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Job Descrption

The QASMC Laboratory is dedicated to formally evaluate the mechanisms of inflammation in general and specifically in respiratory disease (asthma, allergy, COPD). The clinical trials unit conducts clinical studies to evaluate and determine the potential of new therapeutic agents in asthma, allergy and COPD, and also in urology and gastro-enterology. The clinical research facility manages clinical trials from Phase II-IV. The unit has consolidated its expertise and experience and has a proven track record in performing clinically based pharmacological research to the highest international standards.

We require a Laboratory Technician to join the research team within the specialised clinical trials laboratory. The technician will crucial role in supporting clinical trials by handling biological samples, conducting tests, and ensuring the accuracy of data. Their responsibilities are essential for the integrity of the research.

KEY RESPONSIBILITIES

To proactively perform pre-analytical... processing of biological samples following the applicable Policies, Standard Operating Procedures (SOPs) and GCP/GCLP guidelines.

To maintain, update and develop study data documentation and administrative tasks.

To be able to collect, label, and store biological samples (e.g., blood, tissue, urine) from clinical trial participants.

Ensure proper handling, processing, and preservation of samples to maintain integrity and prevent contamination.

Follow protocols for sample transportation, including cold chain management.

Perform routine and specialised laboratory tests on collected samples as per study protocols.

Operate and maintain laboratory equipment, such as centrifuges, microscopes, fridges and freezers and consumables.

Ensure accuracy and precision in measurements and results

Accurately record data from tests and observations in databases and required documentation

Adhere to quality standards, control and assurance to maintain the integrity of research

EXPERIENCE

Experience of working in a laboratory environment, minimum of 1 year, preferably under GCP/GCLP standards.

Experience of working in a clinical research setting is desired.

Accuracy in documentation of data and effective time management skills.

Good computer and communication skills.

Experience of non-supervised lab activities. The post holder will be expected to operate with minimal supervision in organising and planning their own work activities.

EDUCATION

BSc Health Sciences or equivalent experience.

SCHEDULE

Mon- Fri 08:00-17:00

Please, note: The salary will be depending on experience.

Job Type: Full-time

Pay: £25,000.00-£31,000.00 per year

Schedule:
• Monday to Friday

Work Location: In person

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