Scientific Coordinator

Charles River LaboratoriesStilwell, KS, USonsiteSalary not postedView 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 Charles River Laboratories (CRL) is seeking a Scientific Coordinator to join our integrated toxicology (ITox) team at the Kansas City site. This site is the first of its kind, bridging CRL’s Discovery and Safety Assessment business units, while bringing automation to standard lead optimization toxicology study models to deliver rapid study results to our clients. When you join our team, you will have a significant impact on the health and well-being of people across the globe. The Scientific Coordinator role supports a key shift in the way studies are managed in SA, aligning with the vision of the integrated toxicology (ITox) business model. This role will be responsible for the coordination, supervision, and execution support of all study related activities at the facility while liaising closely with the study director. This role is also responsible for assisting in the compilation of study data/reports and providing study related information to Sponsors including written and verbal communication. The pay range for this position is $72,000 USD/annually. Job Description • Engage in the creation/customization of planning tools to facilitate prioritization of study deliverables • Interact regularly with sponsors: send amendments and documents for review and signature, respond to sponsor-requests for information and tables, and assist with sponsor on-site visits. • Serve as primary point of contact to the sponsor while working closely with the Study Director. • Preferred experience with lead optimization study design, execution and/or Discovery operations. • Serve as a model as it relates to effective time management, communication, and utilization of resources. Provide leadership and motivation to departmental personnel. • Ensure that schedule for study deliverables is met and any impacts to timelines are addressed promptly. • Monitor studies within the Vivarium and provide summarized details about animal health and study details as needed to study director, laboratory animal medicine, and/or Sponsor. • Excellent communication and interpersonal skills. • Strong leadership qualities including an agile mindset; understanding, collaborating, learning, and staying flexible to achieve high-performing results. • Demonstrated ability to multitask and problem solve in a fast-paced environment. • Familiar/comfortable at a higher volume/pace environment. • Write initial protocol drafts, distribute draft protocols for internal and/or sponsor review, and coordinate amendment/revision process. • Coordinate with principal investigator(s) internally and externally to ensure quality and timeliness of respective study phase. • Facilitate signature/approval process for protocols, amendments, and other required forms. • Generate, format, and review data for reporting. • Maintain study in-life and reporting timelines (deliverables). • Ensure that all study information is organized and quality controlled • Assist in IACUC form preparation and perform IACUC literature searches. • Assist in recording and remediation of study errors. • May conduct sponsor/visitor tours and interact with clients. • Through collaboration across functional areas at the site, be available to assist as experience allows to support overall study execution. • Perform all other related duties as assigned, including on study in-life procedures. Qualifications • Education : Bachelor’s degree (B.A./B.S.) or equivalent in scientific related discipline preferred. • Experience : 1-2 years experie

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