Key Responsibilities:

Administer respective Case Report Forms (CRFs)
Carrying out QA/QC of study CRFs and source docs and resolve queries that may arise.
Dispensing drugs and Study products to participants.
Ensure prescription drugs are available for dispensing to participants
Maintaining pharmacy temperature and humidity logs
Develop and review of pharmacy SOPs and ensuring adherence to the same
Counselling participants on adherence to study products
Participants Randomization process in liaison with the data and clinic teams.
Maintain the pharmacy database and keeping it up to date.
Ensuring accurate and timely records of dispensed drugs and study products on the pharmacy logs and in the accountability logs and Database.
Processing shipment documentation of study products and track study product shipment from source to site.
Processing study products destruction documents and taking part in actual destruction process.
Enhancing communication between pharmacy and local PPB and coordinating Center.
Management of regulatory affairs regarding pharmacy and the study.

Vacancy Requirements:

Diploma in Pharmaceutical Technology    Mandatory
Registered with the Pharmacy and Poisons Board    Mandatory
Good Clinical Practice or Human Subjects Protection training will be an added advantage    Added Advantage
Commitment to integrity and high-quality performance    Mandatory
Good interpersonal skills and ability to work in a team    Mandatory
Keen and attentive to detail    Mandatory
Good communication skills    Mandatory
Counselling skills    Mandatory
Computer literacy    Mandatory