Scientific Association, Toxicology

at  Charles River Laboratories

Req ID #: 222424
Location:Reno, NV, US, 89511
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.

JOB SUMMARY

• The pay range for this position is $65,000.00 USD per year. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

BASIC SUMMARY:

Responsible for overseeing study conduct of preclinical efficacy and/or toxicology studies assigned by TFM within safety assessment. Responsible for protocols/study plans, coordinate with technical teams to allow appropriate execution of the study, including establishing study schedules, ensuring adequate Standard Operating Procedures are available and adhered to, oversees adequate data recording and reporting, and ensure regulatory requirements/expectations are met for the assigned study(ies). Overall interpretation of preclinical toxicity studies, evaluation and preparation of reports from the data collected during these studies, communication with sponsor representatives, initiating contact with potential clients will be required, Familiarity with study costs and impact of changes will be required. May be involved with development of new technologies/procedures.

QUALIFICATIONS:

• Education: Minimum of a Bachelor’s degree (BA/BS) or equivalent in Toxicology, Pharmacology, or related discipline. Prefer Master’s (MA/MS), Doctorate (PhD), PharmD, DVM, or MD degree or equivalent.
• Experience: 3-5 years related experience in a laboratory or scientific research environment. This position requires analytical thinking skills and a good understanding of scientific processes.
• An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.
• Certification/Licensure: None
• Other: Knowledge of Good Laboratory Practice (GLP) regulations. Familiar with scientific protocols and reports and all components required for completeness. Computer skills including MS Office software and database management. Working knowledge of Provantis and Business Objects systems. Strong organizational skills and attention to detail. Knowledge of medical terminology.

• Function as an independent Study Director in accordance with the applicable Good Laboratory Practices (GLPs).
• Designs, writes, reviews and edits, as necessary, Study Plans, amendments and study schedules that define and schedule all study activities.
• Oversees and coordinates all aspects of study procedures, whether performed within the department or by service departments.
• Ensures that projects are performed according to Standard Operating Procedures and Good Laboratory Practice regulations and is aware of appropriate regulations, guidelines and guidance’s.
• Writes, reviews and edits, as necessary, draft or final reports that document all study related procedures and results.
• Prompt verbal or written communication with Sponsors on study related business.
• Understands regulations and GLP’s as they relate to primary area of focus.
• Understands the study process from proposal to report.
• Oversees and coordinates study conduct (protocol development, technical guidance, and reporting).
• Assists in study planning, scheduling, and execution under the supervision of Sr. Scientist(s)/Scientific Manager.
• Host client visits and telephone/video conferences with support/guidance from Sr. Scientist(s) as needed.
• Effectively communicates with internal and external clients in a manner that generates confidence and builds trust.
• Works on studies/programs of basic complexity.
• Basic knowledge of Quality Assurance (QA)/Quality Control (QC) process Interacts with veterinary staff, understands the IACUC process, and understands the Study Director role in animal welfare.
• Gains familiarity with overall project costs and communicates with the technical supervisor as well as the Scientific Manager on issues of staffing and equipment. May attend scientific meetings, conferences and training courses to enhance job and professional skills.