Coordinator In Vivo Services

Coordinator In Vivo Services Req ID #:  204712 Location: 

Shrewsbury, MA, US, 01545 For 75 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 we perform. In return, we’ll help you build a career that you can feel passionate about.

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 Charles River Laboratories is seeking a Coordinator within our InVivo Services Team at our Safety Assessment site located in Shrewsbury, MA.   The coordinator will be involved in all aspects of facility and study scheduling within the InVivo group.   This individual will work closely with management, study directors, and vendors.    

Responsibilities include but not limited to: All aspects of study scheduling including initiation, collections, data review and shipments Assist with facility inspections and audits including USDA and client based Animal ordering Order and maintain an inventory of laboratory supplies and equipment Preparation of reagents Communicate delivery and return of samples and reference standards to sponsors Ensure that raw data records are accurate, complete, and in appropriate order Job Qualifications Education:   Associate degree (A.A./A.S.) or equivalent in a science or related discipline.  Bachelor’s degree preferred Experience:  Minimum 2-4 years related laboratory experience, preferably in a pharmaceutical or contract laboratory environment. An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education listed above. Certification/Licensure:   None Other: Ability to effectively communicate orally and in writing.  Understanding of regulatory requirements of study types assigned, as well as Testing Facility SOPS and GLPs, as appropriate.   Ability to organize and prioritize work to meet deadlines under minimal direction.  Proficiency in standard software.  Ability to use basic lab equipment such as pH meter, sonicator, and homogenizer.   Basic understanding of study design and protocols.

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.

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

Nearest Major Market: Worcester

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