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Clinical Trial Operations Jobs in Colorado (NOW HIRING)

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Senior Clinical Research Associate

Denver, CO · On-site

$110K - $138K/yr

Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements ... trial operations. Your Profile: * Advanced degree in a relevant field such as life sciences ...

Clingroup

Clinical Study Monitor-Animal Health

Fort Collins, CO · Remote

$33.25 - $45.25/hr

Collaborate with the team members to support smooth trial operations and successful study outcomes ... Solid understanding of clinical monitoring processes, including site initiation, routine monitoring ...

CPC

Clinical Operations Manager II

Aurora, CO · Remote

$71K - $88K/yr

Oversee trial-related activities. * Track and approve vendor payments. * Provide expert advice in ... study assigned Clinical Operations Manager and the Head of Endpoint and Specialty Services.

CPC

Sr. Clinical Operations Manager

Aurora, CO · On-site +1

Oversee clinical operations management activities when delegated to a Clinical Trial Manager (CTM). For single-site or smaller multi-center studies in which these activities are not delegated to a ...

Syneos Health, Inc.

Medical Science Liaison

Denver, CO · On-site

$190 - $210/hr

Partner with Clinical Development, Clinical Operations, CRO partners, and investigative sites to support effective study startup, protocol understanding, and trial execution. * Execute nonpromotional ...

Syneos Health

Medical Science Liaison

Denver, CO · On-site

$190 - $210/hr

Partner with Clinical Development, Clinical Operations, CRO partners, and investigative sites to support effective study startup, protocol understanding, and trial execution. * Execute nonpromotional ...

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Clinical Trial Operations information

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$18

$42

$73

How much do clinical trial operations jobs pay per hour?

As of Sep 3, 2026, the average hourly pay for clinical trial operations in Colorado is $42.05, according to ZipRecruiter salary data. Most workers in this role earn between $33.89 and $46.25 per hour, depending on experience, location, and employer.

What is a clinical trial operations?

A Clinical Trial Operations job involves overseeing the planning, execution, and management of clinical trials to ensure they comply with regulatory guidelines and study protocols. Professionals in this role coordinate with investigators, sponsors, and regulatory agencies to ensure trials run smoothly and efficiently. They manage timelines, budgets, patient recruitment, data collection, and compliance with ethical and legal standards. Their ultimate goal is to ensure the trial produces reliable data while prioritizing patient safety.

What are the typical daily responsibilities in clinical trial operations?

A clinical trial operations professional oversees the planning, implementation, and management of clinical research studies. Daily tasks often include coordinating study timelines, monitoring site performance, ensuring adherence to regulatory requirements, managing study documentation, and communicating with trial sites and sponsors. The role also involves addressing operational issues quickly and adjusting plans as needed to keep the trial on track. This position usually works closely with principal investigators, data managers, regulatory teams, and sponsors, making collaboration and communication essential for success.

What are the key skills and qualifications needed to thrive in clinical trial operations?

To thrive in Clinical Trial Operations, you typically need a background in life sciences or healthcare, strong project management abilities, and familiarity with clinical research protocols and regulatory guidelines. Experience with clinical trial management systems (CTMS), electronic data capture (EDC) platforms, and certifications like GCP (Good Clinical Practice) are often required. Excellent organizational, communication, and problem-solving skills help you collaborate effectively with cross-functional teams and manage complex study logistics. These competencies are crucial to ensuring clinical trials run smoothly, efficiently, and in compliance with industry standards.

What are the most commonly searched types of Clinical Trial Operations jobs in Colorado?

The most popular types of Clinical Trial Operations jobs in Colorado are:

What are popular job titles related to Clinical Trial Operations jobs in Colorado?

For Clinical Trial Operations jobs in Colorado, the most frequently searched job titles are:

What job categories do people searching Clinical Trial Operations jobs in Colorado look for?

The top searched job categories for Clinical Trial Operations jobs in Colorado are:

Clinical Trial Operations jobs near you
Infographic showing various Clinical Trial Operations job openings in Colorado as of August 2026, with employment types broken down into 1% As Needed, 83% Full Time, 11% Part Time, 2% Temporary, 2% Contract, and 1% Nights. Highlights an 93% Physical, 3% Hybrid, and 4% Remote job distribution, with an average salary of $87,454 per year, or $42 per hour.

