Pharmacy Technologists (2)

Job Title: Pharmacy Technologist (2) Location: Rachuonyo, Homabay County Reports To: Site Pharmacist / Study Coordinator Position Type: Full-time, Contract Job Purpose: He/she will support the site pharmacist in receiving, storing, preparing, and dispensing investigational products (IP) in accordance with the study protocol, Good Clinical Practice (GCP), Good Pharmacy Practice (GPP), and sponsor guidelines.

The role requires meticulous documentation, strict adherence to blinding procedures, and close collaboration with the clinical team.

Key Responsibilities: Assist in the reception, storage, and inventory management of investigational product (MK-8527 and comparator). Help prepare and dispense IP to study participants per prescription and protocol.

Ensure accurate labeling, packaging, and documentation of dispensed products.

Maintain proper inventory logs and stock cards under the supervision of the site pharmacist.

Support reconciliation of returned medication and maintain accountability records.

Assist in documentation and reporting of temperature excursions or product discrepancies.

Provide participants with instructions on how to take the investigational product, emphasizing adherence and safety.

Collect and document returned pills/blisters during follow-up visits.

Report any observed adverse events or participant concerns to the pharmacist and clinical team.

Assist in the identification, documentation, and reporting of adverse drug reactions (ADRs) as part of pharmacovigilance responsibilities.

Support the management and accountability of non-investigational medications, including concomitant and supportive care medications.

Ensure proper storage, labeling, and dispensing of non-investigational medications in compliance with protocol and regulatory guidelines.

Maintain accurate records of pharmacovigilance data and safety reports under the supervision of the site pharmacist.

Ensure that investigational products are stored under required conditions (e.g., temperature-controlled environments). Monitor and record refrigerator/freezer temperatures as per protocol and SOPs.

Adhere to GPP, GCP, and blinding protocols in all pharmacy activities.

Collaborate closely with the pharmacist, study clinicians, and coordinators to ensure timely IP dispensing.

Assist with preparation for audits and monitor visits.

Maintain cleanliness and organization of the pharmacy area.

Qualifications & Experience: Must have minimum a Diploma in Pharmaceutical Technology from a recognized institution.

Valid registration and license from the Pharmacy and Poisons Board (PPB) or relevant national body.

Must have a minimum of 1 year of experience in a clinical or research setting (experience in clinical trials is an advantage). Must be trained in Good Clinical Practice/Good Pharmacy Practice principles and clinical research documentation.

Key Competencies: High attention to detail and accountability.

Strong organizational and record-keeping skills.

Ability to work discreetly and maintain participant confidentiality.

Good interpersonal and communication skills.

Comfortable working in a regulated, fast-paced research environment.

Working Conditions: Stationed in the on-site pharmacy or designated IP storage and dispensing area.

May involve working outside of routine hours to align with participant visit schedules.

Strict adherence to blinding, confidentiality, and safety protocols.

Applications must include the following: Application letter, Complete CV with 2 referees indicating their telephone contacts and e-mail contacts Relevant certificates and testimonials If qualified for the above post, please send your application addressed to the Principal Investigator, MK8527 Study.

If qualified for the above post, please send the above documents to the email by 27/7/2025 NB: Applications without the above-mentioned qualifications or required certificates will NOT be considered.

Only shortlisted candidates will be contacted.

Click on the link below and fill out the Google form.