Clinical Research Pharmacist

Tennessee Oncology • Nashville, TN

22h • Onsite

About The Position

Tennessee Oncology, a large, community-based cancer care specialist with a leading clinical trial network, is seeking a Clinical Research Pharmacist. This role is responsible for providing clinical resources to clinical trial patients, research staff, and pharmacy staff. The position ensures compliance with all regulatory requirements for medication-related components of clinical trial protocols, maintains pharmacy product quality, and oversees the preparation and dispensing of investigational products. The Clinical Research Pharmacist also provides clinical support and oversight for delegated pharmacy personnel, offers drug information, patient education, and supports professional staff. The mission of Tennessee Oncology is to provide access to high-quality cancer care and clinical research expertise to all patients in convenient community locations.

Requirements

• Doctor of Pharmacy (PharmD) or Bachelor’s Degree in Pharmacy (BS Pharm)
• Successful completion of a PGY1 and/or PGY2 residency specializing in oncology or 3 years of clinical pharmacy/IDS experience
• Current, active, and unrestricted Tennessee Pharmacy licensure
• Proven presentation experience
• Possess the personal characteristics of professionalism, credibility, commitment to high standards, and innovation
• Adept to continual learning and development
• Effective communication skills including patient education, staff mentoring and drug information to the extended health care team
• Self-starter with the ability to work independently and within a team
• Accomplished in team building and management
• Ability to change between tasks with accuracy and proficiency
• Knowledge and compliance of regulatory bodies that apply to IDS

Responsibilities

• Serve as coordinator/liaison between research and pharmacy departments for all clinical trial needs
• Participate in feasibility assessment, protocol review, and site initiation visit (SIV) for all clinical trials
• Provide 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)
• Serve as the training and regulatory point of contact for all delegated pharmacy personnel, including providing ongoing training to pharmacy staff when needed
• Maintain study pharmacy manuals and/or protocols in pharmacy shared drive for pharmacy staff reference
• Communicate with sponsor study monitors and respond to all pharmacy-related inquiries in a timely manner
• Maintain inventory of investigational products in designated storage locations
• Dispense investigational product(s) for all clinical trial patients; research coordinators will provide additional coverage if needed
• Act as the primary pharmacy contact for all research-related pharmacy questions
• Collaborate with research and pharmacy departments to create interdepartmental standard operating procedures (SOPs)
• Assure the appropriateness of medication therapy (investigational and commercial) through review and completion of medication reconciliation for clinical trial patients during screening and on an as needed basis
• Review of medication orders for clinical appropriateness based on patients’ specific conditions and concomitant therapies
• Compound and accurately dispense intravenous solutions and related supplies
• Formulate, prepare, and maintain quality control of pharmaceutical preparations
• Check medication preparation and oversee delegated pharmacy services performed by pharmacy technicians
• Communicate with prescribers and providers regarding appropriateness of drug therapy and patient response to therapy
• Build and update treatment regimens in EMR for all clinical trial protocols
• Fulfill responsibilities listed in various pharmacist job descriptions on an as-needed basis (e.g., critically low staffing levels)
• Function as a team member by expanding the responsibilities as directed by management to facilitate optimal workflow within the cancer center
• Completes expected competencies as defined by manager
• Serve on various committees, as requested, as expert resource for IDS
• Miscellaneous duties as assigned requested and/or required

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level