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Report Adminstrator I, Report Writing 1

Report Adminstrator I, Report Writing 1
Req ID #: 37618
Location:
Ashland, OH, US, 44805
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.
We are seeking an experienced Report Administrator I for our Safey Assessment site located in Ashland, Ohio.
Responsible for production of data tables from various data collection systems, basic publishing tasks (assemble and publish full reports), and finalization of phase and full study reports for assigned studies in accordance with Good Laboratory Practice Regulations and Standard Operating Procedures with a moderate level of supervision/instruction. Responsibilities include review of study records and preparation of methodology section of reports, preparation of all report tables and figures, and finalization of study reports for submission to the client and governmental regulatory agencies.
ESSENTIAL DUTIES AND RESPONSIBILITIES:
Assist study director and department management in monitoring progress of assigned studies
Familiarity with Standard Operating Procedures
Compilation of study information not recorded online
Collation and quality control of data
Preparation, verification, and proofreading of report tables
Routine print-editing of WTDMS? report tables and post-processing of Provantis report tables
Running statistical analysis programs
Generation of manual report tables, Common Technical Documents (CTD), and any other regulatory agency summary table requirement(as needed)
Maintaining active record of data table and report transfers during generation and review
Assist with QA audits
Generation and publication of electronic reports using appropriate publishing software
Collaboration with study director, departmental personnel, and client (as necessary) for review and incorporation of client comments
Collaboration with other appropriate company personnel as needed
Regular and punctual attendance
Comply with all Charles River policies and procedures
Follow all safety rules and regulations
Adhere to all environmental regulations
Attend and participate in all required training sessions
Work as a team member
Ability to understand and follow oral and written instructions
Other duties as assigned by departmental management
QUALIFICATIONS:
Education: AS degree in a natural sciences/technical writing/computer sciences field
Experience:
Certification/Licensure: None
Other: Completed training in use of Provantis, Nevis, WTDMSTM (including print-editing), Word, and appropriate publishing software. Key skills include attention to detail, personal
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 11,000 employees within 70 facilities in 18 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. And in 2016, revenue increased by 23.3% to $1.68 billion from $1.36 billion in 2015.
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 70% of the drugs approved by the FDA in 2016.
For more information, please visit www.criver.com.
Charles River Laboratories, Inc. is an Equal Opportunity Employer M/F/Disabled/Vet
Nearest Major Market: Cleveland
Nearest Secondary Market: Mansfield
Job Segment: Toxicology, Biotech, Pharmaceutical, Laboratory, Science, Research



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