- Interacts with veterinary staff, and thoroughly understands the IACUC process and the Study Director role in animal welfare.
- Proactively provides developmental support, coaching, and/or assistance to other team members.
- May review reports of peers.
- Understands Charles River capabilities and identifies opportunities for cross selling; assumes a significant role in cross-selling to clients, acting as part of a team that involves other disciplines.
- Recognizes gaps and opportunities for improvements by keeping current with "State of the Art" techniques/procedures and assist in effectively transferring this information to and/or provides training to build intellectual capital within the corporation.
- Has direct impact on profitable revenue generation.
- May participate in the proposal management and bid development process.
- Collaborates on strategies and tactics for obtaining new business.
- Seeks ways to improve the delivery of products and services.
- Presents collaborative or independent research internally or externally; may publish data and/or scientific methodology in scientific publications. May participate in co-travel with commercial operations.
- Maintains involvement in various departmental/divisional projects and/or committees.
- Education: Bachelor's (BSc), Master's (MA/MSc), Doctorate (PhD), PharmD, DVM, or MD degree or equivalent in Toxicology, Pharmacology, or a related discipline.
- Experience: Generally 8 to 10 years related industry experience.
- 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
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Senior Research Scientist - Reno, United States - Charles River Laboratories
Description
Senior Research ScientistReq ID #: 222422
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
$ $118.00 US
per hour. 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, coordinates 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 ensures 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. Is an established key scientist in at least one area of expertise, with experience in different areas/disciplines.Responsibilities extended to include departmental, procedural or management of internal project(s) involvement and contributing to company growth (scientific and capabilities).
Job Description:
Job Qualifications
QUALIFICATIONS:
About Safety Assessment
Charles River is committed to helping our partners expedite their preclinical drug development with exceptional safety assessment services, state-of-the-art facilities and expert regulatory guidance.
From individual specialty toxicology and IND enabling studies to tailored packages and total laboratory support, our deeply experienced team can design and execute programs that anticipate challenges and avoid roadblocks for a smooth, efficient journey to market.
Each year approximately 300 investigational new drug (IND) programs are conducted in our Safety Assessment facilities.About Charles River
Charles River is an early-stage contract research organization (CRO).
We have built upon our foundation of laboratory animal medicine and science to develop a diverse portfolio of discovery and safety assessment services, both Good Laboratory Practice (GLP) and non-GLP, to support clients from target identification through preclinical development.
Charles River also provides a suite of products and services to support our clients' clinical laboratory testing needs and manufacturing activities.
Utilizing this broad portfolio of products and services enables our clients to create a more flexible drug development model, which reduces their costs, enhances their productivity and effectiveness to increase speed to market.
With over 20,000 employees within 110 facilities in over 20 countries around the globe, we are strategically positioned to coordinate worldwide resources and apply multidisciplinary perspectives in resolving our client's unique challenges.
At Charles River, we are passionate about our role in improving the quality of people's lives.
Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe.
We have proudly supported the development of 86% of the drugs approved by the FDA in 2021.Equal Employment Opportunity
Charles River Laboratories is an Equal Opportunity Employer - all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran or disability status.
If you are interested in applying to Charles River Laboratories and need special assistance or an accommodation due to a disability to complete any forms or to otherwise participate in the resume submission process, please contact a member of our Human Resources team by sending an e-mail message to [email protected] .
This contact is for accommodation requests for individuals with disabilities only and cannot be used to inquire about the status of applications.
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