Study Supervisor:
Charles River Laboratories

30221-en_US
Charles River Laboratories
Reno Nevada
Biotech
Description

For nearly 70 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 e perform. In return, we’ll help you build a career that you can feel passionate about.


Responsibilities

We are seeking an experienced Study Supervisor for our Safety Assessment site located in Reno, Nevada

In addition to managing the technical staff in the assigned area, the Study Supervisor will be 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.

  • Bachelors 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.
  • Must be able 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.  Must be computer literate.

 

About Safety Assessment Business

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 120 investigational new drug (IND) programs are conducted in our Safety Assessment facilities.

Salary Grade: 83


Who May Apply

The policy of Charles River Laboratories is to provide advancement opportunities to all qualified employees within the company through transfers or promotions.
Regular Full and Part Time employees may apply for a Job Posting if they meet the eligibility requirements set forth in the Internal Job Posting policy.
Regular Full and Part Time Employees must complete at least one year of continuous active service in their position prior to applying.
Regular Full and Part Time Employees are eligible to participate in the Job Posting Process if their current overall performance appraisal rating is equivalent to "satisfactory" or better.
Regular Full and Part Time Employees cannot be in any stage of a disciplinary action.
Regular Full and Part Time Employees on leave of absence are not eligible to apply.

 

 

 

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 120 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 11,000 employees within 70 facilities in 18 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. And in 2016, revenue increased by 23.3% to $1.68 billion from $1.36 billion in 2015. 

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 ~70% of the drugs approved by the FDA in 2016.

For more information, please visit www.criver.com.

 

Equal Employment Opportunity

 

Charles River Laboratories, Inc. is an Equal Opportunity Employer M/F/Disabled/Vet

Basic Qualifications
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