Laboratory Technologists (2)

Job Title: Laboratory Technologist (2) Location: Rachuonyo, Homabay County Reports To: Laboratory Manager / Study Coordinator Position Type: Full-time, Contract Job Purpose: He/she will be responsible for performing study-specific laboratory procedures including the collection, processing, analysis, and shipment of biological samples as outlined in the study protocol.

The technologist will ensure adherence to Good Clinical Laboratory Practice (GCLP), biosafety standards, and sponsor guidelines, contributing to the accuracy and reliability of trial data.

Key Responsibilities: Receive, label, and process participant blood, urine, and other biological specimens according to study protocol.

Perform centrifugation, aliquoting, and storage procedures as per sponsor SOPs.

Ensure proper documentation and tracking of all specimens using sample tracking logs and systems.

Record all results accurately in laboratory records and case report forms (CRFs). Maintain logs for equipment usage, maintenance, temperature monitoring, and quality control.

Follow standard operating procedures (SOPs) and Good Clinical Laboratory Practices (GCLP). Implement daily quality control checks and troubleshoot any testing issues.

Ensure biosafety measures and waste disposal procedures are strictly followed.

Operate and maintain laboratory equipment (e.g., centrifuges, refrigerators, pipettes). Perform daily equipment checks and escalate any malfunction or maintenance needs.

Monitor lab consumables and inform the lab manager when stock is low.

Store samples in appropriate freezers/fridges with correct labeling and logging.

Prepare and package samples for shipment to central/reference laboratories following IATA guidelines.

Maintain proper chain of custody and documentation for all shipped specimens.

Qualifications & Experience: Must have minimum, a Diploma in Medical Laboratory Sciences or equivalent.

Must be registered and licensed by a recognized body (e.g., KMLTTB in Kenya). Must have at least 2 years of experience in a clinical or research laboratory (experience in clinical trials is an added advantage). Training or experience in GCLP and biosafety procedures.

Key Competencies: High attention to detail and accuracy in specimen handling.

Strong organizational and record-keeping skills.

Good communication and teamwork abilities.

Familiarity with sample tracking and basic data entry systems.

Ability to work effectively under pressure and meet Flexibility to work early mornings, evenings, or weekends as needed by study demands.

Working Conditions: Lab-based position with strict adherence to biosafety and confidentiality protocols.

May involve early morning or evening work to accommodate study visit schedules.

Occasional travel for training or courier sample drop-off, if required.

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.