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Research Analyst I, Disc Bioanalytical

Req ID #: 222687

Mattawan, Michigan, USA

About this job

We are seeking a Research Analyst 1 for our Discovery Bioanalytical Chemistry Team in Mattawan MI.

We are seeking a Research Analyst 1 for our Discovery Bioanalytical Chemistry Team in Mattawan MI.

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.

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

Operates applicable laboratory equipment, including any respective software applications, to prepare samples and/or solutions and quantitate sample runs.
Preparation of sample out of different biological matrices for analysis per applicable analytical methods and SOPs.
Communicates effectively with supervisors, colleagues, Principal Investigators, and Study Directors.
Demonstrates commitment to quality.
Effectively works in a team and demonstrates a commitment to achieving company goals.
Efficiently prioritizes assigned daily workload and uses time productively.
Punctual and reliable attendance according to MPI Research company policy.
Adheres to safety procedures at all times.
Reads, understands, and follows SOPs, safety requirements, regulatory guidelines, and company policies.
Consistently follows established methods for isolating and quantifying compounds for routine sample analysis utilizing standard analytical and immunology platforms.
Possesses the ability to execute validation studies under direction.
Consistently documents all procedures and materials in compliance with GxP standards.
Operates applicable laboratory instruments including their respective software applications to prepare sample and quantitate sample runs.
Possesses the ability to learn and utilize software applications.
Assists in the completion of laboratory investigations, assay troubleshooting, and quality observations, as needed.
Possesses a willingness to perform additional work as assigned by management and as part of the individual’s development plan.

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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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