Report Assistant
Spencerville, OH, US, 45887
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 Report Assistant for our Report Coordination Team at our Safety Assessment site located in Spencerville, OH.
Assist with publishing scientific data tables and establishing the framework of reports. Develop the Introduction and Methods sections of Draft Reports for Charles River Laboratories, Safety Assessment studies. Perform electronic report compilation of assigned studies.
Essential Functions (The fundamental Competencies/Skills & Responsibilities of the role (products and services provided/results accomplished) include, but are not limited to, those listed:
- Assist in generating scientific data tables and establish the framework for reports.
- Draft the Introduction and Methods sections of study reports, with guidance. Participate in the creation of Materials and Methods and Summary sections of reports, with guidance.
- Perform electronic report compilation of assigned studies.
- Ensure that all protocol and amendment requirements are met with respect to final report data.
- Keep current with changing technology.
- Input electronically transferred data from available resources as necessary.
- Compile documents into draft and final integrated reports.
- Participate in pre-study meetings as assigned.
- Perform all other related duties as assigned.
The pay range for this position is $20-23/hr. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.
Job Qualifications
(Knowledge, Experience, Skills and Abilities required to accomplish the essential functions) include but are not limited to:
- Education: Associate’s degree (A.A./A.S.) in journalism, computer science, business administration or related discipline preferred. Bachelor’s degree (B.A./B.S). in biological sciences, computer science, business administration, or related discipline desired.
- Experience: 0 to 1 year related experience in a GLP environment and/or scientific data presentation, writing, editing, proofreading and publishing.
- An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.
- Certification/Licensure: None.
- Other: Proficient with spreadsheet, database, and publishing software (e.g. MS Excel®, Word®, and Adobe® Acrobat® PDF software). Strong written, verbal, and analytical skills. Familiar with medical terminology. Familiar with preclinical study protocols/reports preferred. Familiarity with Provantis™ system and/or Nevis preferred.
Physical Demands:
- Must regularly operate a computer and occasionally operate other office productivity machinery such as a calculator, copy machine, and computer printer.
- Must regularly communicate with employees/customers; must be able to exchange accurate information.
- Must occasionally move about inside the office to access file cabinets, office machinery, etc.
Work Environment:
- General office working conditions, the noise level in the work environment is usually quiet.
Comments:
- This position may require overtime, weekend, and/or after hours shift coverage, as needed.
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 300 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 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 (including sexual orientation, gender identity, and expression), 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 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.
For more information, please visit www.criver.com.
Nearest Major Market: Lima
Nearest Secondary Market: Findlay
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