Job Summary
We are seeking a Research Scientist 1 for our Safety Assessment site located Shrewsbury.
The Research Scientist 1 will serve as a scientist in the conduct of assigned in-vivo preclinical efficacy studies of basic to moderate complexity, to include study management, interpretation, preparation of protocols/study plans, coordination with technical teams, reporting of study data, and assuming the compliance of these projects.
ESSENTIAL DUTIES AND RESPONSIBILITIES:
- Serve as a Study Director in the direction and execution of assigned preclinical pharmacology studies. Understand the study process from proposal to report. Prepares protocols and study plans.
- Participate in and coordinate all phases of study, to include protocol development, technical guidance and training.
- Generate high-quality protocols, amendments and reports for assigned studies.
- Effectively communicates with internal and external clients in a manner that generates confidence and builds trust. Function as main contact for sponsor interaction related to assigned studies.
- Basic knowledge of Quality Assurance (QA)/Quality Control (QC) process. Interacts with veterinary staff, understands the IACUC process, and understands the Study Director role in animal welfare.
- Understands the importance of overall project costs and communicates with the technical supervisor as well as the Scientific Manager on issues of staffing and equipment. May participate in proposal development.
- Assists with mentoring of less experienced staff and may assist with training of scientific/senior scientific associate, as needed.
- May attend scientific meetings, conferences and training courses to enhance job and professional skills. Gains experience and begins to develop an area of expertise.
- Perform all other related duties as assigned
The following are minimum qualifications related to the Research Scientist 1 position:
- Education: Bachelor's degree (B.S./B.A.) or equivalent in a scientific related discipline. Related Master's degree (M.S./M.A.) or PhD/DVM preferred.
- Experience: Minimum of 6 to 7 years related experience in the contract research, academic, or pharmaceutical industry.
- 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.
- Other: Understanding of regulatory requirements of study types assigned, as well as Testing Facility SOPs and the Good Laboratory Practices (GLPs), as appropriate. Effective written and verbal communication skills. Ability to handle multiple projects, prioritize work and meet deadlines. Proficiency in the use of standard software including Microsoft Excel, Word, Powerpoint, etc. and with standard laboratory calculations.
About Discovery
Discovery from Charles River is industry-proven in the successful development of novel therapies, with over 320 patents and 74 preclinical drug candidates delivered to our sponsors in the past 17 years. Backed by more than 650 scientists, our comprehensive, integrated portfolio employs the latest technology and platforms to provide chemistry, biology, and pharmacology services that support clients from the earliest stages of hit identification all the way through to IND. Our client-focused, collaborative approach creates true partnerships that anticipate challenges, overcome obstacles, and move us forward together on the journey of getting new drugs to market.
With over 14,000 employees within 80 facilities in 20 countries around the globe, we are strategically positioned to coordinate worldwide resources and apply multidisciplinary perspectives in resolving our clients unique challenges. Our client base includes global pharmaceutical companies, biotechnology companies, government agencies and hospitals and academic institutions around the world. And in 2018, revenue increased by 22% to $2.27 billion from $1.86 billion in 2017.
At Charles River, we are passionate about our role in improving the quality of peoples 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 ~85% of the drugs approved by the FDA in 2018.
Equal Employment Opportunity
Charles River Laboratories is an Equal Opportunity Employer - M/F/Disabled/Vet