Key Responsibilities

• Performing high complexity testing according to established SOPs for molecular
  diagnostic techniques, including nucleic acid extraction, PCR, genotyping, and
  next generation sequencing.
• Correctly receiving, requisitioning, processing, and ensuring proper identification
  of specimens and chain of custody.
• Setting up, validating and performing maintenance checks on laboratory
  equipment and automation solutions.
• Managing laboratory supplies and inventory for smooth laboratory operations.
• Participating in reagent and assay quality control and validations.
• Participating in internal and external quality assurance programs.
• Troubleshooting assays and instruments as needed.
• Maintaining strict quality standards according to laboratory accreditation standards, e.g. CAP, CLIA, ISO.
• Preparing for internal/external audits as needed.

Key Responsibilities:

• Tracking the delivery of, receiving, and checking patient specimens against order forms.
• Accessioning specimens into the laboratory information management system (LIMS) to facilitate sample throughput.
• Performing specimen processing under the direct and constant supervision of a licensed CLS.
• Performing routine laboratory maintenance tasks such as instrument calibration and maintenance.
• Maintaining an adequate level of supplies for the laboratory, which includes tasks such as ordering, receiving, unpacking, documentation and labeling of consumables and reagents, and stocking work areas.
• Participating in quality control and quality assurance activities as relevant.
• Performing any other administrative tasks to facilitate smooth clinical operations.

Key Responsibilities

• Receiving and checking specimens (including COVID-19 specimens), sorting and labeling patient samples, and preparing them for data entry and analysis in accordance with the Standard Operating Procedures (SOPs) and safety requirements of the laboratory.
• Supporting the laboratory in the area of pre-processing.
• Following all laboratory protocols and policies in checking the quantity of specimens received and ensuring that specimen identification tallies with the request forms.
• Ensuring and assisting in the care, cleanliness and maintenance of the laboratory work area and equipment.
• Maintaining an adequate level of laboratory supplies in the work area, receiving requested stock items and distributing them to the appropriate places within the laboratory.
• Performing administrative and clerical tasks, as well as inventory management or other assigned duties (e.g. freezer defrosting).
• Assisting medical laboratory technologists/lab staff during the laboratory tests when required (e.g. contamination monitoring).
• Assisting in ensuring smooth logistics and workflow of international deliveries of specimens to our laboratory. This would involve identifying packaging and delivery requirements for specimens from overseas markets (e.g. the US) and tracking of delivery status.
• Specimens are received at our laboratory for cancer diagnostics and COVID-19 testing. Please note that you will not be coming into direct contact with any of the specimens, but you should be comfortable handling the kits, blood tubes etc. that contain such specimens. These would include blood/tissue samples for cancer-related tests and swab/saliva samples for COVID-19 tests. You will be required to do personal protective equipment to handle COVID-19 specimens.

Key Responsibilities:

• Processing specimens (including Covid-19 specimens) and performing high complexity testing according to established SOPs for molecular diagnostic techniques, including nucleic acid extraction, polymerase chain reaction, genotyping, and next generation sequencing.
• Analyzing data and reporting results accurately following established procedures and with the strictest adherence to safety procedures.
• Troubleshooting and resolving technical problems.
• Conducting technical and clinical verification and validation studies.
• Participating in internal and external quality assurance programs.
• Monitoring inventory and lab supplies in assigned areas.
• Performing other duties as assigned to ensure smooth laboratory operations.

Key responsibilities:

• Facilitating the coordination of clinical research activities between the relevant internal teams, the clinical research organization and study sites. Day-to-day responsibilities include writing and reviewing of study documentation, trial monitoring, data management, logistical arrangements, site initiation and patient enrollment, and stakeholder coordination to ensure study timelines and goals are met.
• Providing support and managing queries from both internal and external stakeholders, including study sites, for the smooth execution of clinical studies.
• Identifying, troubleshooting and mitigating possible barriers that may adversely affect our clinical studies.
• Leading process improvements for more efficient execution.
• Assisting in any other relevant matters that facilitate the company’s clinical development pipeline.

Key Responsibilities

• Based on an in-depth understanding of Lucence’s technology and product portfolio and medical science, interpreting genomic alterations in appropriate clinical contexts and reporting results accurately and timely following established procedures.
• Working closely with the Medical Data Science team in the curation and maintenance of database – evaluating scientific publications/clinical studies and integrating functional effects of genomic variants and their associated diseases using standard terminologies and established guidelines.
• Writing, maintaining and updating workflows and protocols for clinical reporting pipeline.
• Participating in research-oriented projects for clinical validation of tests (in collaboration with external organizations).
• Participating in internal and external quality assurance programs.
• Performing other relevant duties as assigned.

Key Responsibilities

• Planning and conducting experiments in collaboration with fellow Lucence staff and relevant partners.
• Organizing data and interpreting results from experiments.
• Troubleshooting experimental and/or instrumental issues.
• Designing improvements to the microfluidic devices being tested.
• Develop prototypes to translate wet-lab procedures into easy-to-use platforms.
• Fabrication of microfluidic chips and consumables for experimental work.
• Supporting laboratory organization and maintenance, such as sourcing and preparation of materials and calibration and maintenance of instruments.
• Liaising with external partners in research collaboration projects.

Key Responsibilities

• Planning and conducting experiments in collaboration with fellow Lucence staff and relevant partners.
• Organizing data and interpreting results from experiments.
• Troubleshooting experimental and/or instrumental issues.
• Designing improvements to the optical and imaging systems being tested.
• Supporting laboratory organization and maintenance, such as sourcing and preparation of materials and calibration and maintenance of instruments.