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Study Coordinator Jobs in Colorado (NOW HIRING)

Inotiv

Study Coordinator

Westminster, CO · On-site

$26 - $33/hr

Communicate with other coordinators to schedule study activities * Ensure creation of data sheets * Confirm laboratory math for test article and disease induction formulation * Communicate with ...

The US Oncology Network

Study Coordinator

Denver, CO · On-site

$60K - $75K/yr

Overview Rocky Mountain Cancer Centers, Colorado's largest and most comprehensive provider of cancer care has an exciting opportunity for an experienced Research Study Coordinator in Denver Bring ...

Inotiv

Study Coordinator

Boulder, CO · On-site

$27 - $34/hr

The Study Coordinator reports to the Study Coordinator Supervisor within the In Vivo Department with responsibilities centered around supporting all functions of the preclinical study process. The ...

Inotivco

Study Coordinator

Westminster, CO · On-site

$26 - $33/hr

Communicate with other coordinators to schedule study activities * Ensure creation of data sheets * Confirm laboratory math for test article and disease induction formulation * Communicate with ...

Inotivco

Study Coordinator

Boulder, CO · On-site

$34/hr

The Study Coordinator reports to the Study Coordinator Supervisor within the In Vivo Department with responsibilities centered around supporting all functions of the preclinical study process. The ...

The US Oncology Network

Study Coordinator

Denver, CO

$60K - $75K/yr

Overview Rocky Mountain Cancer Centers, Colorado's largest and most comprehensive provider of cancer care has an exciting opportunity for an experienced Research Study Coordinator in Denver Bring ...

Inotiv

Study Director

Westminster, CO · On-site

Informs Live Phase Study Coordinator of decisions to initiate studies and thereby proceed with ordering animals and necessary study supplies * Ensures all research technicians are properly trained to ...

Inotivco

Study Director

Westminster, CO · On-site

Informs Live Phase Study Coordinator of decisions to initiate studies and thereby proceed with ordering animals and necessary study supplies * Ensures all research technicians are properly trained to ...

Inotiv, Inc.

Study Director

Westminster, CO · On-site

$80 - $120/hr

Informs Live Phase Study Coordinator of decisions to initiate studies and thereby proceed with ordering animals and necessary study supplies* Ensures all research technicians are properly trained to ...

Medpace, Inc.

CO · Hybrid

$75K - $110K/yr

Medpace provides Project Coordinators a 4-6 week training program that incorporates a virtual and ... Manage study supplies; * Create and maintain project timelines; and * Coordinate project meetings ...

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All JobsStudy JobsStudy Coordinator JobsStudy Coordinator Jobs in Colorado

Study Coordinator information

See Colorado salary details

$23.1K

$57.7K

$84.6K

How much do study coordinator jobs pay per year?

As of Aug 8, 2026, the average yearly pay for study coordinator in Colorado is $57,679.00, according to ZipRecruiter salary data. Most workers in this role earn between $46,300.00 and $65,700.00 per year, depending on experience, location, and employer.

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

To thrive as a Study Coordinator, you need a solid understanding of clinical research protocols, regulatory compliance, and data management, usually backed by a bachelor’s degree in a science or health-related field. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) platforms, and Good Clinical Practice (GCP) certification is typically required. Strong organizational skills, attention to detail, and effective communication help you manage study logistics and collaborate with research teams and participants. These skills ensure that studies are conducted ethically, efficiently, and in accordance with regulatory standards.

What is a study coordinator?

A study coordinator works in a clinical research environment. In this position, your job duties are to oversee the day-to-day operations of a given study under the guidance of a research director. You direct tests, ensure all research is done according to ethical standards, and ensure the comfort and safety of subjects. As a study coordinator, you also ensure all patients provide informed consent prior to participation. Overall, your responsibility is to provide a safe environment for the study. To be a study coordinator, the qualifications are usually a bachelor’s degree or an RN degree. You typically need several years of experience in a clinical setting, and you must demonstrate skills in research.

