Analytics Associate (Mattawan, MI, US, 49071)

<p><span style="font-size:10.0px"><span style="font-family:Arial, Helvetica, sans-serif">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.</span></span></p> <div><div style="padding:10.0px 0.0px;border:1.0px solid transparent"><div style="font-size:16.0px;word-wrap:break-word"><H2 style="font-size:1.0em;margin:0.0px"><b>Job Overview</b></H2> </div><div><p>An Analytics Associate is responsible for producing custom tables with statistical analyses using established systems and / or standardized code, to be completed in an accurate and timely manner consistent with the direction provided by the study director.</p></div></div><div style="padding:10.0px 0.0px;border:1.0px solid transparent"><div style="font-size:16.0px;word-wrap:break-word"><H2 style="font-size:1.0em;margin:0.0px"><b>Job Description</b></H2> </div><div><ul> <li>Produce data listings, summaries, graphs, and statistical analysis results for report writing using established systems and/or standardized code. Minor, study-specific changes may be made to standardized code files as required by the study design and will be reviewed during the output verification process.</li> <li>Review data to verify integrity and consistency for completeness, accuracy, and suitability, including data adherence to protocol, data coding integrity, reliability of collection, and interpretation.</li> <li>Maintain organized, complete, and up-to-date study documentation, testing, and validation/quality control documents and programs in compliance with company standards and GLP guidelines.</li> </ul> <p> </p> <p><strong>Minimum Qualifications:</strong></p> <ul> <li>Education and Experience: Bachelor’s degree (mathematics, statistics, or computer science preferred); contract research organization experience preferred.</li> <li>Ability to communicate verbally and in writing at all levels inside and outside the organization.</li> <li>Basic familiarity with Microsoft Office Suite.</li> <li>Experience with Excel is required.</li> <li>Computer skills, commensurate with Essential Functions, including the ability to learn a validated system.</li> <li>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.</li> <li>Ability to work under specific time constraints.</li> <li>Must be authorized to work in the United States without a sponsor visa, now or in the future.</li> </ul> <p><br><strong>The pay for this role is $27/hour.</strong></p></div></div><div style="padding:10.0px 0.0px;border:1.0px solid transparent"><div style="font-size:16.0px;word-wrap:break-word"><H2 style="font-size:1.0em;margin:0.0px"><b>Education</b></H2> </div><div><div>No degree required</div></div></div><div style="padding:10.0px 0.0px;border:1.0px solid transparent"><div style="font-size:16.0px;word-wrap:break-word"><H2 style="font-size:1.0em;margin:0.0px"><b>Physical Requirements</b></H2> </div><div></div></div></div><p><span style="font-size:10.0px"><span style="font-family:Arial, Helvetica, sans-serif"><b>About Safety Assessment</b><br> 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 300 investigational new drug (IND) programs are conducted in our Safety Assessment facilities.</span></span></p> <p><br> <span style="font-size:10.0px"><span style="font-family:Arial, Helvetica, sans-serif"><b>About Charles River</b><br> 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.</span></span></p> <p><span style="font-size:10.0px"><span style="font-family:Arial, Helvetica, sans-serif">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.</span></span></p> <p><span style="font-size:10.0px"><span style="font-family:Arial, Helvetica, sans-serif">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.</span></span></p> <p><span style="font-family:Arial, Helvetica, sans-serif"><span style="font-size:10.0px"><span><span style="color:#333333">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.</span></span></span></span></p> <p> </p> <p><span style="font-size:10.0px"><span style="font-family:Arial, Helvetica, sans-serif"><b>Equal Employment Opportunity</b></span></span></p> <p><span style="font-size:10.0px"><span style="font-family:Arial, Helvetica, sans-serif">Charles River is an equal opportunity employer and is committed to providing equal employment opportunities for all qualified applicants and employees without regard to race, color, sex, religion, national origin, ancestry, age, mental or physical disability, family status, pregnancy, military or veteran status, or any other characteristic protected by federal, state, or local laws.</span></span></p> <p><span style="font-size:10.0px"><span style="font-family:Arial, Helvetica, sans-serif">It is unlawful in some states (including Massachusetts) to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.</span></span></p> <p><span style="font-size:10.0px"><span style="font-family:Arial, Helvetica, sans-serif">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 crrecruitment_US@crl.com. This contact is for accommodation requests for individuals with disabilities only and cannot be used to inquire about the status of applications.</span></span></p> <p> </p> <p><span style="font-size:10.0px"><span style="font-family:Arial, Helvetica, sans-serif">For more information, please visit www.criver.com.</span></span></p>