We are looking to add a Study Director - ADME to our Drug Metabolism team in Madison, WI. Fully competent in a feeder role for a study director with skills and competencies in the relevant study types.

This position provides support for study abroad programs and international student services. This position advises students about approved study abroad programs, processes information and updates for international student visa support, and works with the Global Fairfield team to communicate appropriate information to students, parents, faculty and staff on internal procedures related to the development and implementation of application, admissions and communications procedures.

Serve as Study Director (or equivalent) for exploratory pharmacokinetic and toxicology studies in house, including working with project lead on study design, scheduling, test article receipt, protocol and report preparation.

Stain tissue samples using immunohistochemistry (IHC) techniques, score samples, generate reports detailing scoring data and experimental results for study sponsors (customers) The Histology Technologist contributes to our mission by supporting the Study Director throughout the duration of a project including sponsor and study director updates, developing study design, assisting with proposal writing, and presenting to clients.

Collecting, reviewing and approving of all required regulatory documents; and working to ensure the study Trial Master File (TMF) is up to date and “audit ready” throughout the course of the study.

Plan and execute, in conjunction with CCI Faculty Fellow for Global Engagement, all study abroad marketing and outreach efforts (i.e. Attend study abroad fair, plan and coordinate CCI information sessions, host workshops.

Clean and maintain assigned areas of lab by assisting with kennel and animal care as needed and communicating any animal health status issues to attending DVM and study director/sponsor. · May assist with acute and survival surgical procedures per protocol, and all clinical laboratory and radiographic procedures, under the direction of the attending DVM. · Maintain animal health throughout the study through consultation with DVM on diagnosis and treatment, administering prescribed therapy and monitoring response to treatment.

Assist with study related regulatory documents and ensure the Trial Master File (TMF) is up to date and audit ready throughout the course of the study. Collaborate with project investigators and research sites to ensure targets are met for study start up site activation patient recruitment and enrollment.

For GS-7: (A) one year of specialized experience equivalent to at least the GS-5 grade level OR (B) one full year of graduate level education with major study in business administration, public administration, agricultural economics (food industry management), or other fields related to the position; or superior academic achievement, OR (C) a combination of specialized experience and education.

Ensure that all appropriate regulations, procedures and data collection protocols are being followed throughout the course of a study and delay studies, if necessary, until manager and/or study director can be notified.

The Home Study and Post Release Worker (HSPRW) is responsible for conducting home studies of prospective sponsors and providing post release services to youth who have been released from ORR’s custody to a sponsor in the United States.

Primary manager of Don Bosco Cristo Rey (DBCR) Corporate Work Study Program in the CSO, as related to oversight, supervision, and productivity of four (4) students from DBCR. CSO liaison for the DBCR Corporate Work Study program manager, regarding billing, student assignments, and administrative details for CSO intern program.

This position requires an individual to be certified as a Child Study Team (CST) member (School Psychologist, LDT/C, Social Worker) in the State of New Jersey and Special Education Liaison or School Psychologist for New Jersey.

Performs non-invasive testing procedures to evaluate arterial and venous circulation using a hand held Doppler, pulse volume recorder, photo plethysmography and duplex ultrasound imaging techniques; Performs more complex studies such as post-op graft evaluation, renal artery Duplex study, AVF/AVG evaluation and Endovascular Duplex study.

As a Clinical Research Coordinator working at the Mesa (East Valley Chandler) site Monday - Friday you will be responsible for study coordination, including study start-up, patient recruitment, backup support, and other duties as required at the location.