecological, gastrointestinal, hematology, melanoma, breast, thoracic, genitourinary, neurology, head and neck, cancer care delivery, quality of life, etc

• Coordinate federally funded group oncology research studies which include but are not limited to NRG, SWOG, Alliance, and ECOG, while ensuring adherence with FDA code of federal regulations, Good Clinical Practice (GCP) and ICH guidelines.• Responsible for communicating changes in site/program management requirements to all PCRC NCORP component/subcomponent sites.• Monitor and maintain information from PCRC NCORP component/subcomponent sites regarding patient accrual information and study specific training completion.• Ensure that all new SWOG research staff for Swedish Cancer Institute and PCRC NCORP component/subcomponent sites have completed all required training and register them into the appropriate systems.

• Coordinate phase II-IV clinical trials for the following indications: Treatment Resistant Depression, Major Depressive Disorder, Binge Eating Disorder, and Attention Deficit Hyperactive Disorder, Post-Traumatic Peripheral Neuropathic Pain.• Initiation, operation, and completion of protocols in accordance with FDA code of federal regulations, Good Clinical Practice (GCP) and ICH guidelines.• Responsible for ensuring that subject charts are prepared for upcoming visits, as well as ensuring that enrollment logs, investigational product logs, and subject identification logs are all current and accurate.• Evaluate subject eligibility and obtaining informed consent. Responsible for conducting study visits, dispensing drug, and ensuring protocol compliance.

• Assist in coordinating phase II-IV clinical trials for the following indications: Major Depressive Disorder, Treatment Resistant Major Depressive Disorder, Sexual Dysfunction Disorder, Bipolar, Binge Eating Disorder, and Attention Deficit Hyperactive Disorder.• Assist in the initiation, operation, and completion of protocols in accordance with FDA code of federal regulations, Good Clinical Practice (GCP) and ICH guidelines.• Responsible for preparing subject charts for upcoming visits as well as updating enrollment logs, investigational product logs, and subject identification logs.

Abilene, Tx, Us

• Ensure all new pre-paid funeral and life insurance contracts were processed in a timely manner• Assist in requesting and following up on previous requested medical records• Handle weekly and monthly commission reports• Send out weekly and monthly checks and commission statements to agents and funeral homes

Mba-Healthcare Management, Health/Health Care Administration/Management

Bachelor'S Degree, Psychology