· Ensure that all study drugs are stored according to protocol/SOP/manufacturers instructions in restricted access area to prevent loss or use by unauthorized individuals.
· Maintain IP storage area visit log.
· Maintain pharmacy temperature conditions and continuous temperature monitoring: record the storage temperature and relative humidity twice daily, except for the days off.
· Report any deviation to the Pharmacist.
· Perform weekly uploads from the data logger records to an electronic device and USB key, and retain the printed version of data logger reports in the pharmacy site file.
· Assist with pharmacy quality assurance and quality control processes.
· Complete and maintain pharmacy records for the sponsor and regulatory audits.
· Assist monitors in drug accountability activities.
· Assist with procurement of trial medication.
· Receive trial drugs from suppliers; document receipt and resolve discrepancies.
· Maintain accurate and proper records for all drugs received and distributed by the trial pharmacy, according to trial SOPs.
· Prepare weekly medication blister packs for participants as per prescriptions from trial doctors, in accordance with trial SOP, under direct supervision of the trial pharmacist.
· Label trial medication before dispensing, in accordance with trial SOP, under supervision of the trial pharmacist.
· Dispense trial medication, as per specific protocol/SOP requirements, under the supervision of the trial pharmacist.
· Assist the treatment coordinator in counselling and educating patients on drug administration, side effect, and adherence under direct supervision of the trial pharmacist.
· Receive and reconcile IP returns.
· Assist with pill counts and adherence monitoring.
· Return and/or properly dispose of trial drugs as per protocol/SOP.
· Maintain stock control and a record of dispensed medication, according to trial SOPs.