IDS Clinical Pharmacist Specialist

Summary

Investigational Drug Services (IDS) pharmacist specialist is involved in the drug distribution process related to investigational medications utilized in clinical trials. The IDS clinical specialist is involved in clinical trial start up including performing feasibilities and facilitating creation/maintenance of standardized treatment order sets within Cerner Medication Integration (PowerChart/ PharmNet). Reviewing IDS fee schedule and reconciling Assists in reviewing, updating and developing policies and procedures in accordance with institutional and regulatory requirements. The IDS Clinical Specialist assists Moffitt Primary Investigators in protocol and pharmacy manual development.IDS clinical specialist actively participates in research study clinical activities, in order to ensure safe and effective use of investigational medications in accordance with the Code of Federal Regulations (CFR) and Good Clinical Practice (GCP) guidelines. IDS clinical activities include but are not limited to: assist in clinical trial initiation, protocol review/adherence, order set development/maintenance, drug distribution activities, hazardous/non-hazardous compounding, and collaboration with clinical research team to provide complex comprehensive care to research patients.

Salary Range

$145,308.80 - $221,603.20

Salary ranges posted for this position represent the expected base pay range for the role. Actual compensation may vary based on location and a variety of job-related factors, including experience, skills, education, and internal equity among Team Members in similar positions.

We are committed to maintaining fair and equitable pay practices and regularly review compensation to ensure alignment across our workforce.

Moffitt Career Site

Requirements

Bachelor's Degree in Pharmacy; Licensed Pharmacist (RPh/ PS); CITI Certification (GCP, human subjects research, conflicts of interest) or Board Certified Oncology Pharmacist (BCOP) OR PGY2 graduating residents must obtain BPS Certification within 12 months of hire date (external new hires) or transfer date (internal team members) into position. Incumbent will be considered to be compliant if they have sat for the exam within the 12-month timeframe and passed the exam. Certification indicating successful exam pass must be provided to Moffitt within 90-days following the date of the test sit date. Should incumbent not meet this requirement, consideration for a move to a position not requiring the above certification may be considered.; Minimum of 4 years progressive institutional oncology pharmaceutical experience or PGY-1 with 2 years progressive institutional oncology pharmaceutical experience or PGY-2/Advanced Pharmacy Practice Residency/Ph.D. in related field; Proficient in the drug distribution process as it relates to clinical trial process.; Clinical practice skills in patient assessment, pharmacology, genomics, supportive care, and personalized medicine applications.; Excellent skills with communications, research, writing, computer applications, group dynamics and supervision.