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Charles River Laboratories: Research Associate 3 1

Charles River Laboratories

This is a Full-time position in Ashland, OH posted October 7, 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 SummaryCoordinates study related activities of research technical staff to ensure compliance with the protocol and applicable SOP’s and maintains the raw data for nonclinical studies.

Provide guidance and mentoring to less experienced staff.Job QualificationsESSENTIAL DUTIES AND RESPONSIBILITIES:Ability to perform all functions required of Research Associate I and II.Provides training plans and training for junior level Research Associates.Maintains resource guides for data collation and study set-up with assistance from Research Associate II.Reviews work schedules or other data collection protocols.Coordinates and oversees Research Associate shadowing program.Works with Technical Operations management to contribute to research policies and procedures.Begins to communicate with Sponsor representatives on protocol-driven, study-related activities conducted by Technical Operations.Assist Study Director with client visits.Able to assistant in interview process for new Study Directors.Participate in team meetings.Perform all other related duties as assigned.QUALIFICATIONS:Education: Bachelor’s degree (B.A./B.S.) or equivalent in related scientific discipline.Experience: 6-8 years of related experience in a GLP environment.

At least 2 years of experience in the Research Associate II role.An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.Certification/Licensure: LAT preferredOther: Ability to organize, prioritize work and meet deadlines.

Computer literacy with word processing, spreadsheet and data base programs.

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.