Pharmacy RN

CenExel•Murray, UT

6d•$36 - $39•Onsite

About The Position

Coordinates and collaborates with the Pharmacist in providing support of clinical investigational drug trials; provide accurate and efficient dispensing of medication and performs cross-functional duties as required. May act as a resource to other staff with pharmacy-related questions.

Requirements

Must be able to effectively communicate verbally and in writing.
Clinical Research experience or currently licensed nurse without any disciplinary action.
Good Interpersonal skills, demonstrated through interactions with sponsor representatives, staff and subjects.
Reflect the professional image of the company, upholding the company’s vision in actions, demeanor, and appearance.
Must be self-motivated and able to perform tasks independently.
Capable of performing IP and Pharmacy tasks relevant to licensure and/or training.

Responsibilities

Reads and understands all study protocol and pharmacy manual requirements regarding the management of study drug and pharmacy related tasks.
Reviews protocols and investigator’s brochures or other additional information supplied by the Principal Investigator and the study sponsor for clinical investigational drug trials as required.
Ensures access to all studies. This may include IWRS/IVRS, IRT, SBIR, this may vary by protocol.
Monitors pharmacy activities on a daily basis to ensure adherence to study protocols and dispensing procedures.
Prepares and dispenses investigational drugs in accordance with the IRB-approved protocols.
Attends training for new studies to ensure IP/Pharmacy management is thoroughly understood and executed.
Organizes all important communication regarding IP and file in each individual study IP binder.
Ensures all IP logs are accurate and up to date.
Monitors visits by reviewing all confirmation letters to ensure the IP records are up-to-date and accurate; reviewing all follow up letters to ensure all action items are addressed before next visit; reviewing the site calendar to prepare for all monitor visits; and scheduling monitoring visits.
Assists with study in-services and other training as needed. This may also apply to off-site studies.
Ensures IP team has signed all study related logs.
Maintains detailed record of controlled medication and daily count at each shift change with re-order if needed.
Reviews source documents for accuracy and request changes, as needed.
Ensures the appropriate storage of investigational drugs according to the protocol and FDA guidelines.
Monitors temperature of pharmacy storage areas and report any temperature deviations of study drug to sponsor.
Communicates with the study team any discrepancies/violations noted during pharmacy procedures.
Attends sponsor Investigator’s meetings, site initiations, web/teleconferences and staff meetings as needed.
Supports and ensures strictest adherence to best practices, FDA Code of Federal Regulations, ICH (International Conference on Harmonization), GCP (Good Clinical Practices), CenExel standard operating procedures, site working Practices, protocol, and company guidelines and policies.
Assumes other duties and responsibilities as assigned. The above responsibilities are a general description of the level and nature of the work assigned to this classification and are not to be considered as all inclusive.