Clinical Materials & Sample Logistics Coordinator

RXinsider LTD.; Shrewsbury (MA); On-site; USD 33,000 - 37,000; Full time

Job summary

Charles River Laboratories in Shrewsbury, MA is seeking a Clinical Support Coordinator I to join the Safety Assessments team. The role focuses on supporting the timely delivery of clinical materials and the handling of biological samples in a GLP/SOP framework.

The successful candidate will assist in kit design, inventory management, and cross-functional coordination with bioanalytical teams, ensuring accuracy and adherence to protocols across study workflows.

Qualifications

• Detail oriented candidate with strong accuracy and organizational skills.
• Excellent communication abilities to interact with clients, partners and internal teams.
• General familiarity with lab procedures and GLP/SOP context as relevant to clinical materials handling.

Responsibilities

• Provide project support to ensure timely delivery of clinical materials and shipments.
• Receive, ship and manage inventory of biological samples per SOPs and GLPs.
• Create, review and ship clinical kits and supplies under guidance of senior personnel.
• Assist in customization and design of site manuals, clinical kits and materials.
• Coordinate flow of study information between clients and bioanalytical teams.
• Read study protocols and extract reporting requirements for study creation.
• Follow company SOPs to ensure data integrity and regulatory compliance.
• Provide cross-functional support to other service lines as needed.

Skills

Detail oriented

Excellent communication

Lab procedures familiarity

Job description

Charles River Laboratories in Shrewsbury, MA is seeking a Clinical Support Coordinator I to join the Safety Assessments team. The role focuses on supporting the timely delivery of clinical materials and the handling of biological samples in a GLP/SOP framework.

The successful candidate will assist in kit design, inventory management, and cross-functional coordination with bioanalytical teams, ensuring accuracy and adherence to protocols across study workflows.