Julia Brandt Email & Phone Number

Position supports the Healthcare Service division in the provision of clinical and technical writing to meet contract compliance and TRICARE requirements. Work closely with the Medical Directors in establishing evidence based clinical decisions. Responsible for clinical research necessary to establish clinical guidelines, create and update policy keys in the Clinical Decision Support tool, and perform research for the Technology Assessment Committee as assigned.

Sr. CRA

AZ regional/5 state regionAll therapeutic areas: CV, oncology, CNS—Alzheimer, ALS, depression; Thrombosis; Project leader for CV trials. Project liaison for ICH/Regulatory issues.Monitor and manage investigative centers for contracted sponsor’s Phase II through IV clinical drug and device trials. Responsible for total site management activities including qualifying potential investigators, initiating clinical sites, training study personnel, and performing interim study monitoring visits. Also responsible for monitoring study progress, data collection, protocol compliance, query resolution, preparing interim status reports, and conducting study closeout visits. Additional responsibilities include drug accountability, training new field monitors, developing monitoring tools for project use, assisting with site audit procedures, completing audit resolution activities, sponsor contact, and meeting presentations. Experienced in data entry systems.

Msn, Clinical Nurse Specialist In Cv Nursing

Bsn, Nursing

Activities and Societies: Sigma Theta Tau