Laboratory Technologist

The International Centre for Reproductive Health (ICRH) Kenya is an independent organization established in 2000. We deal with many aspects under the wide umbrella of 'Reproductive Health', including Mother and Child Health and Sexual Health.

Role Overview

The Laboratory Technologist will be responsible for processing and testing study samples, maintaining high-quality standards, and ensuring compliance with clinical research protocols and Good Clinical Laboratory Practice (GCLP). The role involves managing laboratory data, equipment, and supplies while adhering to biosafety and ethical guidelines to support the implementation of study procedures.

Duties & Responsibilities

Sample Processing

• Verify labels and the quality of specimens collected.
• Process and prepare samples for laboratory testing and storage.
• Ensure proper packaging, storage, and transportation of samples to designated laboratories where applicable.
• Maintain sample integrity through adherence to specimen handling and cold chain requirements.

Laboratory Testing

• Conduct diagnostic testing of study samples using the investigational devices.
• Perform quality control procedures and ensure all tests are conducted according to SOPs and manufacturer guidelines.
• Ensure accurate recording and timely reporting of laboratory test results.

Quality Assurance and Compliance

• Ensure laboratory activities comply with Good Clinical Laboratory Practice (GCLP) and study protocols.
• Participate in internal and external quality assurance programs.
• Maintain proper laboratory documentation, logs, and records.
• Ensure adherence to biosafety and infection prevention procedures.

Data Management and Documentation

• Record laboratory results accurately in the electronic data capture systems.
• Maintain laboratory registers, specimen tracking logs, and inventory records.
• Support monitoring visits, audits, and inspections by ensuring all laboratory documentation is complete and accessible.

Equipment and Supplies Management

• Ensure proper use, calibration, and maintenance of laboratory equipment.
• Monitor stock levels of laboratory reagents, consumables, and supplies.
• Report equipment malfunctions and coordinate maintenance when necessary.

Coordination with Study Team

• Work closely with the laboratory team, clinicians, study coordinators, and data teams to ensure smooth implementation of study procedures.
• Participate in study meetings, trainings, and protocol updates.
• Support participant follow-up for repeat sample collection where required.

Biosafety and Ethical Compliance

• Adhere to laboratory biosafety standards and infection control procedures.
• Ensure confidentiality and ethical handling of participant samples and data.
• Follow national laboratory guidelines and institutional research policies.

How to Apply

Interested and qualified candidates should go to the International Centre for Reproductive Health careers portal at careers.icrhk.org to apply or use the application link provided: Apply Now.