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Clinical Trials Sample Management Technician I

ACM GLOBAL CENTRAL LABORATORY (SINGAPORE) PTE. LTD.

Singapore

On-site

SGD 20,000 - 60,000

Full time

Yesterday
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Job summary

A clinical laboratory company in Singapore is looking for a dedicated individual to manage clinical trials specimens, which includes tasks like labeling, QC checks, and data entry. The ideal candidate should possess a Minimum Higher Nitec or Diploma in a related field, excellent communication skills, and be a team player willing to learn. The position involves a 5-day work week and adherence to Good Clinical Practices (GCP). Competitive salary will be offered based on experience.

Qualifications

  • Minimum Higher Nitec or Diploma in a related field.
  • 5-day work week including Saturday.
  • Willing to learn, positive attitude and must be a team player.

Responsibilities

  • Work closely with local departments and adapt to changing priorities.
  • Perform receipt, QC checks, labeling and onward processing of clinical trials specimens.
  • Maintain full inventory and tracking of storage specimens.

Skills

Excellent communication skills
Exceptional documentation and data entry skills
Team player

Education

Minimum Higher Nitec or Diploma in a related field
Job description
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 elevate 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 a related field
  • Excellent communication skills
  • Exceptional documentation and data entry skills
  • 5-day work week including Saturday
  • Willing to learn, positive attitude and must be a team player
  • Trained in IATA Dangerous GoodsRegulations (DGR) would be advantageous
  • Salary will commensurate with experience
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