Consultant, Clinical Supplies Management, Biopharma, Global Trials

Eliassen Group

Almont, CO • On-site

Other

Medical, Dental, Vision, Life, Retirement

Posted 15 days ago

Job description

Description:
CONTEXT & INITIATIVE DESCRIPTION
Our BioPharma Client is seeking a Consultant, Clinical Supplies Management to support the planning and execution of global Phase I-III clinical trials. This critical Consultant will play a key role in ensuring the timely availability, packaging, distribution, and ongoing management of clinical trial supplies across sites and depots.
The ideal candidate will have strong clinical supply and trial operations experience, excellent cross-functional communication skills, and the ability to coordinate effectively across internal teams, vendors, logistics providers, and clinical sites.
This role will report into our client's Head of Clinical Supplies.
Responsibilities:
DUTIES/EXPECTATIONS:
  • Lead day-to-day operations related to clinical trial inventory, packaging, logistics, and distribution
  • Support forecasting and development of monthly supply and demand requirements to ensure clinical sites have the materials necessary to meet study needs
  • Develop and support supply planning and distribution strategies based on study requirements and enrollment forecasts
  • Assist with the management and distribution of ancillary clinical trial supplies as needed
  • Manage the translation of required clinical trial materials and coordinate review and approval with appropriate functions
  • Work cross-functionally with Clinical, Finance, Quality, Regulatory, and other relevant stakeholders to ensure effective communication and execution
  • Manage and/or oversee Interactive Response Technology (IRT) activities related to clinical supply management
  • Support vendor management and coordination to ensure timely completion of key milestones and deliverables
  • Partner with logistics providers to coordinate the timely delivery of clinical trial materials to sites and depots
  • Support the assessment, management, and release of temperature-related excursions affecting clinical sites and depots
  • Identify potential supply and distribution risks and work proactively with cross-functional teams and vendors to resolve issues
  • Provide ongoing operational support to ensure clinical supply activities remain aligned with study timelines and clinical needs

Experience Requirements:
MUST HAVES - QUALIFICATION SUMMARY
  • Minimum 3 years, Ideally 6+ years of relevant experience in clinical trial supply, clinical operations, or related
  • Experience supporting or managing global Phase 1-3 clinical trials
  • Experience managing or overseeing IRT systems and processes
  • Demonstrated experience with clinical trial supply forecasting, inventory management, logistics, and distribution
  • Experience working cross-functionally internal (Clinical, Quality, Regulatory) and with external vendors
  • Strong vendor and stakeholder management skills
  • Excellent organizational, communication, and problem-solving abilities
  • Ability to manage multiple priorities and operate effectively in a fast-paced clinical development environment

NICE-TO-HAVES
  1. Experience supporting or managing clinical trials in China
  2. Experience working with medical devices or device-related clinical trials

TRAVEL & LOCATION
REMOTE.
START & TERM
Immediate Start. 6 month initial contract with high likelihood to extend
Recruitment Transparency Notice

Eliassen Group values transparency in our recruitment practices. Please be advised that Eliassen Group utilizes artificial intelligence (AI) tools as part of its initial application screening and hiring process. You may receive email and SMS notifications from the Eliassen Virtual Recruiting Team (, ) inviting you to complete a brief voice screening as part of your application process. These tools assist our hiring teams in different ways, including but not limited to, assistance in reviewing application materials to help identify candidates whose qualifications most closely match the requirements of the position. All AI-assisted evaluations and responses are reviewed by human recruiters before any hiring decisions are made. The use of AI in our process is intended to support fairness, efficiency, and consistency, and Eliassen Group takes measures to prevent bias or discrimination in connection with its hiring practices. By proceeding, you acknowledge, agree, and consent to Eliassen Group's use of these tools, including AI tools, as part of the application and hiring process.
Skills, experience, and other compensable factors will be considered when determining pay rate. The pay range provided in this posting reflects a W2 hourly rate; other employment options may be available that may result in pay outside of the provided range.
W2 employees of Eliassen Group who are regularly scheduled to work 30 or more hours per week are eligible for the following benefits: medical (choice of 3 plans), dental, vision, pre-tax accounts, other voluntary benefits including life and disability insurance, 401(k) with match, and sick time if required by law in the worked-in state/locality.
If anyone reaches out to you about an open position connected with Eliassen Group, please ensure that you are working directly with us by confirming the following:
When you work with Eliassen Group, all email communication will come from an Eliassen.com address, never Gmail, Yahoo, etc.
Eliassen Group will never ask you for personal information (home address, bank account, or check routing number) until you have worked with someone clearly associated with Eliassen Group.
If you have any indication of fraudulent activity, please contact .
About Eliassen Group:
Eliassen Group is a strategic consulting firm that helps organizations reach further and achieve more through our technology, business advisory, and life sciences solutions. For nearly 40 years, we have combined exceptional people, deep domain expertise, and intelligent capabilities to expand our clients' capacity and accelerate meaningful outcomes. We are driven by a purpose to positively impact the lives of our employees, clients, consultants, and the communities we serve.
Eliassen is committed to building a diverse and inclusive team from a variety of backgrounds, perspectives, and skills. We are an Equal Opportunity and Affirmative Action Employer and all employment decisions are based on merit, performance, and business needs. Eliassen does not discriminate on the basis of race, color, gender identity or expression, sexual preference or orientation, sex (including pregnancy, childbirth, and related medical conditions), marital status, creed, religion, physical or mental disability, genetic information, military or veteran status, age, ancestry, national origin, citizenship status, prohibited criminal record inquiries of applicants and employees, or any other category protected by federal, state, or local laws.
Don't miss out on our referral program! If we hire a candidate that you refer us to then you can be eligible for a $1,000 referral check!
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About Eliassen Group

Sourced by ZipRecruiter

Eliassen Group provides strategic consulting and talent solutions to drive our clients' innovation and business results. Our purpose is to positively impact the lives of our employees, clients, consultants, and the communities in which we operate. Leveraging over 30 years of success, our expertise in talent solutions, life sciences consulting, Agile consulting, cloud services, risk management, business optimization, and managed services enables us to partner with our clients to execute their business strategy and scale effectively. Headquartered in Reading, MA, and with offices from coast to coast, Eliassen Group offers local community presence and deep networks, as well as national reach.

Industry

It services

Company size

5,001 - 10,000 Employees

Headquarters location

Reading, MA, US

Year founded

1989

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