Senior Scientist, Bioanalytical - Small Molecule CRO - Idaho

Idaho, Idaho Permanent USD100,000 - USD130,000 per year
  • Design & optimize bioanalytical methods for the analysis of pharma compounds.
  • Join fast paced/growing Contract Research Organization (CRO).

About Our Client

My client is a Contract Research Organization (CRO) that provides comprehensive services to pharmaceutical and biotech companies throughout the drug development process primarily with small molecules. They offer a range of services, including analytical and bioanalytical testing, drug discovery, preclinical studies, and late phase clinical trials. They have a team of highly skilled and experienced professionals who are committed to delivering high-quality services to their clients. They have a great company culture and built a collaborative environment where everyone works towards common goals. My client also built a brand new state of the art lab facility.

Job Description

As a Senior Scientist, you will play a crucial role in our bioanalytical services team. You will be responsible for method development, method validation, analysis of samples supporting drug development. The ideal candidate will have a strong background in CRO bioanalytical sciences, exceptional analytical skills, and a passion for contributing to the advancement of pharmaceutical and biotech research.

  • Method Development and Validation: Design and optimize bioanalytical methods for the analysis of pharmaceutical compounds in various biological/chemical matrices. Conduct method validation in accordance with regulatory guidelines.
  • Sample Analysis: Perform sample analysis using a variety of analytical techniques, ensuring accuracy and precision in the measurement of drug compounds and metabolites.
  • Documentation and Compliance: Generate comprehensive plans, data, reports, and other documentation to support drug development studies. Ensure all activities are conducted in compliance with relevant procedures, industry standards, and regulations.
  • Collaboration: Work closely with cross-functional teams to support drug discovery, preclinical studies, and late-phase clinical trials. Collaborate with internal and external stakeholders to ensure successful project outcomes.
  • Quality Assurance: Maintain a high standard of quality assurance in all aspects of bioanalytical testing. Implement and adhere to quality control measures to meet or exceed industry standards.

MPI does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity or expression, national origin, age, disability, veteran status, marital status, or based on an individual's status in any group or class protected by applicable federal, state or local law. MPI encourages applications from minorities, women, the disabled, protected veterans and all other qualified applicants.

The Successful Applicant

  • Ph.D. or equivalent in a relevant scientific discipline (Chemistry, Biochemistry, Pharmacology, or related field).
  • 2+ years of direct CRO experience
  • Proven experience in bioanalytical method development and validation within a pharmaceutical or CRO setting.
  • Strong knowledge of regulatory guidelines (GLP/ICH, FDA, EMA, etc.) governing bioanalytical testing.
  • Proficiency in analytical techniques such as LC-MS/MS, HPLC, and other relevant technologies.
  • Excellent communication skills with the ability to effectively collaborate in a team-oriented environment.
  • Detail-oriented, with a commitment to producing high-quality and accurate results.

What's on Offer

  • Competitive base salary
  • Great benefits package
  • Amazing company culture
  • Fast paced/dynamic environment
  • Report directly to Laboratory Director
  • Work in brand new state of the are lab space
  • Relocation assistance when necessary
  • Ample growth opportunities
Grace Mcgrady
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Job summary

Life Sciences
Sub Sector
Healthcare / Pharmaceutical
Contract Type
Consultant name
Grace Mcgrady
Job Reference