Research Associate I, DART

Charles River Laboratories; Ashland (OH); On-site; USD 28,000 - 40,000; Full time

Job summary

Charles River Laboratories is seeking a supervisor to oversee study-related activities for nonclinical studies. You will coordinate scheduling, review protocols, and ensure data is collected and organized in line with SOPs and study plans.

The role requires a minimum of 2 years in a GLP environment, along with a high school diploma or GED. You must be able to organize, prioritize, and work in the United States without visa sponsorship. The pay is $25.00/hr, with location in Ohio.

Qualifications

• Education: High School diploma or General Education Degree (G.E.D.) preferred.
• Experience: 2 years of related experience in a GLP environment.
• 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: Ability to organize, prioritize work and meet deadlines. Computer literacy with word processing, spreadsheet, and data base programs.
• Must be authorized to work in United States without a sponsor visa now or in the future.

Responsibilities

• Coordinates assignments to facilitate scheduling of study-related events on assigned studies (in conjunction with other departments) to ensure protocol requirements are met.
• Review study protocols and provide recommendations to study director/supervisor on technical and logistical aspects of protocol design.
• Assist in preparing responses to both internal and external quality assurance audits.
• Responsible for the accurate preparation and review of study calendars from draft and final protocols and ensuring all protocol-driven activities are accurately scheduled.
• Monitors scientific projects, and the conduct of procedures in accordance with the study protocol, and applicable SOP's.
• Acts as liaison between technical staff, internal departments, and Study Director on assigned studies.
• May perform limited technical activities as needed.
• Coordinate ordering of study equipment and supplies.

Skills

Organize work

Prioritize tasks

Computer skills

Education

High School diploma or GED

Job description

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

BASIC SUMMARY

Supervises and coordinates all study-related activities of research technical staff to ensure compliance with the protocol and applicable SOP's and maintains the raw data for nonclinical studies.

Essential Duties And Responsibilities

• Coordinates assignments to facilitate scheduling of study-related events on assigned studies (in conjunction with other departments) to ensure protocol requirements are met.
• Scope of work includes studies of all duration, size, and complexity generally with some supervision.
• Review study protocols and provide recommendations to study director/supervisor on technical and logistical aspects of protocol design.
• Assist in preparing responses to both internal and external quality assurance audits.
• Responsible for the accurate preparation and review of study calendars from draft and final protocols and ensuring all protocol-driven activities are accurately scheduled.
• Monitors scientific projects, and the conduct of procedures in accordance with the study protocol, and applicable SOP's.
• Acts as liaison between technical staff, internal departments, and Study Director on assigned studies.
• Responsible for the preparation of study notebooks, organization of study data, timely (including daily) review of all study-related data generated by Technical Operations (according to established metrics) and submission of study notebook to Quality Assurance.
• May perform limited technical activities as needed.
• Participate in the team meetings.
• Coordinate ordering of study equipment and supplies.
• Perform all other related duties as assigned.

The pay for this position is $25.00/hr. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

Qualifications

Job Description

• Education: High School diploma or General Education Degree (G.E.D.) preferred.
• Experience: 2 years of related experience in a GLP environment. Experience with research and investigative procedures, techniques, and literature.
• 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: Ability to organize, prioritize work and meet deadlines. Computer literacy with word processing, spreadsheet, and data base programs.
• Must be authorized to work in United States without a sponsor visa now or in the future.

Physical Demands

• While performing the duties of this job, the employee is regularly required to talk, hear, and type at a computer.
• Specific vision abilities required by this job include close vision and the ability to adjust focus.
• Employees working with animals must be able to lift, move and/or hold up to 40 pounds; this includes equipment and large and small animals.

Work Environment

• While performing the duties of this job, the employee occasionally wears protective clothing (goggles, face shield, surgical mask, cap, gloves, scrubs, boots).
• Occasionally works with biohazards and sharps.
• Occasionally works with live animals (small, medium and/or large) with risk of exposure to allergens and/or zoonotic diseases.
• While performing the duties of this job the employee is occasionally exposed to fumes or airborne particles, unpleasant odors, and wet, humid and/or extreme temperature conditions.
• The noise level in the work environment is usually low and occasionally moderate.

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, and 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.

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