Research Study Technician II

Research Study Technician II

19 Oct 2024
Massachusetts, Cambridge, 02138 Cambridge USA

Research Study Technician II

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 Summary We are seeking a Research Study Technician II for our Insourcing Solutions site in Cambridge, MA .The essential duties of the Research Study Technician II I are:

Reviews and complies with all policies, guidelines and operating procedures pertaining to the animal care and research program.

Provides technical procedure training to less experienced staff and researchers, and provide re-training as needed.

May coordinate (or assist) or manage schedules of other team members; resolves schedule conflicts Assemble, set up, operate and maintain any necessary experimental equipment to conduct in-vivo studies.

Conduct laboratory procedures in compliance with established protocols/plans and with regulatory and laboratory requirements

Able to perform the following techniques in rodent

PO, IV, SQ, IP, IM, and IN dosing and/or inoculation techniques

Blood collection from multiple vessels or cardiac, and perfusions

Tumor measurements, body weights, IBD and EAE scoring, behavioral monitoring, etc.

Job Qualifications The following are minimum requirements related to the Research Study Technician II position:

B.S./B.A. degree in Biological Sciences or related field, or associate's degree in veterinary technology or equivalent college level program.

Must have at least 4 years of previous laboratory animal research experience. At least 3 years of technical experience as detailed in the essential duties and responsibilities section.

The pay range for this position is $30.00 - $35.00 per hour. Please note that salaries vary within the range based on factors including experience, skills, education, certifications, and location.About Insourcing SolutionsCharles 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 RiverCharles 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 20,000 employees within 110 facilities in over 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.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 worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.We're committed to providing benefits that elevate your quality of life. Based on your position these may include: bonus/incentives based on performance, 401K, paid time off, stock purchase program, Health and wellness coverage, employee and family wellbeing support programs, and work life balance flexibility.Equal Employment OpportunityCharles River Laboratories is an Equal Opportunity Employer - all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, or national origin, veteran or disability status.If you are interested in applying to Charles River Laboratories and need special assistance or an accommodation due to a disability to complete any forms or to otherwise participate in the resume submission process, please contact a member of our Human Resources team by sending an e-mail message to crrecruitmentUS@crl.com. This contact is for accommodation requests for individuals with disabilities only and cannot be used to inquire about the status of applications.For more information, please visit www.criver.com.224983

Related jobs

  • 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.

  • The Senior Manager Clinical Study Lead (CSL) is expected to operate with high-degree of independence and is accountable for the global execution of assigned large and/or complex clinical trials from study design, through execution, to study close out. The Senior CSL is accountable for the study timelines, study budget, and ensuring study conduct is in accordance with Regeneron Standard Operating Procedures (SOPs) and ICH/GCP. This role applies to internally sourced studies and studies out-sourced to Clinical Research Organizations (CROs) and the balance of direct leadership versus oversight will vary accordingly. Contributes and drives ongoing process improvement initiatives.

  • Video Monitoring Technician - ( 3311756 )

  • The Senior Clinical Study Lead (CSL) is expected to operate with high-degree of independence and is accountable for the global execution of assigned large and/or complex clinical trials from study design, through execution, to study close out. The Senior CSL is accountable for the study timelines, study budget, and ensuring study conduct is in accordance with Regeneron Standard Operating Procedures (SOPs) and ICH/GCP. This role applies to internally sourced studies and studies out-sourced to Clinical Research Organizations (CROs) and the balance of direct leadership versus oversight will vary accordingly. Contributes and drives ongoing process improvement initiatives.

  • About the Job

  • Microsoft Research New England is looking for a postdoctoral researcher interested in bringing sociotechnical perspectives to analyze critical issues of our time. They will join a team of social scientists who use empirical and critical methods to study the social, political, and cultural dynamics that shape technologies and their consequences. Our work draws on and spans several disciplines, including anthropology, communication, gender and sexuality studies, history, information studies, law, media studies, organizational and management sciences, science & technology studies, and sociology.

  • About the Job

Job Details

Jocancy Online Job Portal by jobSearchi.