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Telemetry Support Scientist I
Charles River Laboratories International Inc (CRL)
Mattawan, MI, US, 49071
IMPORTANT: In order to be considered for this position, a resume/CV must be uploaded and submitted during the application process. Please make sure work history and education are added correctly.
Job Summary
We are seeking a Telemetry Support Scientist for our Study Directors- DSE group located in Mattawan, MI.
A Telemetry Support Scientist is responsible for: assisting with the design, development, and conduct of protocol specific and unique procedures, and pilot studies to evaluate physiology of animals; collecting, handling, and assisting with the interpretation of data from multiple species using basic to advanced techniques/instrumentation; assisting Telemetry Specialists, Study Directors, scientists, management, and other company personnel with study-related tasks; assisting with technology/process improvement initiatives; and training less-experienced personnel. A Telemetry Associate is responsible for: assisting with the design, development, and conduct of protocol specific and unique procedures, and pilot studies to evaluate physiology of animals; collecting, handling, and assisting with the interpretation of data from multiple species using basic to advanced techniques/instrumentation; assisting Telemetry Specialists, Study Directors, scientists, management, and other company personnel with study-related tasks; assisting with technology/process improvement initiatives; and training less-experienced personnel.
The pay range for this position is $24/hr. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.
Job Qualifications
The following are the minimum requirements related to a Telemetry Support Scientist position.
- HS/GED with 4 or more years of relevant experience; contract research organization experience preferred; and applicable certifications are a plus; or
- Bachelor’s/Master’s degree in a related field with at least 2 or more years of relevant experience; contract research organization experience preferred; and applicable certifications are a plus; or
- 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 short notice.
- Ability to work under specific time constraints.
Competencies
IMPORTANT: A resume is required to be considered for this position. If you have not uploaded your resume in your candidate profile, please return to upload field and attach your resume/CV.
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 20,000 employees within 110 facilities in 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 crrecruitment_US@crl.com. This contact is for accommodation requests for individuals with disabilities only and cannot be used to inquire about the status of applications.
Job posted: 2023-04-11
