Sorry, this job is no longer available.

Report Coordinator Associate - Report Services

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 an Report Coordinator Associate for our Report Services Team located in Mattawan, MI. 



The Report Coordinator Associate is responsible for: coordinating the reporting processes to produce quality, on-time reports; providing support for assigned Study Director(s); and prioritizing his/her
workload. Good communication skills and the ability to adhere to deadlines are necessary for success.



The following are the minimum requirements related to the Report Coordinator Associate position.



  •  HS/GED with 4 or more years of relevant experience; contract research organization experience preferred, or
  •  Bachelor’s/Master’s degree in a relevant field with 0-2 or more years of relevant experience; contract research organization experience preferred.
  •  Demonstrated ability to prioritize daily tasks.
  •  Demonstrated ability to use critical thinking to anticipate and resolve study-related issues.
  •  Demonstrated knowledge of the reporting process.
  •  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 constraint.



About MPI Research, a Charles River Company

MPI Research is a premier non-clinical contract research organization (CRO) providing comprehensive testing services to biopharmaceutical and medical device companies worldwide.


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 13,000 employees within 80 facilities in 23 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 80% of the drugs approved by the FDA in 2017.


For more information, please visit


Equal Employment Opportunity
Charles River Laboratories, Inc. is an Equal Opportunity Employer M/F/Disabled/Vet