Utilizing my extensive Healthcare and Clinical Research career, non-profit involvement over the past decades, side hustle jobs and life experience along with my "official" education to consult, coach, mentor and advise clients in the pursuit of their passions and calling.

Clinical and Translational Science Institute

Clinical and Translational Sciences Institute

Clinical Research Consultant focusing on improving clinical research, patient access to healthcare information, and promotion of community events to celebrate cancer survivorship.Services provided:* Clinical research monitoring and protocol management within an interactive team environment.* Clinical protocol development and integration consultations, focusing on protocol development to minimize projected and current data/safety risks, optimize data collected, and ensure all goals are collaboratively achieved. * Objective assessment of compliance risks: protocol, site, & patient.* Analysis of potential risks with timelines and timelines related to planned and required data analysis and reporting.* Quality assurance auditing, on-site FDA, ICH-GCP compliance reviews* Healthcare Informatics & EDC system review and testing* Perform public educational seminars on health promotion and maintenance

Clinical Project Manager of "Expanded"​ Phase I Oncology Clinical Trial, and several other Phase I/II clinical trials in closeout stages. Clinical Project Manager functions performed beyond the "basic" expectations:*Accessed client specific financial software of expenditures*Accessed client specific version of well-known EDC program to perform overall review*Performed CRA, CTM, and PM roles concurrently. *Facilitated meetings within team and client as required within an active, traveling team (fluctuating schedule) as required.

Senior Clinical Trial Manager of Phase I/II Oncology Clinical Trials for Solid Tumors and Hematological Malignancies from active enrollment, expansion, through successful on-time study closure.Resource and Certified Trainer for outside vendor EDC reporting systemDirect Involvement of assigned Phase I Solid Tumor/Hematological Malignancy and/or Solid Tumor Trials to ensure successful deliverables on or before expected timelines.Achieved preferred provider status with client within 5 months of study assignmentActively worked with team members to manage complex Phase I/II Hematology/Oncology trials with optimal data driven timeline results including database locks.Performed EDC data reviews to ensure logical data, within client driven timelines. Client resource to review protocol amendment changes based on my extensive Oncology/Clinical Trial Research experience, which includes direct Oncology patient care experience (as referred to below).Mentored other CTMs and other team members.

In this position, my role was to manage Phase I/II Hematological Malignancy/Solid Tumor Clinical Trials.As CTM, my responsibilities included * Manage all clinical aspects related to my assigned projects and report appropriately to upper management, the client, and my team. ^ Monitor Clinical Trial Operations budget* Perform site visits for training, assessment, and site support as necessary. * Cross functional departmental communication on a continual basis to ensure a high quality result was provided.* Effectively learned acquired company's systems and assisted with the integration of employee transition to Novella CTMS and related systems.

Project Manager for Phase I/III Hematological Malignancy and Solid Tumor Oncology Clinical Trials from study start-up through study closure and Phase III Metastatic Breast Cancer Clinical Trial during active enrollment, expansion to study closure.

Responsible for management Oncology Phase I/III Solid tumor protocols. * Coordination and management of the Clinical Research Team in conjunction with the contracted functional groups.* Directed technical and operational aspects of the project to ensure compliance with company policies and procedures* Ensured project specific and therapeutic training to clinical project teams conducted initially with project team members and ongoing as required/necessary* Managed the contractual budget, actual costs, including personnel hours and project needs to determine the most cost effective and efficient means to ensure that all project deliverables met the client’s needs and adhered to the contract. When needed, a change in contractual scope was initiated and followed through until completion.* Participated in project team and executive review meetings to communicate progress of studies, quality issues, budgetary issues, and operational concern* Provided regular updates to clients of study status and per the company management reporting system.* Ensured projects complied with ICH, GCP, FDA CFR, and company policies.* Responsible for orchestrating internal and external project team meetings across internal and external clients and vendors. .

Lead Clinical Research Associate of Phase III Oncology,Multi-center Metastatic Breast Cancer Clinical Trial.

Lead Clinical Research Associate on Oncology Phase I/II Acute Myelogenous Leukemia and Phase III Metastatic Breast Cancer Clinical Trials.

• Contracted as Clinical Research Associate for the National Gaucher Registry, National Fabry Registry, and Arizona Gaucher Support Network. Developed Informed Consent for patients participating in Phase IV Clinical trials. • Nurse Lecturer for Omni Network. Patient education seminars on better bone health for patients with Multiple Myeloma, Breast Cancer, and Prostate Cancer. • Nurse Lecturer for Aventis Pharmaceuticals. Nurse education seminars on taxanes.

Clinical Research Manager of Public Health Research Unit focused on Smoking Cessation Clinical Trials.

Performed all clinical data monitoring, cleaning, and query resolution for company's Phase I-II Auto Immune Phase I-II Clinical Trials.

Research Nurse for Phase I-III Solid Tumor and Hematological Malignancy Clinical Trials. * Assessed patients for eligibility, ensured Informed Consent, performed direct patient care assessments, administered Investigational treatments, scheduled all protocol and standard of care required procedures, exams, and nursing visits, performed pharmacokinetic specimen draws, processing, storage, and shipment to appropriate facility. Provided resource support to physicians and patients regarding CAMS.

Lead Nurse at satellite out-patient Oncology-Hematology Clinic•Facilitated transition of clinic from private practice to US Oncology satellite office. •Mixed and administered chemotherapy, biologics, enzyme replacement, and other supportive care therapy to patients.•Responsible for ICD-9 coding of all clinical procedures performed •Managed clinical supply inventory including ordering pharmaceutical supplies for clinic, including chemotherapy, biologics, supportive medications, administration supplies, and physician clinic supplies.•Provided patient healthcare educational sessions for Oncology, Hematological Malignancies, Gaucher Disease, Supportive therapies, symptom management, and Better Bone Health care for patients and supportive caregivers.