Data Review Associate - Necropsy

Charles River Laboratories International Inc (CRL)

Horsham, PA, US, 19044

Data Review Associate - Necropsy Req ID #:  204551 Location: 

Horsham, PA, US, 19044 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.


IMPORTANT:   In order to be considered for this position, a resume/CV must be uploaded and submitted during the application process.  Please make sure work history and education are added correctly.   

  Job Summary Full Time - Partially Remote


Responsible reviewing advanced study data to ensure it is complete, accurate and collected in line with GLP requirements.  Ensure that all data received for review follows SOP guidelines that apply to the recording of study data.  Act as a liaison for departmental projects, interact with other departments as needed to support data review and delivery, and support training activities as they relate to data.


⦁    Complete data review for advanced study data. Review would include all paper and electronic data produced in operational departments.  

⦁    Ensure all data corrections are completed by the appropriate staff members.

⦁    Work with peers and management team to implement or refine processes and procedures for data review, including revising or developing departmental forms and updating SOPs as appropriate.

⦁    Communicate with department management and supervisors regarding issues related to data collection that impact the integrity of the data.

⦁    Escalate critical data issues immediately to management.

⦁    Collaborate with Quality Assurance to refine understanding of GLP data review expectations and embed these tenets in the training program.

⦁    Ensure that data are collated and organized in line with departmental expectations prior to deliver to Study Director.

⦁    Accurately capture corrective actions required in designated tools and support identification of trends to enable focus on data review training for the group.

⦁    Actively participate in data quality and deviation reduction initiatives within and between departments.

⦁    Support timely, accurate completion of audits and follow-up items.

⦁    Assist in mentoring/training staff on data review procedures and developing and updating departmental data training standards. 

⦁    Perform other related duties as required.

  Job Qualifications QUALIFICATIONS:

⦁    Education:  Bachelors degree or above preferred.

⦁    Experience:  Minimum of 1-2 years previous laboratory experience required, preferably in a pharmaceutical or contract laboratory environment.

⦁    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


⦁    While performing the duties of this job, the employee is regularly required to talk and hear.    

⦁    Specific vision abilities required by this job include regular use of close vision and the ability to adjust focus.

⦁    Must be able to regularly sit approximately six hours a day.

⦁    Must be able to regularly read and transcribe typewritten or handwritten information into a personal computer and make edits on information therein.

⦁    Regularly required to type for three to four hours at a time.

⦁    Regularly operates all office equipment.  


⦁    General office working conditions.  The noise level in the work environment is usually quiet.

⦁    Occasionally works near toxic or caustic chemicals and test articles with unknown levels of toxicity. 

⦁    May occasionally be required to wear protective clothing and equipment.


⦁    This position requires regular / frequent / occasional domestic / international travel.


IMPORTANT: A resume is required to be considered for this position. If you have not uploaded your resume in your candidate profile, please return to upload field and attach your resume/CV. 


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 20,000 employees within 110 facilities in 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 supported the development of 86% of the drugs approved by the FDA in 2021.


Equal Employment Opportunity

Charles River Laboratories is an Equal Opportunity Employer - all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran or disability status.


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 [email protected] 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

Nearest Major Market: Philadelphia

Job Segment: Biology, Biotech, Database, Toxicology, Pharmaceutical, Science, Technology

2022-11-19 00:00:00

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