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Science Coordinator Jobs in Reno, NV (NOW HIRING)

In addition, they must be able to perform all the duties as outlined in the Clinical Lab Scientist ... The Lab Program Coordinator will maintain organization of workload, complete quality control ...

Lab Program Coordinator

Reno, NV · On-site

$46.08 - $64.52/hr

In addition, they must be able to perform all the duties as outlined in the Clinical Lab Scientist ... The Lab Program Coordinator will maintain organization of workload, complete quality control ...

In addition, they must be able to perform all the duties as outlined in the Clinical Lab Scientist ... The Lab Program Coordinator will maintain organization of workload, complete quality control ...

Physician Scheduling Coordinator

Reno, NV · On-site

$17.75 - $22.50/hr

Position Purpose This position is responsible for coordinating outpatient and/or facility physician ... Bachelors of Art or Bachelor of Science in Healthcare is preferred. Experience: 2-3 years of ...

Physician Scheduling Coordinator

Reno, NV · On-site

$17.75 - $22.50/hr

Position Purpose This position is responsible for coordinating outpatient and/or facility physician ... Bachelors of Art or Bachelor of Science in Healthcare is preferred. Experience: 2-3 years of ...

Physician Scheduling Coordinator

Reno, NV · On-site

$21.11 - $29.56/hr

Position Purpose This position is responsible for coordinating outpatient and/or facility physician ... Bachelors of Art or Bachelor of Science in Healthcare is preferred. Experience: 2-3 years of ...

Physician Scheduling Coordinator

Reno, NV · On-site

$17.75 - $22.50/hr

Position Purpose This position is responsible for coordinating outpatient and/or facility physician ... Bachelors of Art or Bachelor of Science in Healthcare is preferred. Experience: 2-3 years of ...

Physician Scheduling Coordinator

Reno, NV · On-site

$21.11 - $29.56/hr

Position Purpose This position is responsible for coordinating outpatient and/or facility physician ... Bachelors of Art or Bachelor of Science in Healthcare is preferred. Experience: 2-3 years of ...

Physician Scheduling Coordinator

Reno, NV · On-site

$17.75 - $22.50/hr

Position Purpose This position is responsible for coordinating outpatient and/or facility physician ... Bachelors of Art or Bachelor of Science in Healthcare is preferred. Experience: 2-3 years of ...

Physician Scheduling Coordinator

Reno, NV · On-site

$17.75 - $22.50/hr

Position Purpose This position is responsible for coordinating outpatient and/or facility physician ... Bachelors of Art or Bachelor of Science in Healthcare is preferred. Experience: 2-3 years of ...

Nurse Residency Program Coordinator

Reno, NV · On-site

$43.89 - $61.44/hr

The incumbent coordinates the nurse residency program for newly hired nurses across the enterprise ... Master of Science degree in Nursing with appropriate specialty track preferred. Experience: Minimum ...

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Showing results 1-20

Science Coordinator information

See Reno, NV salary details

$12

$22

$33

How much do science coordinator jobs pay per hour?

As of Jul 15, 2026, the average hourly pay for science coordinator in Reno, NV is $22.55, according to ZipRecruiter salary data. Most workers in this role earn between $18.46 and $24.90 per hour, depending on experience, location, and employer.

What is the difference between Science Coordinator vs Science Technician?

AspectScience CoordinatorScience Technician
Required CredentialsBachelor's degree in science or related field; sometimes additional certificationsAssociate's degree or technical certification in science or laboratory work
Work EnvironmentEducational institutions, research labs, or science programsLaboratories, research facilities, or industrial settings
Employer & Industry UsageSchools, universities, research organizationsLaboratories, manufacturing, research institutions
Common Search & Comparison IntentUnderstanding roles in science education and coordinationTechnical support and laboratory work roles

The main difference between a Science Coordinator and a Science Technician lies in their responsibilities and qualifications. Science Coordinators typically oversee science programs, plan curricula, and coordinate activities, requiring a higher level of education and organizational skills. Science Technicians focus on supporting laboratory operations, conducting experiments, and maintaining equipment, often with technical certifications. Both roles are essential in scientific settings but serve different functions within the industry.

