Biosample Associate

San Francisco, CA 94158

Posted: 06/29/2020 Employment Type: Contract Industry: R&D Job Number: 7930

Job Description


Our client is a clinical-stage biopharma company developing a pipeline of drug candidates which are designed to improve the benefits of drugs for patients. The product pipeline consists of drug candidates across a number of therapeutic areas, including oncology, pain, anti-infectives and anti-viral and immunology. R&D development activities involve small molecule drugs, peptides and other potential biologic drug candidates.


Duties:
  • This position is located in the Bioanalytical Sample Management group and will support the sample management and bioanalysis for clinical trials.
  • Candidate will be responsible primarily for management of clinical samples using Laboratory Information Management System (LIMS), and organizing clinical samples and freezer spaces.


Skills: 
  • Responsible for receiving, organizing, and transferring clinical samples using LIMS. 
  • Working closely with internal and external groups/vendors to provide oversight of clinical sample management and to identify and resolve sample-related issues.
  • Maintaining accurate internal sample databases.
  • Participating in internal/external audits.
  • Must be able to maintain accurate and well-organized sample records, worksheets and electronic notebooks.


Education:
  • A bachelor’ s degree in a scientific discipline.
  • 2 years’ work experience in a regulated (GCP, GLP, or GMP) or development (bioanalytical, QC) environment is desired.

Job Requirements

Skills: 

  • Responsible for receiving, organizing, and transferring clinical samples using LIMS. 
  • Working closely with internal and external groups/vendors to provide oversight of clinical sample management and to identify and resolve sample-related issues.
  • Maintaining accurate internal sample databases.
  • Participating in internal/external audits.
  • Must be able to maintain accurate and well-organized sample records, worksheets and electronic notebooks.


Education:

  • A bachelor’s degree in a scientific discipline.
  • 2 years’ work experience in a regulated (GCP, GLP, or GMP) or development (bioanalytical, QC) environment is desired.
Apply Online
Apply with LinkedIn Apply with Facebook Apply with Twitter

Send an email reminder to:

Share This Job:

Related Jobs:

Login to save this search and get notified of similar positions.