Job Description & Requirements
- Work closely with the local departments, and adapt to changing priorities with guidance from senior team members.
- Work with specimens maintained at varying temperatures (ranging from ambient to cryogenic), including the limited movement of shipper boxes filled with dry ice.
- Perform receipt, QC checks, labeling and onward processing of clinical trials specimens.
- Specimens Accessioning: Perform accurate data entry into various laboratory information management systems
- Specimen Storage: maintain full inventory and tracking of storage specimens while ensuring the integrity of the specimens at all times
- Specimen Shipping and Disposals: prepare specimens for real-time and scheduled onward shipment to other referral laboratories. Process specimens marked for disposal.
- Raise and resolve specimen management-related queries with other departments.
- Perform housekeeping to maintain a clean and tidy working environment, including basic freezer maintenance and disposition of waste.
- Support monitoring of cold storage units and environment.
- Utilise study documentation to aid in problem solving and escalate to senior staff as required.
- Manage specimen-related study documentation including archiving
- Monitor and maintain consumables inventory.
- Perform all processes in accordance with SOPs and appropriate regulatory guidelines including Good Clinical Practices (GCP) and IATA
- Perform other duties as assigned
Requirements:
- Minimum Higher Nitec or Diploma in arelated field
- Excellent communication skills
- Exceptional documentation and data entryskills
- 5-day work week including Saturday
- Willing to learn, positive attitude and mustbe a team player
- Trained in IATA Dangerous GoodsRegulations (DGR) would be advantageous
- Salary will commensurate with experience