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Clinical Research Startup Jobs in Colorado (NOW HIRING)

The US Oncology Network

Study Coordinator

Denver, CO · On-site

$60K - $75K/yr

... within the research department * Planning and tracking of all assigned clinical activity in the lifecycle phases of the startup, interim and close out. * Updates clinical teams on protocol ...

The US Oncology Network

Study Coordinator

Denver, CO

$60K - $75K/yr

... within the research department * Planning and tracking of all assigned clinical activity in the lifecycle phases of the startup, interim and close out. * Updates clinical teams on protocol ...

Syneos Health, Inc.

Medical Science Liaison

Denver, CO · On-site

$190 - $210/hr

Simultaneously, you will partner with clinical research stakeholders to support the successful ... support effective study startup, protocol understanding, and trial execution. * Execute ...

Syneos Health

Medical Science Liaison

Denver, CO · On-site

$190 - $210/hr

Simultaneously, you will partner with clinical research stakeholders to support the successful ... support effective study startup, protocol understanding, and trial execution. * Execute ...

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All JobsClinical Research Startup JobsClinical Research Startup Jobs in Colorado

Clinical Research Startup information

See Colorado salary details

$51.5K

$112.9K

$198.7K

How much do clinical research startup jobs pay per year?

As of Aug 26, 2026, the average yearly pay for clinical research startup in Colorado is $112,866.00, according to ZipRecruiter salary data. Most workers in this role earn between $85,200.00 and $128,800.00 per year, depending on experience, location, and employer.

What is a clinical research startup?

A Clinical Research Startup job involves managing the initial phases of clinical trials, ensuring all regulatory, budgetary, and contractual requirements are met before a study begins. Professionals in this role coordinate with sponsors, sites, and regulatory bodies to obtain necessary approvals and facilitate site activation. Key responsibilities include submitting essential documents, negotiating contracts, and ensuring compliance with ethical guidelines. This position is crucial in ensuring trials start efficiently and adhere to regulatory standards.

What are the key skills and qualifications needed to thrive in the clinical research startup position?

To thrive in Clinical Research Startup roles, you need strong project management skills, knowledge of clinical trial regulations, and a background in life sciences or healthcare. Familiarity with regulatory submission systems (such as IRB portals), electronic trial master file (eTMF) systems, and GCP (Good Clinical Practice) certification are often required. Attention to detail, excellent organizational skills, and effective communication are valuable soft skills for success in this field. These skills ensure smooth trial startup, regulatory compliance, and successful collaboration across study teams and sponsors.

What are the common challenges faced in clinical research startup roles?

Professionals working in Clinical Research Startup frequently encounter challenges like tight start-up timelines, managing multiple site and regulatory submissions, and navigating evolving regulatory requirements. You’ll often need to coordinate between investigators, clinical sites, sponsors, and regulatory bodies to ensure all documentation is complete and compliant. Effective multitasking and strong communication are crucial when addressing unforeseen delays or changes in protocol. Mastering these challenges not only enhances study success but also provides valuable experience for growing into senior or project management roles within clinical research.

What are the most commonly searched types of Clinical Research Startup jobs in Colorado?

The most popular types of Clinical Research Startup jobs in Colorado are:

What are popular job titles related to Clinical Research Startup jobs in Colorado?

For Clinical Research Startup jobs in Colorado, the most frequently searched job titles are:

What job categories do people searching Clinical Research Startup jobs in Colorado look for?

The top searched job categories for Clinical Research Startup jobs in Colorado are:

What cities in Colorado are hiring for Clinical Research Startup jobs?

Cities in Colorado with the most Clinical Research Startup job openings:

Clinical Research Startup jobs near you
Infographic showing various Clinical Research Startup job openings in Colorado as of August 2026, with employment types broken down into 3% As Needed, 73% Full Time, 16% Part Time, 1% Temporary, and 7% Contract. Highlights an 94% Physical, 1% Hybrid, and 5% Remote job distribution, with an average salary of $112,866 per year, or $54.3 per hour.

