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Operational Data AnalystApply Now

Location: Lexington, Massachusetts
Employment Type: Contract

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Job Description

Contract Length:  6 months; hybrid schedule

Job Summary:  This position is responsible for the quality control of all non-GLP data generated in the Nonclinical Pharmacology group.

Responsibilities:
 
  • Work closely with scientists within the ADME group to verify bioanalytical data generated using HPLC-FD and LC-MS/MS.
  • Work closely with scientists within the in-vivo pharmacology group to verify in-vivo and Pharmacodynamic (qPCR) data.
  • Review and verify all data to ensure accuracy, completeness, and compliance with internal guidelines and acceptance criteria.
  • Generate reports/checklist for all QC findings, along with subsequent discussions with relevant scientists in order to resolve issues.
Requirements:
 
  • Familiarity with analytical software
  • Familiarity with regulatory guidelines and standards related to bioanalytical data review.
  • Excellent communication and collaboration skills.
  • Prior experience in quality control of Scientific data.
  • Minimum of 1 year experience with data review/QC
  • Education:  A degree in a relevant scientific discipline, such as Biochemistry, Biotechnology, Pharmacology, or related fields

Contact

Rob Wallace
Principal Recruiter

Rob works on the Contract team. His goal as a recruiter is to continue to establish long-term professional and personal relationships with top-performing HR professionals throughout the Greater Boston area.


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