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Investigational Pharmacist Jobs (NOW HIRING)

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 ...

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 ...

The investigational drug research pharmacist will interact with investigators, study sponsors, research colleagues and other healthcare providers. * You will create, monitor, document, and follow ...

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Investigational Pharmacist information

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How much do investigational pharmacist jobs pay per hour?

As of Aug 25, 2026, the average hourly pay for investigational pharmacist in the United States is $60.91, according to ZipRecruiter salary data. Most workers in this role earn between $56.01 and $67.31 per hour, depending on experience, location, and employer.

What does an investigational pharmacist do?

An Investigational Pharmacist specializes in managing medications used in clinical trials. They ensure investigational drugs are stored, prepared, and dispensed according to strict regulatory guidelines. They collaborate with researchers, monitor drug accountability, and ensure patient safety. Their role is critical in maintaining compliance with protocols and supporting the development of new therapies.

What are the typical responsibilities of an investigational pharmacist during a clinical trial?

As an Investigational Pharmacist, you play a critical role in ensuring the safe and compliant management of investigational medications throughout all stages of a clinical trial. Your day-to-day tasks involve drug preparation, labeling, storage, and dispensing according to study protocols, while maintaining rigorous documentation for regulatory purposes. You regularly collaborate with principal investigators, study coordinators, and sponsor representatives to address protocol requirements or resolve medication-related queries. The position demands a high level of accuracy and adherence to regulatory and ethical standards, making your contributions vital to the success and integrity of clinical research studies.

What are the key skills and qualifications needed to thrive as an investigational pharmacist?

To thrive as an Investigational Pharmacist, you need a solid background in pharmacy, thorough knowledge of clinical trial protocols, and a PharmD or equivalent degree, often with board certification. Familiarity with clinical trial management systems, electronic data capture (EDC) tools, and regulatory documentation is essential. Attention to detail, effective communication, and strong organizational skills help professionals excel in managing complex studies and working with multi-disciplinary teams. These competencies ensure safe handling of investigational drugs, regulatory compliance, and smooth collaboration across clinical research settings.

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What are the most commonly searched types of Investigational Pharmacist jobs?

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Infographic showing various Investigational Pharmacist job openings in the United States as of August 2026, with employment types broken down into 2% Internship, 3% As Needed, 67% Full Time, 26% Part Time, and 2% Contract. Highlights an 98% Physical, and 2% Remote job distribution, with an average salary of $126,701 per year, or $60.9 per hour.

Investigational Pharmacist

LCMC Health

New Orleans, LA • On-site

Other

Posted 4 days ago


LCMC Health rating

6.7

Company rating: 6.7 out of 10

Based on 128 frontline employees who took The Breakroom Quiz

531st of 893 rated healthcare providers


Job 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.

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About LCMC Health

Sourced by ZipRecruiter

LCMC Health, located in New Orleans, Louisiana, US, is a non-profit health system committed to providing high-quality healthcare services. Established in the year 2009, the company operates in the healthcare industry and dexterously manages several institutions, including children’s hospitals, academic medical centers, and local area hospitals. Employing over 8,500 skilled professionals across its network, LCMC Health's mission is to provide healthcare that goes beyond the ordinary to make a positive difference in every life it touches. Their core values encapsulate this mission too, prominently featuring care, innovation, trust, and respect.

Industry

Health care and social assistance

Company size

5,001 - 10,000 Employees

Headquarters location

New Orleans, LA, US

Year founded

2009

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