Communications Manager

Communications Manager Charles River Laboratories - 3.1 Memphis, TN Job Details Full-time $115,000 a year 17 hours ago Benefits Health insurance Paid time off Qualifications Presentation software Marketing Word processing Writing skills Content writing Marketing Full Job Description Req ID #: 233849 Memphis, TN, US Full time 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 Overview Charles River Corporate Communications team is seeking a Full Time Internal Communications Manager to support our Global Biologics Solutions (CDMO). The Internal Communications Manager will develop content and implement internal communication strategies and plans that engage, align and inspire employees with Charles River's vision and business strategy and drive employees' understanding of and engagement with Charles River's priorities and key initiatives. Develop and publish content using electronic tools, including Sharepoint, Poppulo, and Digital Signage. Support global communications for the Global Biologics Solutions - CDMO Business.

Job Description Essential Duties and Responsibilities:

Work closely with Sr. Manager, Employee Communications on communication strategies and activities to support the global Biologics Solutions - CDMO business (sites located in Keele, Rockville, Memphis) Assist with development of messaging and internal communications for company updates, key initiatives, and other topics. Assist with implementation of onsite communications strategies, programs or activities that address specific business issues or employee needs and achieve desired results including newsletters (digital and print), digital signage, and SharePoint/intranet. Maintain site and business segment presence on Yammer and SharePoint. Assist local site communications leads with Employee Engagement efforts, including planning and executing onsite events and activities. Assist with video production for internal purposes. Create clear, concise and timely communications that convey key messages tied to business/company goals and foster employee understanding and commitment. Develop well-crafted written material for a variety of audiences and for various communication vehicles including the intranet, e-mail, digital signage, newsletters, and print collateral. Assist with measurement of communications effectiveness using best practices and KPIs. Perform all other related duties as assigned.

Qualifications:

Education:

Bachelor's degree (B.A./B.S.) or equivalent in communications, public relations, marketing or related discipline.

Experience:

1-3 years related experience in corporate communications with a focus on internal audiences and content and digital channel development. An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.

Other:

Excellent writing, marketing and communications skills required. Proficiency in creating word-processed documents, spreadsheets, and presentations required. Basic video production and design skills preferred. SharePoint, PowerPoint, and other digital platform skills preferred. Compensation Data The pay rate for this role is $115,000 per year. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location. Physical Requirements About Charles River's CDMO Services With over 20 years of experience and industry-leading expertise, Charles River's cell and gene therapy Contract Development and Manufacturing Organization (CDMO) group supports biotechnology and pharmaceutical companies in advancing their complex programs from early development through commercialization. Our integrated, phase-appropriate CDMO capabilities—including plasmid DNA, viral vector, and cell therapy manufacturing—enable seamless development and faster timelines. With centers of excellence in the US and UK, we offer GMP-compliant and research-grade solutions, along with comprehensive analytical services and regulatory support. Whether clients need end-to-end development, standalone services, or insourced support, our CDMO team provides custom solutions to meet evolving program needs. From process development in Hanover to viral vector manufacturing in Rockville, large-scale cell therapy production in Memphis, and plasmid DNA services in Keele, we simplify the supply chain and accelerate cell and gene therapy breakthroughs. 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 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 Opportunity 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. 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. 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 . 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.