What are the responsibilities and job description for the Toxicology - Scientific & Management - Technical/Scientific position at Charles River Laboratories?
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
Title: Senior Scientific Associate
Principal Activities / Roles & Responsibilities
- Functions as an independent Study Director in accordance with the applicable GLPs;
- Understands regulations and GLP's as they relate to primary area of focus;
- Understands the study process from proposal to report;
- Oversees and coordinates study conduct (protocol development, technical guidance, and reporting);
- Assists in study planning, scheduling, and execution under the supervision of Sr. Scientist(s)/Scientific Manager;
- Hosts client visits and telephone conferences with support/guidance from Sr. Scientist(s) as needed;
- Effectively communicates with internal and external clients in a manner that generates confidence and builds trust;
- Works on programs of basic complexity;
- Basic knowledge of QA/QC process;
- Interacts with veterinary staff, understands the ethical review process, the 3Rs, and the SD role in animal welfare;
- Gains familiarity with overall project costs and communicates with the technical supervisor as well as the Scientific Manager on issues of staffing and equipment.
- May attend scientific meetings, conferences and training courses to enhance job and professional skills.
Experiences and Background:
At least BSc and relevant work experience/education. Equivalent to 5 years' total experience in relevant area/education.
Job Qualifications
Title: Senior Scientific Associate
Principal Activities / Roles & Responsibilities
- Functions as an independent Study Director in accordance with the applicable GLPs;
- Understands regulations and GLP's as they relate to primary area of focus;
- Understands the study process from proposal to report;
- Oversees and coordinates study conduct (protocol development, technical guidance, and reporting);
- Assists in study planning, scheduling, and execution under the supervision of Sr. Scientist(s)/Scientific Manager;
- Hosts client visits and telephone conferences with support/guidance from Sr. Scientist(s) as needed;
- Effectively communicates with internal and external clients in a manner that generates confidence and builds trust;
- Works on programs of basic complexity;
- Basic knowledge of QA/QC process;
- Interacts with veterinary staff, understands the ethical review process, the 3Rs, and the SD role in animal welfare;
- Gains familiarity with overall project costs and communicates with the technical supervisor as well as the Scientific Manager on issues of staffing and equipment.
- May attend scientific meetings, conferences and training courses to enhance job and professional skills.
Experiences and Background:
At least BSc and relevant work experience/education. Equivalent to 5 years' total experience in relevant area/education.
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.
