Project Scientist

For 75 years, Charles River employees have worked together to assist in the discovery, development and safe manufacture of new drug therapies. When you join our family, you will have a significant impact on the health and well-being of people across the globe. Whether your background is in life sciences, finance, IT, sales or another area, your skills will play an important role in the work we perform.

In return, we’ll help you build a career that you can feel passionate about.

The BioA LBA discipline support large molecule drug development using ligand binding assays (LBA), such as enzyme-linked immunosorbent assay, to measure large molecules and their immune responses. The main types of assays include Pharmacokinetic assays to measure drug and Immunogenicity assay to measure anti-drug antibodies and neutralizing antibodies. Other assay types also performed are branched DNA and cell-based assays.

• Effectively manage a portfolio of sample analysis projects while ensuring timelines are met in a single operational area with oversight.
• Execute review and approval of data with oversight for final scientific/technical decisions within a single operational area.
• Develop understanding of compliance expectations to respond to quality assurance audit observations in appropriate software with oversight.
• Assist with oversight the completion of laboratory investigations, assay troubleshooting and quality observations.
• Assist in problem solving for technical and/or regulatory issues with oversight.
• Responsible for writing and preparing study plans/protocols/amendments with minimal oversight.
• Participate in Sponsor visits/tours with minimal oversight.
• Develop expertise in developing and validating quantitative/qualitative methods/procedures with limited complexity/scope in one operational area with minimal oversight.
• Perform data analysis using appropriate software with minimal oversight.
• Develop critical thinking, troubleshooting and time management skills aligned with needs of operational areas.
• Demonstrate effective communication skills through informal discussions with peers, supervisor, and team.
• Function as a liaison, maintaining timely and frequent communication between CRL and Sponsor/Client/SD with minimal oversight.
• Ensure scientific integrity of studies with minimal oversight.
• Function as a Principal Investigator, Individual Scientist and/or Study Director as assigned with minimal oversight.
• Actively communicate and collaborate across operational areas in order to adhere to timelines and produce quality data.
• Efficiently perform and document all procedures, materials and results in compliance with applicable regulatory standards as applicable (protocols, methods, SOPs, etc.).
• Write, review and approve deviations with oversight.
• Develop knowledge of regulatory and GXP requirements, industry standards and company SOPs within one operational area.
• Effectively manage a small portfolio of research projects including method development and validation while ensuring timelines are met in a single operational area with oversight.
• Performs all other related duties as assigned.

• Bachelor’s degree (BA/BS) with 5-7 years of relevant working experience. Master’s degree (MS) with 1-2 years of relevant work experience. Doctorate degree (PhD) with no experience.
• Ability to communicate verbally and in writing at all levels inside and outside the organization.
• Basic familiarity with Microsoft Office Suite.
• Computer skills, commensurate with Essential Functions, including the ability to learn a validated system.
• Ability to work extended hours beyond normal work schedule to include, but not limited to evenings, weekends, extended shifts, and/or extra shifts, sometimes on…