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Study Supervisor 1
Charles River Laboratories International Inc (CRL)
Reno, NV, US, 89511
Job Summary
The pay range for this position is $79,000.00 -$80,000.00 USD per hour. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.
We are seeking an experienced Study Supervisor (Tech Ops) for our Safety Assessment site located in Reno, Nevada.
The Study Supervisor will be responsible for managing the technical staff in assigned area. Responsible for preparing, conducting/orchestrating, and overseeing technical activities in studies of short duration and small size. Ensure compliance with all applicable regulations and with departmental policies, practices and procedures (e.g., SOPs, protocols). Also responsible for front-line oversight and coordination of all study-related activities.
The following are minimum requirements related to the Study Supervisor position.
- Bachelor’s degree (B.A./B.S.) or equivalent in science or related discipline.
- 2-3 years related experience in a GLP environment and experience with research and investigative procedures, techniques, and literature.
- An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.
- AALAS certification or other applicable professional certification preferred.
- Ability to handle multiple projects, prioritize work and meet deadlines. Effective written and verbal communication skills. Knowledge of GLPs and other federal regulations and guidelines relating to the care of laboratory animals required. Advanced technical and analytical skills; problem solving and leadership skills. Computer literate.
Job Qualifications
Qualificatons related to the Study Supervisor position.
- Bachelor’s degree (B.A./B.S.) or equivalent in science or related discipline.
- 2-3 years related experience in a GLP environment and experience with research and investigative procedures, techniques, and literature.
- An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.
- AALAS certification or other applicable professional certification preferred.
- Ability to handle multiple projects, prioritize work and meet deadlines. Effective written and verbal communication skills. Knowledge of GLPs and other federal regulations and guidelines relating to the care of laboratory animals required. Advanced technical and analytical skills; problem solving and leadership skills. Computer literate.
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. Our client base includes global pharmaceutical companies, biotechnology companies, government agencies and hospitals and academic institutions around the world.
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.
Job posted: 2024-04-17
