- Location
- UMC - 2000 Canal St., United States of America
- Type
- Full-time
- Source
- Workday
Description
Your job is more than a job.
Responsible for implementing hospital and/or service line goals within the area. Performs other duties as assigned.
GENERAL DUTIES
- Performing day-to-day dispensing and accountability activities with regard to IRB-approved clinical trials.
- Establishing internal policies and procedures for developing and maintaining an Investigational Drug management system, which includes technical procedures for product ordering, adequate and safe receipt, handling, storage, dispensing, retrieval of unused product from subjects or researchers, and disposition of Investigational Medications (including documentation thereof).
- Consulting with University Medical Center New Orleans Research Staff to support research during the planning phase of investigator-initiated and sponsored clinical trials research, including but not limited to: (a) serving as a resource to Research Staff for issues of protocol budgeting, pharmacy reimbursement and patient flow logistics; (b) serving as a resource to Research Staff for issues of pharmacy relations with sponsors; and (c) serving as a resource to the IRB.
- Maintain a system for the inventory, distribution and dispensing of medications used in IRB-approved clinic trial research conducted under the auspices of University Medical Center New Orleans’s IRB. This includes receiving, accountability, inventorying, and returning/destroying all medications furnished under an IRB-approved protocol.
- For clinical trials where the PI controls the Investigational Drug at UMC, as approved by the IRB pursuant to a project-specific management plan, consult with the PI and Research Staff to ensure compliance with protocol and regulatory specifications for dispensing and, as requested by the IRB, to conduct audits of dispensing activity to the extent that such dispensing occurs through an IRB-approved management plan.
- Integrate scheduling of research therapy into standard treatment regimens for IRB-approved clinical trials, as appropriate.
- Maintain an archive of current and previous research protocols, manuals of procedures, and research informed consent and prescriptions for subjects at UMC.
- Prepare protocol-mandated records and reports on drug utilization and inventory.
- Participate in all site visits and audits at UMC as required by the FDA, OHRP, sponsors, regulatory or credentialing bodies.
- Prepare industry- or government-supplied pharmaceuticals (including medications where a UMC employee holds the IND for the Drug being tested) for administration to subjects at UMC per a University Medical Center New Orleans IRB-approved protocol.
- Obtain copies of adverse drug reactions documented and supplied by investigators or staff for subjects/patients receiving sponsor-supplied Investigational Drug or where a UMC employee holds the IND for the Drug being tested.
- Ensures adequate staff coverage for assigned department areas according to projected patient load and established budget.
- Monitors the day-to-day operations of assigned department staff, reacting effectively and efficiently to unplanned circumstances, demands and challenges facing the department to ensure consistent quality of service.
- Demonstrates expertise in hospital and department processes and keeps staff updated by remaining current with hospital and department guidelines, federal, state, regulatory & other governing policies, procedures or guidelines.
- Coordinates the departmental staff performance and improvement process, including the preparation, analysis and submission of required reports.
- Updates and improves the department processes and workflows.
- Participates as requested on teams, committees, and special projects, both internal and external, relating to investigation services.
- Functions as a staff pharmacist as workload and personnel shortages require.
EXPERIENCE QUALIFICATIONS
Minimum of 3 year’s post-graduate pharmacist experience in institutional pharmacy preferred; preferably 3 or more years of progressive responsibility. Experience in research-based activities preferred.
LICENSES AND CERTIFICATIONS
Louisiana licensed pharmacist or eligible.
WORK SHIFT:
Days (United States of America)LCMC Health is a community.
Our people make health happen. While our NOLA roots run deep, our branches are the vessels that carry our mission of bringing the best possible care to every person and parish in Louisiana and beyond and put a little more heart and soul into healthcare along the way. Celebrating authenticity, originality, equity, inclusion and a little “come on in” attitude is the foundation of LCMC Health’s culture of everyday extraordinary
About University Medical Center
University Medical Center, a world class academic medical center in LCMC Health’s incredible community of care, is the largest medical training center for healthcare professionals in Louisiana and has long served as the region’s safety net hospital for poor and underserved communities for 300+. Learn more about University Medical Center’s legacy and our vision of becoming the epicenter of medical care, education, and research.
Your extras
- Deliver healthcare with heart.
- Give people a reason to smile.
- Put a little love in your work.
- Be honest and real, but with compassion.
- Bring some lagniappe into everything you do.
- Forget one-size-fits-all, think one-of-a-kind care.
- See opportunities, not problems – it’s all about perspective.
- Cheerlead ideas, differences, and each other.
- Love what makes you, you - because we do
You are welcome here.
LCMC Health is an equal opportunity employer. All qualified applicants receive consideration for employment without regard to race, color, religion, sex, national origin, sexual orientation, gender identity, disability status, protected veteran status, or any other characteristic protected by law.
The above job summary is intended to describe the general nature and level of the work being performed by people assigned to this work. This is not an exhaustive list of all duties and responsibilities. LCMC Health reserves the right to amend and change responsibilities to meet organizational needs as necessary.
Simple things make the difference.
1. To get started, take your time to fully and accurately complete the application for employment. Incomplete applications get bogged down and are often eliminated due to missing information.
2. To ensure quality care and service, we may use information on your application to verify your previous employment and background.
3. To keep our career applications up-to-date, applications are inactive after 6 months and, therefore, require a new application for employment to be completed.
4. To expedite the hiring process, proof of citizenship or immigration status will be required to verify your lawful right to work in the United States.