Oncology Clinical Research Pharmacist

Florida Cancer Specialists•Florida - Remote, FL

1d•Remote

About The Position

The Oncology Clinical Research Pharmacist will serve as a member of the central services team where our focus is to deliver best in class pharmaceutical support to all clinical staff throughout the organization. As a member of the Pharmacy Operations team, the incumbent will ensure delivery of therapeutic medication monitoring, EMR regimen build and review, protocol management, medication information, and education that ensures safe and effective medication therapy for patients enrolled in a clinical trial/research regimen. Under the supervision of the Director of Pharmacy Operations, the Oncology Clinical Research Pharmacist (OCRP) works collaboratively with all Research Department staff (i.e., physicians, coordinators, regulatory affairs, pharmacy, nursing, lab, and ancillary personnel, and others) to provide quality patient care appropriate for the patient’s oncologic diagnosis, prescribed treatment, age group and other identified needs. Duties and responsibilities include providing drug information, dosing, monitoring, and education to ensure accurate and efficient delivery of investigational medication(s); coordinating, collaborating, and providing expertise in support of clinical trials; performing administrative and communication responsibilities; supporting the development of new research regimen builds and inquiries; and performing other duties consistent with the job classification, as required. Demonstrates working knowledge of all facets of role, relevant regulations, and organizational and departmental policies and procedures. Performs other duties and projects as assigned. Performs all duties in accordance with regulatory requirements and organizational policies and procedures.

Requirements

Registered Pharmacist in the State of Florida.
Valid state Driver’s License for travel to satellite offices and offsite meetings.
Compliance with the company Driver Safety Operations and Motor Vehicle Records Check Policy is required.
Minimum of 5 years’ experience as a clinical pharmacist working in a hospital, home health, community oncology, or other infusion center.
Critical thinking skills including solid problem solving, analysis, decision-making, planning, time management and organizational skills.
Must be detailed oriented with the ability to exercise independent judgment.
Ability to follow complex instructions, master basic math skills, work with interruptions and deadlines.
Strong interpersonal skills.
Ability to effectively communicate and interact with coworkers, hospital staff, patients, sponsor representatives, public, physicians and staff, in a calm and friendly manner.
Developed interpersonal skills, emotional intelligence, diplomacy, tact, conflict management, delegation skills, and diversity awareness.
Ability to work effectively with sensitive and confidential material and sometimes emotionally charged matters.
Good command of the English language.
Effective communication skills (oral, written, presentation), active listener, and effectively provides balanced feedback.
Able to communicate well on the phone.
Strong customer focus.
Ability to build an engaging culture of quality, performance effectiveness and operational excellence through best practices, strong business and political acumen, collaboration and partnerships, as well as a positive employee, physician, and community relations.
Effectively lead and facilitate group discussions, coach, mentor, motivate, and engage others to align to a common goal.
Ability to effectively lead projects from inception through implementation and assessment.
Effectively manages own time, conflicting priorities, self, stress, and professional development.
Self-motivated and self-starter with ability work independently with limited supervision.
Ability to work remotely effectively as required.
Able to work autonomously.
Must be able to work effectively in a fast-paced, multi-site environment with demonstrated ability to juggle competing priorities and demands from a variety of stakeholders and sites.
Must be able to enter and retrieve data from computer, operate modern office machinery, including the phone system.
Proficiency in Microsoft Office: Word, Excel, PowerPoint, and Outlook preferred.

Nice To Haves

Board Certification in Oncology (BCOP) preferred.
2 years of experience in a research-related field preferred.

Responsibilities

Provide drug information, dosing, monitoring, and education to ensure accurate and efficient delivery of investigational medication(s).
Coordinate, collaborate, and provide expertise in support of clinical trials.
Perform administrative and communication responsibilities.
Support the development of new research regimen builds and inquiries.
Perform other duties consistent with the job classification, as required.
Demonstrate working knowledge of all facets of role, relevant regulations, and organizational and departmental policies and procedures.
Perform other duties and projects as assigned.
Perform all duties in accordance with regulatory requirements and organizational policies and procedures.