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McKenzie Davis
Healthcare Recruiter at Tennessee Oncology
Clinical Research Pharmacist is responsible for providing clinical resources to clinical trial patients, research department staff, and pharmacy department staff. Assures local, state, national, and federal regulatory compliance for all medication-related components of clinical trial protocols. Assures pharmacy product quality and compliance with legal pharmacy standards. Oversees delegated pharmacist and pharmacy technicians in the preparation of sterile IV admixtures of investigational products and dispensing of oral investigational products. Provides clinical support and oversight for delegated staff pharmacists and pharmacy technicians for all clinical trial protocols. Provides clinical pharmacy services though drug information, patient education, and to the professional staff. Lead the Oncology Drug Regimen Team (ODRT) with research builds.
ESSENTIAL FUNCTIONS:
as coordinator/liaison between research and pharmacy departments for all clinical trial needs
in feasibility assessment, protocol review, and site initiation visit (SIV) for all clinical trials
enhanced oversight for all double-blind clinical trials, including serving as primary un-blinded pharmacist, pharmacy binder maintenance, drug preparation, receipt, destruction, and data entry (when applicable)
as the training and regulatory point of contact for all delegated pharmacy personnel, including providing ongoing training to pharmacy staff when needed
study pharmacy manuals and/or protocols in pharmacy shared drive for pharmacy staff reference
with sponsor study monitors and respond to all pharmacy-related inquiries in a timely manner
inventory of investigational products in designated storage locations
investigational product(s) for all clinical trial patients; research coordinators will provide additional coverage if needed
contacts for all research-related pharmacy questions (questions from site staff, pharmacists, research team)
with research and pharmacy departments to create interdepartmental standard operating procedures (SOPs)
the appropriateness of medication therapy (investigational and commercial) through:
and complete medication reconciliation for clinical trial patients during screening and on an as needed basis
of medication orders for clinical appropriateness based on patients’ specific conditions and concomitant therapies
and accurately dispense, intravenous solutions and related supplies
prepare, and maintain quality control of pharmaceutical preparations
medication preparation and oversee delegated pharmacy services performed by pharmacy technicians
with prescribers and providers regarding appropriateness of drug therapy and patient response to therapy
and update treatment regimens in EMR for all clinical trial protocols
responsibilities listed in various pharmacist job descriptions on an as-needed basis (e.g., critically low staffing levels)
as a team member by expanding the responsibilities as directed by management to facilitate optimal workflow within the cancer center
expected competencies as defined by manager
on various committees, as requested, as expert resource for IDS
Introduction: My name is Pres. Lawanda Wiegand, I am a inquisitive, helpful, glamorous, cheerful, open, clever, innocent person who loves writing and wants to share my knowledge and understanding with you.
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