What are some common challenges study coordinators face when managing multiple clinical trials simultaneously?

Study Coordinators often juggle several clinical trials at once, each with its own protocols, timelines, and regulatory requirements. Keeping track of participant enrollment, data collection, and compliance across different studies can be demanding and requires strong organizational skills. Effective communication with investigators, sponsors, and other team members is crucial to prevent errors, ensure deadlines are met, and maintain the quality of study data. Using robust tracking systems and prioritizing tasks can help manage these challenges efficiently.

What is the difference between Study Coordinator vs Research Assistant?

AspectStudy CoordinatorResearch Assistant
Required CredentialsTypically a bachelor's degree in health sciences, biology, or related fieldOften a bachelor's degree or current student in a related field
Work EnvironmentClinical research settings, hospitals, or research institutionsLaboratories, research centers, or clinical sites
Employer & Industry UsageUsed by hospitals, universities, and research organizationsCommonly employed in academic and research institutions
Common Search & Comparison IntentUnderstanding roles, responsibilities, and qualificationsLearning about entry-level research roles and support tasks

The Study Coordinator and Research Assistant roles share similarities in working within research environments and requiring related educational backgrounds. However, Study Coordinators typically have more responsibilities in managing study protocols and participant coordination, while Research Assistants focus on supporting research activities and data collection. Both roles are essential in advancing clinical research and often work closely together in research projects.

More about Study Coordinator jobs
What are the most commonly searched types of Study jobs in Colorado? The most popular types of Study jobs in Colorado are:
What are popular job titles related to Study Coordinator jobs in Colorado? For Study Coordinator jobs in Colorado, the most frequently searched job titles are:
What job categories do people searching Study Coordinator jobs in Colorado look for? The top searched job categories for Study Coordinator jobs in Colorado are:
What cities in Colorado are hiring for Study Coordinator jobs? Cities in Colorado with the most Study Coordinator job openings:
Study Coordinator jobs near you
Infographic showing various Study Coordinator job openings in Colorado as of August 2026, with employment types broken down into 1% As Needed, 82% Full Time, 14% Part Time, 1% Temporary, and 2% Contract. Highlights an 83% Physical, 1% Hybrid, and 16% Remote job distribution, with an average salary of $57,679 per year, or $27.7 per hour.

Study Coordinator

Inotiv

Westminster, CO • On-site

$26 - $33/hr

Full-time

Medical, Dental, Retirement, PTO

Posted 13 days ago

Inotiv rating

8.2

Company rating: 8.2 out of 10

Based on 21 frontline employees who took The Breakroom Quiz

29th of 73 rated research

Job description

Responsibilities and Duties
Corporate
  • Follow all SOPs and other applicable company policies and procedures
  • Maintain confidential information

General
  • Interact and communicate with clients, vendors, other employees, and the community in a professional manner
  • Support and participate in company initiatives as directed
  • Maintain thorough knowledge of facility SOPs, policies, protocols, etc.
  • Adhere to all safety regulations and procedures
  • Provide assistance or support to other Inotiv sites as necessary
  • Perform other duties as assigned

Specific
  • Maintain and submit study initiation materials
  • Order all applicable supplies for studies
  • Communicate with other coordinators to schedule study activities
  • Ensure creation of data sheets
  • Confirm laboratory math for test article and disease induction formulation
  • Communicate with formulations team regarding timeline and materials needed
  • Assist with in-life study conduct, as needed, and as trained
  • Complete training requirements as assigned and maintain appropriate training documentation
  • Perform periodic review of all applicable SOPs to ensure accuracy and confirm procedures are being performed according to SOPs. Participate in SOP writing, reviews, and revisions, as needed
  • Maintain compliance with all policies and procedures
  • Ensure compliance with USDA, AAALAC, OLAW, GLPs and other applicable regulations
  • Perform quality checks, reviews, and formatting on all Inotiv documents (e.g. protocols, amendments, deviations, reports, tables, etc.)
  • Develop and maintain study protocol, report, and data table master templates
  • Provide back-up support for Study Directors as needed
  • Aid in protocol and any protocol amendment or deviation preparation and distribution
  • Prepare and review raw data collection forms and review for adherence to protocol, both prior to study start and after study completion
  • Review raw data collection and in-life study conduct
  • Assist to prepare a complete study file for archival following finalization of report
  • Assist to ensure that study samples and test articles are shipped appropriately, on schedule, and documented in the study file
  • Perform other duties as assigned

