2027 Summer Intern - Clinical Pathology

Location: Mattawan, MI, US

2027 Summer Intern - Clinical Pathology

Req ID #

237277

Location

Mattawan, MI, US, 49071

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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

A research intern within the Clinical Pathology discipline is responsible for developing proficiency in the execution of assigned core functions according to protocol, SOP, and GLP regulations. The Clinical Pathology discipline is responsible for the scheduling, setup, processing, data production, QC, and analysis of biological specimens with an emphasis on producing a high-quality outcome. In addition to the basic core functions, research interns may be required to assist and/or execute assigned projects.

The pay range for this position is $20.00 - $23.00 per hour.  Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location

Position is open to anyone, regardless of age, who meets the educational and experience requirements as posted.

Must be eligible to work in the US without requiring a sponsor visa.

Job Description

Essential Duties and Responsibilities

• Perform, document, review, verify all procedures, materials, and results in compliance with regulatory standards as applicable (protocols, methods, SOPs, etc.).
• Embody the behaviors and performance characteristics as described in the CRL DNA
• Develop proficiency in laboratory skills that could include labeling, slide consolidation, and HCC processing.
• Gain familiarity and develop an understanding of the required maintenance surrounding the use of assigned equipment.
• Assist and/or execute assigned tasks.
• Operate laboratory equipment with oversight.
• Assist with the entry and analysis of data associated with assigned task(s).
• Perform all other related duties as assigned.

Minimum Qualifications

Education: HS/GED required. Must be enrolled in an accredited university/collage program, preferably Biology, Clinical Pathology, MLT or MLS.

• Competency required for departmental technical skills.
• Ability to communicate verbally and in writing at all levels inside and outside the organization.
• Basic familiarity with Microsoft Office Suite
• Computer skills, commensurate with Essential Functions, including the ability to learn a validated system.
• Ability to work extended hours beyond normal work schedule to include, but not limited to evenings, weekends, extended shifts, and/or extra shifts, sometimes on short notice.
• Ability to work under specific time constraints.

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.
• While performing the duties of this job, the employee will be required to wear protective clothing which may include goggles, face shield, surgical mask, cap, gloves and scrubs, work with toxic or caustic chemicals, work with biohazards, and/or work near live animals with risk of exposure to allergens and/or zoonotic diseases.
• The employee may be exposed to fumes or airborne particles, unpleasant odors, and/or wet, humid and/or extreme temperature conditions.
• Specific vision abilities required by this job include close vision, color vision, depth perception, and the ability to adjust focus.

Education

No degree required

Physical Requirements

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 improv