Research Analyst I - Pharmacy
Charles River Laboratories International Inc (CRL)
Mattawan, MI, US, 49071
Research Analyst I - Pharmacy Req ID #: 200320 Location:
Mattawan, MI, US, 49071 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 Analyst I for our Test Material Control/Pharmacy Department site located Mattawan, MI.
A Research Analyst I - Test Material Control (TMC)/Pharmacy is responsible for: preparing, sampling, and dispensing formulated test material according to applicable Standard Operating Procedures (SOPs) and GxP guidelines. The individual in this role: completes projects on time while maintaining quality and efficiency; communicates effectively with management, internal customers, and team members; assists others with their duties; and may assist with troubleshooting formulation issues.
Standard working hours will be Monday - Friday, 07:00am-3:30pm. Depending on assigned shift, additional hours could be required or requested during nights, weekdays, weekends and/or holidays.
Qualifications The following are minimum Qualifications related to the Research Analyst I position:
HS/GED with 0-6 months of relevant experience; contract research organization experience preferred. Bachelor’s/Master’s degree in a relevant field with no experience; contract research organization experience preferred. Ability to communicate verbally and in writing at all levels inside and outside the organization. Basic familiarity with Microsoft Office Suite. Computer skills, commensurate with Essential Functions, including the ability to learn a validated system. Ability to work extended hours beyond normal work schedule to include, but not limited to evenings, weekends, extended shifts, and/or extra shifts; sometimes on short notice. Ability to work under specific time constraints.
Competencies Collaborate -We collaborate when we partner with each other and promote teamwork, when we communicate clearly and effectively across the hall or around the globe, and when we welcome all forms of diversity and encourage inclusiveness.Own - We act like owners when we hold ourselves accountable for our actions, when we respond to internal and external client needs with speed and accuracy, when we set and achieve meaningful goals, and when we strive towards continuous improvement.Care - We show we care when we respect each other, our animals and the communities where we work and live, when we create a positive healthy workplace, when we are mindful of our compliance standards, and when we choose to do the right thing.Lead - We lead when we advocate our purpose and model our values, when we deliver innovation, when we embrace change, and when we appreciate and celebrate the great work of others.
Charles River is a U.S. Federal Contractor. As a result, we must follow the Presidential Executive Order to mandate vaccinations, and ensure our employees are fully vaccinated against COVID-19. Our main priority is the wellbeing, health, and safety of our people. We require proof of vaccination from all employees.
Anyone with requests for disability-related and/or religious exemptions should contact Talent Acquisition ([email protected]) so that information can be provided about the accommodation process at Charles River.
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.
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 supported the development of 86% of the drugs approved by the FDA in 2021.
Equal Employment Opportunity
Charles 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, 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 [email protected] 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.
Nearest Major Market: Kalamazoo
Job Segment: Pharmaceutical, Recruiting, Laboratory, Biotech, Research, Science, Human Resources
Similar CRA jobs
Senior Clinical Research Associate, CNS, Central - IQVIA Biotech
Analyst - Primary Market Research
Clinical Data Analyst
Research Scientist/Senior Research Scientist - Surgery and Efficacy Study Directors
Observational Research Specialist II - German Speaker
Analyst Immunology (Sherbrooke)
Initiation Clinical Research Associate II/Senior iCRA (study start-up)
Clinical System Set-up Analyst (multiple European locations)
Research Technician 2 (Surgery)
Research Scientist Team Lead- Oncology
Commercial Effectiveness Analyst, UK
Sr. Clinical Contract Analyst - FSP
Research Assistant 1 (Molecular Biology) 1
Research Associate (Japanese Speaking)
IT Analyst I
Senior Clinical Research Associate, Oncology (France) - Iqvia Biotech
Research Technician - Second Shift | General Toxicology *$1000 sign-on bonus 1
Financial Analyst II - Project Finance
Pharmacy Tech - Sterile Products