Marisha W. Email & Phone Number

Yukon, OK, US

• Manage 15+ members of clinical staff involved in clinical research operations.
• Act as liaison between clinical infusion team and research team for both early and late phase clinical trials.
• Devise, evaluate, implement, and streamline protocols and standards of infusion clinic; directs the planning, implementation and evaluation of patient care programs for the patient populations served in the Infusion.
• Prepare and administer revenue and operating budgets, personnel management, program development and quality assurance.
• Assures delivery of quality patient and family care and to promote education and research.
• Maintains strong relationships with the all areas and clinicians to achieve the programmatic goals for the Research Infusion Center, the department of nursing and the organization.

• Responsible for the coordination of direct patient care, including treatment administration, patient/family education, and adverse event assessment in accordance with clinical study protocols.
• Provided leadership through activities such as preceptor role, informal and formal leadership roles, and quality improvement efforts.
• Delegated patient care according to skill level, experience, patient acuity, fiscal accountability and availability of resources.

• Administered chemotherapy, biologic agents, & additional drugs.
• Managed oncology patients on early phase clinical trials at the Stephenson Cancer Center.
• Collaborated with data and research team, provide query resolution, attend PSV/SIV meetings,and communicated with sponsors regarding treatment related issues.
• Facilitate dose modification by assessing patient, assessing labs, consulting protocol ortreatment plan, calculating dose, and consulting physician regarding dosage modifications, problems and symptom management.

• Participated in recruitment and selection of study participants by interviewing and documenting medical history to determine compliance with eligibility requirements.
• Ensure assigned studies were conducted in accordance with the Food and Drug Administration (FDA), Office for Human Research Protections (OHRP), and Good Clinical Practice (GCP) guidelines.
• Interfaced with research participants to support efforts to determine eligibility and consenting of study participants according to protocol.
• Communicated and collaborated specific study requirements to the research team, including internal and external parties, sponsor, monitors, PI, and study participants.
• Maintained compliance with research protocols, by providing ongoing quality control audits, including maintaining ongoing investigational drug accountability.
• Participated with the PI and study team to identify and prioritize the development of systems and infrastructure to maintain research quality and compliance.

Master Of Nursing, Clinical Nurse Specialist

Bsn, Registered Nursing/Registered Nurse

Activities and Societies: Sigma Theta Tau, Alpha Chi Honor Society