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Research Analyst I- Bioanalytical

Req ID #: 222898

Cleveland, Ohio, USA

About this job

We are seeking a Research Analyst I for our Bioanalytical Chemistry Team at our Safety Assessment site located in Cleveland, OH.

We are seeking a Research Analyst I for our Bioanalytical Chemistry Team at our Safety Assessment site located in Cleveland, OH.

Bioanalytical Chemistry supports the evaluations of test compounds by providing bioanalytical quantitative analysis of drug in body fluids and tissues from non-regulated and regulated studies including preclinical safety evaluations, pharmacokinetic/pharmacodynamic studies, and clinical trials. Staff participate in the development and validation of quantitative LC/MS/MS methodology, sample analysis, and interpretation and reporting of data utilizing validated hardware and software systems. This includes the development of sample extraction techniques, rapid LC separations, and employment of laboratory robotics to enhance delivery time of bioanalytical data. Staff are also knowledgeable in the application of GxP’s and applicable SOPs, along with adhering to study protocols to accurately document methods, procedures, and results for inclusion into study reports and regulatory documents.

Essential Functions (The fundamental Competencies/Skills & Responsibilities of the role (products and services provided/results accomplished) include, but are not limited to, those listed: 

  • Efficiently perform and document all procedures, materials and results in compliance with applicable regulatory standards as applicable (protocols, methods, SOPs, etc.)
  • Demonstrate effective communication skills through informal discussions with peers, supervisor, and team
  • Assist with laboratory maintenance functions
  • Independently perform laboratory support functions such as labeling and solution preparations
  • Assist with maintaining study specific inventory of consumables with oversight
  • Write both study and non-study deviations with minimal oversight
  • Actively participate in process improvement initiatives with oversight
  • Develop critical thinking, troubleshooting and time management skills aligned with needs of the operational area
  • Assist in execution of routine sample analysis studies with oversight
  • Assist in execution of method validation projects with oversight as needed
  • Operate laboratory instruments with complete oversight
  • Assist with data analysis in appropriate software for at least one analytical platform
  • Performs all other related duties as assigned

The starting pay for this position is $21.00/hr. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location

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About Charles River

Charles River is an early-stage Contact Research Organization (CRO). Here, we are passionate about our role in improving the quality of people's lives. With 100 sites around the globe, we are strategically positioned to coordinate worldwide resources and apply multidisciplinary perspectives in resolving our clients' unique challenges. Our client base includes global pharmaceutical companies, biotechnology companies, government agencies and hospitals and academic institutions around the world.

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