Lead Research Analyst, Chemistry Bioanalysis

Charles River Laboratories

Shrewsbury (MA)

Sur place

USD 37 000 - 40 000

Plein temps

Il y a 20 heures
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Avantages offerts par ce poste

Bonus/incentives based on performance
401K
Paid time off
Stock purchase program
Health and wellness coverage
Employee and family wellbeing support

Résumé du poste

Charles River Laboratories is seeking an experienced Research Analyst II to serve as lead technician for multiple studies, developing and performing laboratory procedures while guiding less experienced staff. The role emphasizes GLP-compliant data collection, coordination of study activities, and collaboration with scientific teams.

Responsibilities include overseeing study notebooks, data documentation, and ensuring adherence to SOPs and study protocols.

Qualifications

  • Bachelor’s degree in a laboratory science or related discipline is required.
  • Two to four years of related experience in biology, chemistry/pharmacy, or similar lab environment, or equivalent combination of education and experience.
  • Knowledge of GLPs and working with data collection equipment is expected.

Responsabilités

  • Lead technician on assigned studies, coordinating study procedures.
  • Review peers' activities and documentation for study compliance.
  • Prepare, conduct, and oversee technical activities with scientific staff.
  • Manage study timelines and resources with supervision.

Connaissances

Mentorship
Team collaboration
Attention to detail
GLP knowledge

Formation

Bachelor’s degree in laboratory science or related discipline

Outils

MS/LC-MS equipment

Description du poste

Charles River Laboratories is seeking an experienced Research Analyst II to serve as lead technician for multiple studies, developing and performing laboratory procedures while guiding less experienced staff. The role emphasizes GLP-compliant data collection, coordination of study activities, and collaboration with scientific teams.

Responsibilities include overseeing study notebooks, data documentation, and ensuring adherence to SOPs and study protocols.

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