Clinical Research Pharmacist

Celerion•Tempe, AZ

13d

About The Position

Celerion is committed to swift, exceptional clinical research through translational medicine. Every day, we use our experience, agility, and innovative research strategies to help get drugs to market faster. Track, prepare, and account for all investigational products. Act as a resource for study teams by utilizing pharmacological expertise and knowledge of pharmacy practice. Please note: Registered Pharmacist required .

Requirements

Registered Pharmacist required
Proven pharmaceutical experience of minimum 1-2 years
Proven record keeping skills with extreme attention to detail
Knowledge of United States Pharmacopeia guidelines, including chapters 795, 797, 800, 1163, and 1168 as well as the FDA Guidance for Industry CGMP for Phase 1 Investigational Drugs required
Completion of media bi-annual media fill and fingertip testing (as applicable per site)
Job-specific training is required and will be provided
Requires flexible work hours, namely for occasional on-call weekend availability

Nice To Haves

Doctor of Pharmacy preferred but not required
Knowledge of FDA and EU regulations preferred (if appropriate)

Responsibilities

Responsible for receipt, storage, preparation, disposition, and retention of all study investigational products in compliance with standard operating procedures, FDA, and DEA regulations concerning investigational product handling, accountability and security.
Review and understand study protocol requirements in regard to investigational product handling.
Active member of study team providing expertise and support such as evaluating study feasibility, study set up and conduct, participating in internal and/or external client meetings.
Provide internal and/or external client communication and interaction regarding investigational product handling and protocol specific requirements.
Knowledge of relevant United States Pharmacopeia guidelines, including chapters 795, 797, 800, 1163, and 1168 as well as the FDA Guidance for Industry CGMP for Phase 1 Investigational Drugs required.
Maintain aseptic compounding evaluation requirements.
Provide training and monitoring for administration of investigational products as needed.
Review and provide input to standard operating procedures and training plans pertaining to pharmacy and assisting with pharmacy training as necessary.
Maintain pharmacy department equipment and applicable records as necessary.
Institutional Review Board consultant and resource.
Assist in training of new hires and students.
Work with the Pharmacist in Charge to: o Ensure compliance with current USP guidelines and applicable Celerion SOP’s pertaining to extemporaneous pharmacy compounding Review applicable compounding SOP’s every 12 months to ensure continued compliance with USP guidelines and implement changes, as appropriate Ensure the CAPA system is initiated when warranted Oversee pharmacy personnel compounding training program Oversee compliance with USP guidelines Oversee monitoring of the Designated Compounding Areas Review and maintain all pharmacy compounding certification records (personnel and facility) to ensure completeness and compliance Recognize problems, deviations, failures, and errors in the compounding process and the facility and report all issues to the Pharmacist in Charge