Pharmacy Coordinator (RN)

Centricity Research•Columbus, OH

6d•Onsite

About The Position

We’re looking for a full-time Pharmacy Coordinator (RN) to support the efficient and accurate conduct of clinical trials under the direction of Research Management. In this role, you will play a critical part in ensuring the safe and compliant handling of investigational products (IP) and other medications, while supporting the clinical team and delivering exemplary patient care. You will be responsible for maintaining accurate records and ensuring that all pharmacy operations meet regulatory and protocol standards for both blinded and unblinded studies. This is a fully on-site position in our Columbus, OH office.

Requirements

You are licensed as a Registered Nurse in the state of Ohio.
You have at least 1 year of hospital or pharmacy experience and are comfortable working with medications in a regulated environment.
You are detail-oriented, organized, and committed to maintaining accurate documentation and drug accountability.
You are familiar with or eager to learn clinical trial procedures, including storage, labeling, documentation, and regulatory compliance.
You communicate clearly and work well with clinical teams, sponsors, CROs, and external partners.
You are committed to exemplary patient care and understand the importance of precision in medication handling in clinical research.
You are proactive, responsible, and able to manage day-to-day workflow with minimal oversight.
You are interested in supporting continuous improvement and helping train others as needed.

Responsibilities

Prepare, dispense and administer medications under the direction of a pharmacist or physician.
Maintain and inspect expiration dates for all IP, medications, and supplies required for pharmacy use.
Maintain accurate drug accountability logs for all medications, including oral and injectable formulations.
Ensure drug accountability logs are up-to-date by the end of each business day.
Maintain proper storage and security conditions for all drugs according to protocol requirements.
Monitor and record temperatures for ambient rooms, refrigerators, and freezers.
Establish and maintain patient drug administration records for Sponsors, CROs, regulatory agencies, or other industry representatives.
Follow protocol-established procedures for each clinical trial, including labeling vials or bottles with subject information.
Renew DEA license and Pharmacy license as required.
Establish and maintain professional working relationships with Sponsors, CROs, and other industry representatives.
Ensure the availability of documents, records, and used/unused drugs for monitoring visits (blinded or unblinded).
Support accurate completion of Case Report Forms (CRFs) and Electronic Data Capture at site level.
Follow procedures for drug destruction at trial close-out, as outlined by Sponsor or CRO.
Train staff and model continuous improvement practices within the pharmacy team.
Assist with other duties as needed based on study and site needs.