Principal Pharmacist

First Job Previous Job 3,274 of 10,000 More Like This Salary Not Available Position range in Kansas City, MO-KS Metropolitan Statistical Area $131k•$163k Per Year Principal Pharmacist

MRIGLOBAL

Occupation:

Pharmacists

Location:

Kansas City, MO•64116

Job Type:

Full Time (30 Hours or More)

Posted:

05/01/2026 Positions available: 1

Source:

FileImport•

MRIGLOBAL

Web Site:

jobs.dayforcehcm.com

Expires:

06/30/2026 Job #: 5111 Job Requirements and Properties Help for Job Requirements and Properties. Opens a new window. Work Onsite Full Time Schedule Full Time Job Description Help for Job Description. Opens a new window. Are you passionate about making the world better? Are you looking for an organization that aligns with your values? MRIGlobal solves challenging problems through science, engineering, and program management. We are an independent scientific research organization dedicated to benefiting society and fostering a safe, healthy, and sustainable environment. When you embark on a career with MRIGlobal, you are joining a crew of world-class talent and problem solvers. Established in 1944, MRIGlobal is headquartered in Kansas City, MO, working in several states including Virginia and Maryland. Role Summary We are seeking a candidate with clinical research and investigational product experience to provide pharmacy leadership and Principal Investigator-level program leadership for government and commercial clinical trial programs. This individual will be embedded on-site within our existing cGMP clinical trial materials warehouse and will play a key role in: Supporting current programs Enabling new government contract bids Serving as the accountable Principal Investigator / Project Director for regulated clinical research support programs Serving as licensed pharmacy leadership for investigational products This is a programmatic, leadership-oriented position focused on clinical trials, regulatory compliance, quality systems, and operational execution across large, multi-site research programs. Primary Responsibilities Program & Contract Leadership Serve as Principal Investigator (PI) / Project Director with overall responsibility for execution of regulated government and commercial clinical research programs Provide licensed pharmacy oversight for investigational products used in clinical trials Support proposal development and capture activities for new government and commercial opportunities Act as a primary technical authority and subject matter expert during audits, site visits, inspections, and sponsor interactions Provide end-to-end leadership for program execution, including coordination with operations, quality, regulatory, and program management teams Clinical Trial Pharmacy & Investigational Product Oversight Oversee receipt, storage, labeling, packaging, and distribution of investigational products Ensure compliance with c

GMP, ICH, FDA

/ CFR, and Applicable state Boards of Pharmacy Support blinded study operations and investigational product accountability Provide cognitive pharmaceutical input (protocol review, pharmacy procedures, product handling, stability considerations) Operational, Quality & Cross-Functional Collaboration Work closely with staff, quality and regulatory teams, and scientific and program leadership Own and continuously improve pharmacy and investigational product quality systems, including SOP governance, audit readiness, and corrective/preventive actions Help maintain, govern, and evolve SOPs related to pharmacy operations and investigational product handling Support scaling activities if new contracts are awarded Minimum Qualifications PharmD from an accredited institution Active U.S. pharmacist license (state flexible; Missouri licensure preferred or obtainable) 5+ years of experience in one or more of the following: Clinical research pharmacy, Investigational drug services (IDS), Clinical trial supply management, CRO, CDMO, or government-adjacent contractor environment Demonstrated experience with investigational products in clinical trials Familiarity with regulatory frameworks governing clinical trial materials (cGMP, ICH, FDA) Demonstrated ability to provide program-level leadership in regulated clinical research environments Preferred Qualifications Experience supporting NIH, NCI, NIAID, or other federal programs Experience with: Blinded studies, international shipment of clinical trial ...For full information see follow application link.