Key Responsibilities:


Dispense investigational products, compounded medicines, and concomitant medications per protocol and Standard Operating Procedures
Maintain accurate participant/patient medication records in compliance with Good Clinical Practice
Order, receive, and reconcile pharmaceutical and clinical trial supplies
Ensure proper custody, storage, and accountability of study drugs and related supplies
Maintain a compliant, audit-ready, and organized pharmacy environment
Support the development and implementation of study-specific Standard Operating Procedures and pharmacy documentation
Conduct quality checks on investigational medicinal products, including physical inspections and verifying packaging integrity.
Report any discrepancies, deviations, or adverse events related to investigational medicinal products handling.
Manage the return or destruction of unused or expired investigational medicinal products according to regulatory guidelines and trial protocols.
Perform other pharmacy-related duties as assigned by the Investigator or Clinical Research Scientist


Vacancy Requirements:


Diploma in Pharmaceutical Technology or its equivalent from a recognized institution;    Mandatory
Registration Certificate issued by the Pharmacy and Poisons board;    Mandatory
Proficiency in computer application; and    Mandatory
3 years of relevant experience in clinical research.    Mandatory
Communication Skills    Mandatory
Interpersonal Skills    Mandatory
Team player    Mandatory