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Laboratory Support Manager-Mycobacteriology


This is a Contract position in Los Angeles County, CA posted May 14, 2019.

Responsibilities The Laboratory Support Manager (LSM), with supervision from the management team, for Mycobacteriology Research functions as a collaborator for HIV and TB research in support of clinical studies sponsored by the Division of AIDS (DAIDS) / National Institute of Allergy and Infectious Disease (NIAID) / National Institutes of Health (NIH).

The employee will play a role in the implementation of mycobacteriology/TB-centric clinical trials protocols, information management and Network organization and structure.

The LSM is responsible for reviewing and implementing protocol testing, reviewing laboratory quality assurance information, working with laboratories to resolve audit/monitoring visit findings and supporting capabilities required to conduct clinical trials as required by the protocol Sponsor.

The LSM also provides committee coordination and administrative support to laboratory related committees and working groups.

Qualifications Familiarity with both classic and molecular TB screening and diagnostic and drug susceptibility testing methods, including laboratory QA/QC processes.

Have a working knowledge of recent CDC and WHO guidelines for laboratory testing and diagnosis of TB disease.

Knowledge or experience with other infectious diseases such as HIV/ADIS, preferred.

Familiar with laboratory methods, and technologies used to screen and diagnose LTBI, TB and MDR/XDR-TB.

The LSM must have a thorough understanding of Good Laboratory Practices and /or CLIA/CAP requirements.

The LSM is responsible for knowledge related to the performance of complex laboratory procedures.

In addition, the LSM should be able to: recognize deviations from expected and/or normal results; analyze results for possible solutions; recommend new test methodologies and/or modify existing ones to achieve desired results; evaluate new laboratory techniques; prepare and analyze a variety of data; provide detailed documentation and analysis of clinical research data.

The LSM should be able to: organize and direct the daily activities of participating laboratories; participate with supervisor in work planning, staff training, evaluating work, and counseling; evaluate quality control procedures; review work of others for conformance with quality control procedures; maintain quality control records; perform safety checks; ensure compliance with health and safety guidelines.

Ability to develop and provide instruction and training for staff at international laboratories in performance of laboratory procedures including total quality management.

Ability to develop, with assistance, necessary training tools to assist laboratories (i.e., checklists, training materials, etc.).

Working knowledge of assay validation, quality assurance and quality control procedures and properly documenting laboratory processes and procedures as well as corrective and preventative actions (CAPA) plans.

Excellent interpersonal and client management skills with a professional and customer service oriented demeanor.

Excellent verbal and written communications skills, which may include business and technical writing, editing and proofreading.

Experience working with laboratory data/information management systems or laboratory database would be beneficial.

Possess at least a Bachelor’s (BS) degree in science field or Medical Technologist.

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