IMPORTANT: In order to be considered for this position, a resume/RESUME 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 Telemetry Team located in Mattawan, MI.
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. 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.
Job Qualifications
The following are the minimum requirements related to a Telemetry Associate 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
Lead – We lead when we advocate our purpose and model our values, when we deliver innovation, when we embrace change, and when we appreciate and celebrate the great work of others.
Care – We show we care when we respect each other, our animals and the communities where we work and live, when we create a positive healthy workplace, when we are mindful of our compliance standards, and when we choose to do the right thing.
Collaborate -We collaborate when we partner with each other and promote teamwork, when we communicate clearly and effectively across the hall or around the globe, and when we welcome all forms of diversity and encourage inclusiveness.
Own – We act like owners when we hold ourselves accountable for our actions, when we respond to internal and external client needs with speed and accuracy, when we set and achieve meaningful goals, and when we strive towards continuous improvement.
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/RESUME.
Vaccine Mandate
Charles River is a U.S. Federal Contractor. As a result, we must follow the Presidential Executive Order to mandate vaccinations, and ensure our employees are fully vaccinated against COVID-19 by December 8, 2021. Our main priority is the wellbeing, health, and safety of our people. We will be requiring proof of vaccination from all employees.
Anyone with requests for disability-related and/or religious exemptions should contact Talent Acquisition ((url removed)) so that information can be provided about the accommodation process at Charles River.
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.
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