What does a Science Coordinator do?

A Science Coordinator oversees the development and implementation of science curriculum and educational programs within schools or districts. They support teachers by providing resources, organizing professional development, and ensuring that science instruction aligns with standards. Science Coordinators may also evaluate teaching methods, facilitate collaboration among educators, and help integrate new technologies or scientific advancements into the classroom. Their goal is to improve science teaching and learning outcomes for students.

How does a Science Coordinator typically collaborate with teachers and school administrators to improve science curriculum?

A Science Coordinator works closely with teachers to provide guidance on implementing science curriculum, offering support through professional development, resource sharing, and modeling effective instructional strategies. They also collaborate with school administrators to align science programs with district or state standards and to analyze student performance data for ongoing improvement. This role often involves facilitating communication between staff, organizing workshops, and ensuring that science instruction remains current and effective across grade levels.

What are the key skills and qualifications needed to thrive as a Science Coordinator, and why are they important?

To thrive as a Science Coordinator, you need a strong background in science education, curriculum development, and instructional leadership, often supported by a teaching credential and advanced degree. Familiarity with educational technology platforms, data analysis tools, and state or national science standards is typically required. Strong organizational, communication, and leadership skills help in managing teams and fostering collaboration among teachers and stakeholders. These skills are crucial for ensuring high-quality science instruction and aligning educational practices with current standards and student needs.
What are the most commonly searched types of Science jobs in Reno, NV? The most popular types of Science jobs in Reno, NV are:
Data Coordinator

$22/hr

Full-time

Medical, Retirement, PTO

Posted 14 days ago


Charles River Laboratories rating

8.3

Company rating: 8.3 out of 10

Based on 93 frontline employees who took The Breakroom Quiz

18th of 74 rated pharmaceutical


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

We are seeking a Data Coordinator at our Safet Assessment Facility in Reno, NV.

BASIC SUMMARY:  

Responsible for coordinating the data table process to produce quality, on-time report components (tables, graphs, etc.) and supplemental report components (glossaries, code pages, etc.); providing support for internal and external customers; and independently prioritizing workload. The individual in this role serves as a mentor for new employees and contributes expertise to process improvement initiatives.

 

ESSENTIAL DUTIES AND RESPONSIBILITIES:  

  • From validated systems and other data sources, generate and perform review of report components, such as tables, and other supplemental report components according to the data, protocol, format and compliance requirements.
  • Receive, review, and accept proof corrections and make recommended corrections as appropriate.
  • Independently evaluate and prioritize study work (scheduled and unscheduled) to coordinate the document creation process and data-entry process with the study team.
  • Provide table status updates, review data and raise data issues; collaborate with members of the study team to get resolution of data issues that affect document generation.
  • Handle special customer requests, such as expedited timelines, preliminary tables, and custom formats.
  • Respond to, clarify, and evaluate Quality Assurance Observations with the Quality Assurance staff; review and complete Corrective Action Preventative Action events; and address compliance issues.
  • Carry out all work in accordance with Operating Procedures and other relevant codes of practice/standards.
  • Train and serve as a mentor for new employees in relevant areas.
  • Serve as a subject matter expert within a product line or for a departmental process.
  • Contribute expertise to focus/process improvement groups within reporting department.
  • Perform other related duties, as assigned.
Job Description

MINIMUM QUALIFICATIONS:

  • Education: High School Diploma or G.E.D. required. 
  • Experience: 1 or more years related experience.
  • 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:  Demonstrated technical competence and ability to prioritize daily tasks. 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 duties and responsibilities, including the ability to learn a validated system. Ability to work under specific time constraints.

PREFERRED QUALIFICATIONS:

  • Education: Bachelor’s (B.A./B.S.) degree in relevant field preferred.
  • Experience: Contract research organization experience preferred.

Starting Wage: $22

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 crrecruitment_US@crl.com. 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.


What Charles River Laboratories employees say

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About Charles River

Sourced by ZipRecruiter

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 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 supported the development of 86% of the drugs approved by the FDA in 2021.

Industry

Scientific research and development services

Company size

10,000+ Employees

Headquarters location

Wilmington, MA, US

Year founded

1947