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Research Pharmacist

Centre for Infectious Disease Research in Zambia Lusaka, Zambia

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Employer and vacancy source: Centre for Infectious Disease Research in Zambia

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  • EmployerCentre for Infectious Disease Research in Zambia
  • LocationLusaka, Zambia
  • Employer websitewww.cidrz.org
  • Application methodExternal application link
  • Listing sourceZambia Job Alerts
Job facts

Key details for this vacancy

Employer
Centre for Infectious Disease Research in Zambia
Location
Lusaka, Zambia
Posted
February 18, 2025
Job type
Full Time
Category
Other
Application method
External application link

Website Centre for Infectious Disease Research in Zambia

Job description

Job summary

Reports to Head Pharmaceutical Services, Investigators of Record. The incumbent is responsible for all pharmaceutical issues within the Clinical Research Sites.

Main duties

Establishes all necessary forms, policies and procedures to ensure the safe and proper use of all study products including the preparation of a Pharmacy Plan and Standard Operating Procedures for Drug Storage; Temperature Monitoring: Drug Access Protocol; Dispensing Protocol.
Adheres to Pharmaceutical Affairs Branch (PAB) Pharmacy Guidelines and Instructions for Division of AIDS (DAIDS) Clinical Trials Networks as well as institutional, local, regional, and country regulations.
Maintains the confidentiality of the participant, the participant’s pharmacy file, and the study product accountability record as well as maintain the blinding of the participant’s treatment assignment to investigators, study nurses, clinic staff and the participant.
Ensures that study products are dispensed only to eligible study participants and that participants have signed an informed consent before dispensing protocol-provided study products.
Ensures that study products are dispensed only after the written order of the Investigator of Record or upon the order of a licensed clinician directly responsible to the IoR
Maintains accurate records of receipt, control, dispensing and accountability of protocol provided study products and other drugs specific to the study. Including dates, quantities, lot numbers, use by participants, and amounts s returned or disposed of at the request of the Sponsor
Ensures adequate space, equipment, and supplies for the storage, preparation, packaging, and dispensing of study products including products that require special handling.
Ensures proper verification on the accountability records whenever protocol-provided study product supplies are returned, that all remaining supplies including returns from participants have been returned either to the Sponsor other source.

Qualifications

Degree in Pharmacy
Experience with management of drugs and related commodities
Knowledge of the MOH Healthcare system
Computer literate
Work with minimum supervision
3 years minimum years’ experience
Valid practicing license

Suitably qualified candidates are invited to apply. However, only shortlisted candidates will be contacted.

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