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Support Scientist

Charles River Laboratories International Inc (CRL)

Horsham, PA, US, 19044

Support Scientist Req ID #:  142593 Location: 

Horsham, PA, US, 19044 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.

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

Provides administrative support to Study Directors for management of data and preparation of protocol/study plans and study reports and assists with providing requested data/information.  May also assist with management of Quality Assurance (QA) audits. Job Qualifications ESSENTIAL DUTIES AND RESPONSIBILITIES:  

•    Attending study-related and/or department-related meetings to assure understanding of assigned projects including objectives, timelines, and reporting requirements.

•    With guidance from Study Directors, assists in generating drafts Study Plans/Protocols and amendments and may facilitate signature/approval process for study plans/protocols, amendments, and other required forms or documents.

•    Verifies documents against any client-specific requirements indicated in Client Information Database (CID).

•    May assist in initial preparation of animal ethical project review summary.

•    Extract data for preparation of Sponsor updates.

•    Create/generate special tables/graphics as support for Sponsor/Study Director, as needed.  This may be performed in support of toxicology studies and/or as support for PI/IS contributing reports.

•    Assists with drafting of materials & methods sections of reports.

•    Performs Quality Control (QC) of draft reports and Common Technical Documents (CTD).

•    Assists with management of QA audits, may answer QA audit findings and assures necessary corrections as directed by the Study Director.

•    May assist in documentation of deviations from the protocol/study plan or Standard Operating Procedures (SOP).

•    Involved or responsible for tabulation of study data.

•    May help schedule data review meetings.

•    May assembles report (text and data tables) for Study Director review, QA audits, and final report compilation. 

•    May assist in obtaining Sponsor approvals for finalization of documents (e.g., protocols/study plans and/or reports).

•    May assist in documentation of deviations from the study plan/protocol or Standard Operating Procedures (SOP).

•    May attend scientific meetings, conferences or training courses to enhance job and professional skills.

•    Performs all other related duties as assigned.

QUALIFICATIONS:

•    Education: Bachelor’s degree (BA/BS) in Toxicology, Pharmacology or related field - required.  

•    Experience:  No work experience required. 

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. 

Vaccine Mandate

Charles River is a U.S. Federal Contractor.  As a result, we must follow the Presidential Executive Order to mandate vaccinations, and ensure our employees are fully vaccinated against COVID-19 by December 8, 2021.  Our main priority is the wellbeing, health, and safety of our people. We will be requiring proof of vaccination from all employees. 

Anyone with requests for disability-related and/or religious exemptions should contact Talent Acquisition (crrecruitment_US@crl.com) so that information can be provided about the accommodation process at Charles River.

 

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 18,000 employees within 100 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 supported the development of >80% of the drugs approved by the FDA for the past 3 years.

Equal Employment Opportunity

Charles River Laboratories is an Equal Opportunity Employer - M/F/Disabled/Vet.

 

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: Philadelphia

Job Segment: Toxicology, Scientific, Biotech, Scientist, Administrative Assistant, Science, Engineering, Administrative

Job posted: 2022-01-02

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