Research Support Specialist
1 month ago
For over 75 years, Charles River Laboratories has been dedicated to aiding in the discovery, development, and safe production of innovative drug therapies. By becoming part of our organization, you will significantly contribute to the health and wellness of individuals worldwide. Regardless of your background in life sciences, finance, IT, sales, or other fields, your expertise will be vital to our mission. In return, we are committed to helping you cultivate a fulfilling career.
Position OverviewAs a Support Scientist, your role will involve providing both administrative and scientific assistance to Study Directors, focusing on data management and the preparation of study plans and reports. You will also play a crucial role in facilitating Quality Assurance (QA) audits.
Primary ResponsibilitiesYour key responsibilities will include:
- Participating in study-related meetings to ensure clarity on project objectives, timelines, and reporting requirements.
- Assisting in drafting study plans and amendments.
- Contributing to the initial preparation of animal ethics project review summaries.
- Extracting data for sponsor updates.
- Reviewing and processing specialty departmental data.
- Creating and generating specialized tables and graphs.
- Drafting and conducting quality control (QC) on main report materials and methods, as well as common technical documents (CTD).
- Assisting in managing QA audits by addressing findings and implementing necessary corrections.
If you possess the following qualifications, we will provide training for the remaining skills:
- Education: A minimum of a Bachelor's degree (BA/BSc) in a scientific discipline or equivalent.
- Proficiency in English (both spoken and written).
- Competence in Microsoft Word and Excel.
- Experience in a GLP environment and/or preclinical toxicology is advantageous.
- An equivalent combination of education and experience may be accepted as a substitute for the specific qualifications listed above.
- Competitive benefits from the start, covering up to 85% of health and dental premiums.
- Paid training for professional development.
- Employee and family assistance programs.
- Access to telemedicine services with various health professionals.
- Three weeks of vacation and five sick/personal days annually.
- A variety of social activities.
If you are passionate about contributing to the health of communities both nationally and globally, we encourage you to consider this opportunity.
About Charles River Laboratories
Charles River is an early-stage contract research organization (CRO) that has built 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. Our extensive range of products and services enables clients to create a flexible drug development model, reducing costs and enhancing productivity to accelerate time to market.
With over 20,000 employees across 110 facilities in more than 20 countries, we are strategically positioned to leverage global resources and multidisciplinary perspectives to address our clients' unique challenges. Our clientele includes global pharmaceutical companies, biotechnology firms, government agencies, hospitals, and academic institutions worldwide.
At Charles River, we are dedicated to improving the quality of life for people everywhere. Our mission, commitment to excellent science, and strong sense of purpose guide our daily work, knowing that our efforts contribute to the health and well-being of many across the globe.
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.
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