Research Scientist I, Analytical Chemistry

Charles River; Reno (NV); Presencial; USD 90.000 - 95.000; Tempo integral

Resumo da vaga

Charles River is seeking an experienced Research Scientist (Analytical Chemistry) for our Safety Assessment site in Reno, NV. The role involves conducting preclinical and clinical studies, study direction under GLP, data interpretation and reporting, and ensuring regulatory compliance.

You will lead sponsor interactions and provide scientific guidance to staff. Ideal candidates have 3–5 years in CRO/academic/pharmaceutical settings, strong analytical skills (HPLC, SoloVPE, UV-Vis, CE, iCIEF),

Qualificações

• Bachelor's degree in a scientific field; MS or PhD preferred.
• 3–5 years of related CRO/academic/pharmaceutical experience.
• Expert in analytical techniques (HPLC, SoloVPE, UV-Vis, CE, iCIEF).
• Knowledge of GLP and regulatory study requirements.
• Strong written and verbal communication; able to manage multiple projects.

Responsabilidades

• Conduct preclinical/clinical studies of basic to moderate complexity with study management and data reporting.
• Act as study director ensuring GLP compliance and study direction.
• Coordinate study planning with relevant departments.
• Generate protocols, amendments, and study reports.
• Review and present data; provide scientific guidance to staff.
• Interface with sponsors for study planning, scheduling, and proposals.

Conhecimentos

Analytical techniques

Study management

Regulatory compliance

Communication skills

MS Office (Excel/Word/PowerPoint)

Formação

Bachelor's degree in science

MS/PhD preferred

Ferramentas

HPLC

SoloVPE

UV-Vis

CE

iCIEF

Descrição da vaga

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.

Job Overview

We are seeking an experienced Research Scientist (Analytical Chemistry) for our Safety Assessment site located in Reno, NV. They will serve as a scientist in the conduct of assigned preclinical and clinical research studies of basic to moderate complexity, to include study management, interpretation and reporting of study data, and assuring the regulatory compliance of these projects.

Job Description

• Serve as a scientist in the conduct of assigned preclinical and clinical research studies of basic to moderate complexity, to include study management, interpretation and reporting of study data, and assuring the regulatory compliance of these projects.
• Serve as a study director in the direction and execution of assigned studies in compliance with GLP regulations as they apply to the conduct of nonclinical research.
• Participate in and coordinate all phases of the study planning process with appropriate departments.
• Generate high-quality protocols, amendments, and reports appropriate for assigned studies.
• Review, interpret, integrate, and present data on assigned studies, using the assistance of senior scientific staff as appropriate.
• Function as contact for the planning and execution of sponsor interaction related to assigned studies, including proposal management and study scheduling, conduct and reporting.Provide technical and scientific guidance to the research staff.
• Expert in several analytical techniques (e.g. HPLC, SoloVPE, UV-Vis, subvisible particles, CE, iCIEF).
• Attend scientific meetings, conferences and training courses to enhance job and professional skills.
• Perform all other related duties as assigned.

The pay for this position is between $90,000-95,000/yr. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

Experience And Education Requirements

• Bachelor's degree (B.S./B.A.) or equivalent in a scientific related discipline. Related Master's degree (M.S./M.A.) or PhD preferred.
• Minimum of 3 to 5 years related experience in the contract research, academic, or pharmaceutical industry.
• Expert in several analytical techniques e.g. HPLC, SoloVPE, UV-Vis, subvisible particles, CE, iCIEF.
• An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.
• 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 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.

With over 20,000 employees within 110 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 worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

We’re committed to providing benefits that elevate your quality of life. Based on your position these may include:

• bonus/incentives based on performance
• 401K
• paid time off
• stock purchase program
• Health and wellness coverage
• employee and family wellbeing support programs
• work life balance flexibility

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.

It is unlawful in some states (including Massachusetts) to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.

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 [e-mail]. 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.