Position Requirements
Education and experience
  • At a minimum, the Study Coordinator must have a Bachelor's degree in life sciences or other directly related field or degree with comparable coursework and a minimum of three years in a relevant pharmaceutical setting
  • The Study Coordinator must have a minimum of one year experience with animals and animal handling

Skills and abilities
  • A working knowledge and awareness of general laboratory procedures
  • Customer focused, results driven, communicative, and collaborative enabling effective customer satisfaction, including problem solving, fostering positive relationships, and proactive communication
  • Ability to adhere to and manage in accordance with the Code of Federal Regulations procedures
  • Experience in the use of computer software applications (e.g., Word, Outlook, Excel)
  • Possess strong skills for editing the format, style and language of draft protocols, spreadsheets and reports
  • Excellent written and verbal communication skills
  • An attitude for quality, an eye for detail and the ability to read and follow written instructions
  • Ability to interact with scientific staff at all levels

Performance Requirements
General
  • Ability to read, write, speak, and understand English
  • Able and willing to work a flexible schedule according to study needs

Physical activity
  • Moderate physical activity:
    • Prolonged periods of sitting at a desk and working on a computer
    • May occasionally lift and/or move objects
  • Able to wear PPE (Personal Protection Equipment) as required

Working Conditions
  • Work is normally performed in a typical interior office or laboratory environment
  • Work may require use of PPE due to exposure to potentially dangerous materials and situations
  • Noise level is usually moderate as commensurate with a typical office environment

Salary Range: $26.00-$33.00 per hour, adjusted according to the level of the role and the candidate's relevant experience and/or education. Salary will be commensurate with experience and responsibilities.
Benefits: Health and dental coverage, short- and long-term disability, paid time off, paid parental leave, 401(k), and more.
Position Status: Open until filled.
#LI-JM1
#LI-Onsite
*This position could be offered at different levels for candidates who qualify with a combination of advanced levels of education and/or years of experience. The salary range will adjust along with the level of the role to match the person's relevant experience and/or education level.
Inotiv is a growing contemporary drug discovery and development company where we "Play to Win" in an industry rich with opportunity. Together, we face challenges and together we win in the delivery of world-class drug discovery and development solutions that impact the health and well-being of people all over the world. There's an opportunity for everyone at all phases of a career, each individual's unique skill set has an impact on the work we conduct. If you have the talent and desire to impact the quality of people's lives, we have the career opportunities to make it happen. Join us in embracing research and science to impact the health and well-being of people all over the world.
Salary will be commensurate with experience and responsibilities. Benefits include health and dental coverage, short- and long-term disability, paid time off, paid parental leave, 401K, and more!
Inotiv is an Equal Opportunity Employer. It is our policy to provide a fair and equal employment opportunity to all persons, regardless of age, race, color, religion, sex, gender, gender identity, gender expression, sexual orientation, genetic information, disability, national origin, veteran status, or any other basis prohibited by law. This policy governs all aspects of employment, including selection, job assignment, compensation, discipline, termination and access to benefits and training.

What Inotiv employees say

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About Inotiv

Sourced by ZipRecruiter

Industry

Scientific research and development services

Company size

201 - 500 Employees

Headquarters location

West Lafayette, IN, US

Year founded

1974

Social media

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