IDS Clinical Pharmacist Specialist

Moffitt-Cancer-Cente; Tampa (FL); On-site; USD 145,000 - 222,000; Full time

Job summary

Moffitt Cancer Center in Tampa, FL seeks an Investigational Drug Services (IDS) Pharmacist Specialist to oversee drug distribution for investigational medications used in clinical trials and to participate in trial start-up, feasibility, and creation/maintenance of standardized order sets within Cerner PowerChart/PharmNet.

The IDS clinical specialist assists investigators with protocol and pharmacy manual development.

Qualifications

• Bachelor's Degree in Pharmacy required.
• Licensed Pharmacist (RPh/PS) required.
• CITI Certification (GCP, human subjects research, conflicts of interest) or BCOP; PGY2 residents must obtain BPS within 12 months of hire.
• Excellent communications and research skills.

Responsibilities

• Oversee drug distribution for investigational medications in clinical trials.
• Assist in clinical trial start-up, feasibility, and protocol development.
• Develop/maintain standardized order sets within Cerner PowerChart/PharmNet.
• Review IDS fee schedule and ensure regulatory compliance.
• Collaborate with the clinical research team to provide complex patient care in line with CFR and GCP.

Skills

Licensed Pharmacist

GCP/CITI Certification

Clinical trial coordination

Communication skills

Education

Bachelor's Degree in Pharmacy

Tools

Cerner PowerChart/PharmNet

Job description

Working at Moffitt is both a career and a mission: to contribute to the prevention and cure of cancer.As the only National Cancer Institute-designated Comprehensive Cancer Center based in Florida, Moffitt employs some of the best and brightest minds from around the world. Join a dedicated team of nearly 11,000 who are shaping the future we envision. Moffitt has been recognized as a Best and Brightest Company to Work For in the Nation and is continually named one of the Tampa Bay Times’ Top Workplaces.SummaryInvestigational 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.Minimum Requirements:Bachelor's Degree in PharmacyLicensed 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 fieldTraining Required: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.Salary Range$145,308.80 - $221,603.20Salary 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 SiteIf you have the vision, passion, and dedication to contribute to our mission,then we have a place for you!1. Equal Employment OpportunityMoffitt Cancer Center is an Equal Opportunity/Affirmative Action Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, or protected veteran or disabled status. We seek candidates whose skills, and personal and professional experience, have prepared them to contribute to our commitment to diversity and excellence.2. Reasonable AccommodationFederal law requires employers to provide reasonable accommodation to qualified individuals with disabilities. Please tell us if you require a reasonable accommodation to apply for a job or to perform your job. Examples of reasonable accommodation include making a change to the application process or work procedures, providing documents in an alternate format, using a sign language interpreter, or using specialized equipment. Moffitt endeavors to make moffitt.org/careers accessible to any and all users. If you would like to contact us regarding the accessibility of our website or need assistance completing the application process, please contact one of the Human Resources receptionists by phone at 813-745-7899 or by email at [e-mail]. This contact information is for accommodation requests only and cannot be used to inquire about the status of applications.Read more information about your EEO rights under the law.Transparency in Coverage Rule