Research Analyst I - Formulations
About the role
SHIFT SCHEDULE: Friday – Monday 6:00 AM-2:30 PM
TRAINING SCHEDULE: Monday to Friday 6:00 AM-2:30 PM for first 12 weeks of employment
HOURLY RATE: The pay rate for this position is $23.50/hr + 10% shift differential on Saturday and Sunday. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.
Job Requirements
- Education: Associate’s degree (A.A./A.S.) or equivalent in chemistry/pharmacy or related discipline preferred. Bachelor’s degree (B.A./B.S.) desired.
- Experience: 3-5 years related experience in formulations. Six months to one year in a leadership role desired.
- Other: A mathematical aptitude required. Demonstrated leadership and word processing skills. Effective written and verbal skill
Workplace Requirements
- While performing the duties of this job, the employee must be able to perform general office and/or laboratory procedures, which require, talking, hearing, standing, or sitting for long periods of time, typing/entering data into a computer, using appropriate instruments, reaching with hands and arms, and wearing safety equipment (PPE) according to OSHA regulations and company standards.
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 300 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.
Equal Employment Opportunity
Charles River is an equal opportunity employer and is committed to providing equal employment opportunities for all qualified applicants and employees without regard to race, color, sex, religion, national origin, ancestry, age, mental or physical disability, family status, pregnancy, military or veteran status, or any other characteristic protected by federal, state, or local laws.