Clinical Support Services Coordinator I

Charles River LaboratoriesShrewsbury, MA, USonsite$24–$27/hrView the original posting at Charles River Laboratories ↗

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. Job Overview We are seeking a Clinical Support Coordinator I to join our Clinical Support Services Team for our Safety Assessment site located in Shrewsbury, MA . The ideal candidate is detail oriented, has excellent communication skills and has a general familiarity with lab procedures. Job Description A Clinical Support Coordinator I provides project support to ensure the timely delivery of clinical materials and shipments. Additionally, this person is responsible for maintaining documentation and records relating to clinical kitting and communicating actively and clearly with multiple parties about clinical supply shipments and deliverables. P reparing, reviewing, and shipping clinical study kits and supplies according to SOPs and study requirements. Actively and clearly communicating with clinical sites, clients, and internal teams regarding study activities related to clinical kitting. Assisting with the development and customization of study materials, site manuals, and clinical kits. Creating and maintaining studies within a Laboratory Information Management System (LIMS). Reviewing study protocols and client documentation to identify study setup and reporting requirements. Coordinating the flow of study information between clients, clinical kitting and analysis teams. Ensuring compliance with company SOPs, quality standards, and regulatory guidelines. Maintaining accurate, complete, and organized data and study documentation. Providing support to other departments and service lines as needed. Performing additional duties assigned by management. Job Qualifications Education: Bachelor’s degree preferred. Experience: 1-year related experience in a life science laboratory. An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above. Certification/Licensure: None. Other: Must be detail-oriented and have general familiarity with lab procedures. Good verbal communication skills required. Ability to organize and prioritize work to meet deadlines under minimal direction. Basic computer skills; familiarity with Microsoft Office software. The pay range for this position is between $24-27/hr. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location. 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 300 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

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