IACUC coordinator

IACUC coordinator Req ID #:  98978 Location: 

Reno, NV, US, 89511

For 70 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 Summary

We are seeking a IACUC Coordinatorfor our Safety Assessment site located in Reno, Nevada.

The IACUC Coordinatoris responsible for coordinating IACUC functions and the IACUC review process. Generates reports for semi-annual facility inspections and program reviews and maintains the IACUC databases. Performs recordkeeping, reporting to regulatory agencies and maintaining documentation for regulatory accreditation and licensure. Performs administrative functions for the Laboratory Animal Medicine department.

ESSENTIAL DUTIES AND RESPONSIBILITIES:

• Pre-screen IACUC submissions for completeness and assign reviewers.

• Maintain electronic and hard copies of all protocols, amendments and IACUC approvals for Charles River Laboratories, Safety Assessment, Nevada.

• Update and maintain records for all matters concerning the IACUC and LAM including applicable databases.

• Generate agendas and minutes for monthly IACUC meetings.

• Generate and revise IACUC policies.

• Generate semi-annual inspection and program review reports. Assist the IACUC Committee with conducting facility inspections.

• Act as a liaison between study directors, study coordinators and the IACUC Committee.

• Generate reports, maintain, and monitor licensure and accreditation required by the USDA, OLAW, AAALAC, U.S. Fish and Wildlife, CDC, and State of Nevada Radiology.

• Perform administrative and clerical support functions as assigned.

• Assist in the development, maintenance, and communication of departmental systems and SOPs.

• Coordinate conventions, seminars, travel and candidate interviews for management staff.

• Prepare and assist senior management with contractual and confidentiality agreements.

• Perform other related duties as required.

MINIMUM QUALIFICATIONS:

• Education: Associate’s degree (A.A./A.S.) or equivalent preferred.

• Experience: 3-5 years administrative experience. Experience working in a laboratory animal environment preferred.

• 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: Knowledge of USDA regulations, AWA, PHS policy, AAALAC regulations, and “the Guide” preferred. Excellent organizational skills, especially with time management and record keeping. Strong computer skills (Microsoft Office Suite). Must be able to work independently. Excellent written and verbal communication skills.

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.

Nearest Major Market: Reno

Nearest Secondary Market: Tahoe

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