Ordering of study drug -this involves ordering of study drug from the Clinical Research Products Management Centre (CRPMC)
Receipt of Study Drug- this involves checking the integrity of the goods supplied, reporting on the status of the temperature logger for when the study drug is in transit and verifying the quantities and the expiry dates of the study drugs
Destruction of study drug- this includes quarantine of study drug according to batch and quantity.
Pre-mark syringes and preparation of participant packs for scheduled study visits
Communication/advising problematic patients and liaising with the necessary staff regarding adherence and counseling
Verification of "Inform consent" document before study drug dispensation by placing a copy of signature page in pharmacy participant files
Quality management which entails quality control of the entire dispensing process till the participant receives study drug
Updating of SOP's and other documents as processes are changed
Maintenance of Pharmacy Equipment - includes servicing/calibration of temperature devices etc. according to the SOP in place
Dispensing of all medication to patients/participants
Keep up to date statistics of patients that receive drug on a daily basis
Maintaining of Shock boxes in the doctors consulting rooms
Preparation for the monitoring visit which includes quality control of all pharmacy procedures/documentation
Keep a record of all communication between sponsor and site
Desired Experience & Qualification
A Batchelor's degree in Pharmacy,
Registered with South African Pharmacy council.
2-3 years' experience in similar role.
Clinical trials experience will be advantageous
Job Types: Contract, PermanentSalary: From R23,000.00 per monthExperience:
in similar role: 3 years (Required)
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