In-vivo Research Study Technician I

In-vivo Research Study Technician I Req ID #:  72752 Location: 

RTP, NC, US, 27709-2016 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. In-Vivo Research Technician I We are seeking an In-Vivo Research Technician Ifor our Insourcing Solutions site in Durham, NC.

The following are responsibilities related to the In-vivo Research Technician I: BASIC SUMMARY:

Execute survival and non-survival laboratory animal studies, including keeping appropriate records concerning those studies, and maintaining the equipment and facilities necessary for the successful progression of the research program. Place, maintain, and monitor animals under anesthesia while performing procedures. Broad range of technical skills involving various procedures with large and small animals.

ESSENTIAL DUTIES AND RESPONSIBILITIES:

• Communicate with sponsors to plan and execute proposed testing

• Assists with coordinating experiment efforts within the animal facility

• Uses imaging equipment (fluoroscope, ultrasound) to obtain images of test sites

• Trains other technicians and staff members on use of imaging equipment.

• Handle and restrain large animals (swine).

• Maintain animals under anesthesia and conduct procedures to include; catheter placement, drawing and analyzing blood samples, preparing intravenous solutions, minor surgical procedures, monitoring animals recovering from anethesia and necropsy.

• Responsible for execution of testing according to the established Standard Operating Procedures (SOPs) and protocols, and maintaining compliance with relevant quality system requirements, including GLP.

• Assist with writing and developing of new animal protocols and SOP’s.

• Document data collected to include study reports and publications.

• Engage in the development and execution of novel animal models and studies as well as the design and evaluation of new technologies for use in current and proposed studies.

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The following are the minimum qualifications related to the In-vivo Research Technician I: Education: Bachelor’s degree (B.S.) or equivalent in biology/life sciences or related discipline. Experience: 1 to 3 years related experience in a biological laboratory. An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.Swine animal handling experience preferred. Animal anesthesia (specifically inhaled anesthesia i.e. isoflourane and injectable). Clinical procedure experiences (venipuncture, catheter placement, blood draws, monitoring vitals, and administering medications) Certification/Licensure: LATG certification required.

About Insourcing Solutions

Charles River Insourcing Solutions℠ can streamline research by delivering operational and cost efficiencies through the strategic insourcing of GMP, GLP and non-GLP research services from discovery through safety assessment. Insourcing Solutions℠ provides you with the ability to maintain control of your facility and expertise while leveraging available space.

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 14,000 employees within 80 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. And in 2018, revenue increased by 22% to $2.27 billion from $1.86 billion in 2017.

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 ~85% of the drugs approved by the FDA in 2018.

Equal Employment Opportunity 

Charles River Laboratories is an Equal Opportunity Employer - M/F/Disabled/Vet

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