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Charles River Laboratories: Scheduler 1 Clinical Pathology 1

Charles River Laboratories

This is a Full-time position in Ashland, OH posted October 8, 2021.

At Charles River, we are passionate about improving the quality of people’s lives.

When you join our global family, you will help create healthier lives for millions of patients and their families.Charles River employees are innovative thinkers, who are dedicated to continuous learning and improvement.

We will empower you with the resources you need to grow and develop in your career.As a Charles River employee, you will be part of an industry-leading, customer-focused company at the forefront of drug development.

Your skills will play a key role in bringing life-saving therapies to market faster through simpler, quicker, and more digitalized processes.

Whether you are in lab operations, finance, IT, sales, or another area, when you work at Charles River, you will be the difference every day for patients across the globe.Job SummarySchedule all protocol-required tasks for in-life studies, ensuring proper placement of employees into specific study activities based on competency and responsibilities.

Additionally, schedule employee department and global trainings, and manage the department level study schedule and resources.Job QualificationsESSENTIAL DUTIES AND RESPONSIBILITIES:Support Study Supervisors, Research Associates and Team Leaders in the scheduling of all protocol-required tasks for in-life studiesLiaison with other departments in order to coordinate logistical challenges associated with the timing and collection of study-required tasksVerification and posting of all generated schedulesTroubleshoot logistical challenges associated with workload and study executionBe available to assist technicians with scheduling rearrangements in times of need (e.G., late doses, call-outs)Education: Associate’s degree (A.A./A.S.) or equivalent in scientific support/administrative or related discipline.Experience: 2 years of experience related experience in a laboratory or research environment.

Previous experience in a GLP environment preferred.An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.About Safety AssessmentCharles 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.