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Clinical Pharmacy Specialist

Employer
General Healthcare Resources
Location
Atlanta, Georgia, US
Closing date
Oct 7, 2021

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Position Type
Clinical Pharmacist
Specialty Area
Other
Work Setting
Health System
GHR Search is looking for Pharmacists with prior Clinical Trials or Clinical Research experience for a Remote/Work from Home ongoing contract.

A Pharmacy license from any state within the United States is acceptable for this assignment.

PLEASE NOTE: The office you will be working for is based on the East Coast , therefore hours will be coordinated with their office hours and needs.

· Full Time Hours with possible Overtime

· Hourly Rate: $60/hr

· Client will send you a company laptop and phone to use for completion of assignment

· Length of Assignment: Ongoing, no definitive end date.

Please see position information below. If you are interested, please submit your resume and we will reach out to you!

Job Requirements:

Job Responsibilities

· Reviews reports and maintains site specific trackers for enhanced monitoring of the unblinded IP handling activities

· Monitor usage of site inventory through reviews of study documentation, including but not limited to, IP shipment documents, inventory dashboards, IRT reports, data visualizations, preparation records, duties and investigational product accountability logs/forms

· Assess local site inventories to ensure adequate IP and ancillary supplies are available for the next two-days of scheduled participants

· Coordinates IP for predictive enrollment to ensure adequate supplies are available to complete the study design

· Provides support to ensure temperature excursion assessments are resolved in a timely manner

· Reviews dose preparation records and accountability logs daily to ensure the physical inventory accurately reflects the IP containers dispensed and there is adequate IP remaining for future vaccinations

· Reviews documents that are uploaded and filed in XXXXXX or a site's equivalent system that maintains the electronic Investigator Site File (eISF) and source documents (eSource) (e.g. unblinded source documents)

· Maintains effective and ongoing communication with investigator site, unblinded study team members (e.g. unblinded SPONSOR and XXXX Study Managers, unblinded CRAs and Site Care Partners, as needed), and appropriate SPONSOR Global Clinical Supply colleagues throughout the duration of the study

· Assist with overseeing the day to day unblinded IP handling activities of the study including problem solving, communication and IP management

· Responds to appropriate unblinded IP handling queries in consultation with Global Clinical Supply colleagues

· Completes all required IP handling training for the XXXXXX protocol

For additional questions please reach out to Rachel Riegel at 484-567-0730

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