Bioanalytical Scientist
Pharmaron

Germantown, Maryland

This job has expired.


Come Join Our Growing Team!

We are looking for a Bioanalytical Scientists to join our team in Germantown, MD. This role is responsible for carrying out laboratory and office-based tasks within stated timeframes and in accordance with Standard Operating Procedures (SOPs) and Company Policies. Contributes to the scientific research and application of 14C bioanalysis. Supports Sr. Scientist in method development and strives towards laboratory independence and leadership to junior lab staff. Maintain positive and professional working relationships with coworkers of all levels. This is a 100% on-site role based in Germantown, MD.

What The Job Entails:

  • Prepares data tables and reports within Laboratory Information Management Systems and custom Excel workbooks.
  • Provides support in obtaining reference materials, control matrices and project-specific consumables to meet the objectives of the study.
  • Participates in data transfers, pre-clinical and clinical data management tasks.
  • Assists in training personnel in the operation, maintenance, and troubleshooting of laboratory equipment.
  • May contribute to department initiatives, e.g. process improvements, as required.
  • Always complies with the Laboratory Safety Policy.
  • Always complies with company Standard Operating Procedures unless specifically varied in the validation or sample analysis plan.
  • Provides support in developing and validating LC+AMS and β-RAM/MicroBeta assays to detect 14C related material.
  • Supports organization of electronic and physical study file according to study templates and checklists in preparation of quality assurance review.
  • Supports draft study document management and review including phase plans, amendments, notes to file, reports, and others.
Requirements:
  • Master of Science in relevant field + at least 2 years relevant experience, OR Bachelor of Science in relevant field + at least 4 years relevant experience.
  • Good Laboratory Practice (GLP) regulations (21 CFR part 11 and 58)
  • Good Clinical Practice (GCP) regulations


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