Clinical Research Coordinator

Quicksilver Scientific, Inc

Louisville, CO • On-site

$72K - $88K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 29 days ago

Job description

Help advance the science behind innovative wellness solutions.
At Quicksilver Scientific, we're passionate about transforming health through cutting-edge nutritional science. Our research-backed products and advanced delivery technologies are changing the way practitioners and consumers approach wellness. As we continue to expand our scientific research initiatives, we're looking for a Clinical Research Coordinator who is organized, analytical, and excited to play a key role in bringing high-quality clinical research to life. If you thrive in a fast-paced environment, enjoy managing complex projects, and want your work to directly contribute to innovative health solutions, we'd love to hear from you.
What You'll Do
As our Clinical Research Coordinator, you'll oversee the planning, coordination, and execution of clinical research studies that support product innovation, scientific validation, and educational initiatives. You'll collaborate with cross-functional teams and external research partners to ensure studies are completed on time, within budget, and in compliance with regulatory standards.
Your Impact
Lead Clinical Research Studies
  • Coordinate clinical research studies from startup through closeout
  • Assist with study design, protocol development, and implementation
  • Partner with Clinical Research Organizations (CROs), investigators, laboratories, and academic institutions
  • Monitor study progress and proactively resolve issues that impact timelines or quality

Drive Project Success
  • Develop project timelines, budgets, and study documentation
  • Coordinate activities across multiple departments and external partners
  • Track milestones and communicate progress to stakeholders
  • Manage multiple research projects while balancing competing priorities

Support Study Participants
  • Coordinate participant recruitment, screening, enrollment, scheduling, and follow-up
  • Ensure informed consent is completed according to ethical and regulatory standards
  • Maintain participant confidentiality and accurate study records

Manage Clinical Data
  • Oversee data collection, validation, and organization
  • Ensure data accuracy, integrity, and compliance with Good Clinical Practice (GCP)
  • Perform quality reviews and assist with data analysis
  • Maintain organized, audit-ready study documentation

Ensure Regulatory Compliance
  • Maintain compliance with GCP, IRB requirements, and applicable regulations
  • Support protocol amendments, adverse event reporting, and regulatory submissions
  • Prepare for internal and external audits

Communicate Research Findings
  • Serve as the primary contact for assigned clinical studies
  • Prepare study updates, presentations, and research summaries
  • Present project progress to leadership and cross-functional teams

What You'll Bring
Required Qualifications
  • Bachelor's degree in Clinical Research, Biological Sciences, Healthcare, Public Health, Nursing, or a related scientific field
  • Minimum one year of clinical research or clinical study coordination experience
  • Experience managing projects involving multiple stakeholders
  • Strong Microsoft Office skills, especially Excel
  • AI acumen and the ability to leverage emerging technologies to improve efficiency
  • Excellent organizational, analytical, and communication skills

Preferred Qualifications
  • Two or more years of clinical research experience
  • CCRC or CCRP certification
  • Experience working with CROs, IRBs, or regulated clinical environments
  • Experience with Electronic Data Capture (EDC) or Clinical Trial Management Systems (CTMS)
  • Experience in the nutraceutical, supplement, pharmaceutical, or healthcare industry
  • Experience working in a growing, entrepreneurial company
  • Certified phlebotomist
  • Comfortable handling and processing human biologic specimens

Why You'll Love Working Here
At Quicksilver Scientific, science, innovation, and collaboration drive everything we do. We believe our employees are our greatest asset, and we invest in their success through meaningful work, outstanding benefits, and opportunities for growth.
Our Benefits Include
  • Competitive salary plus annual bonus opportunity
  • Comprehensive medical, dental, and vision insurance
  • Company-paid life insurance and disability coverage
  • 401(k) with company match
  • Generous Paid Time Off and paid company holidays
  • Generous employee product discounts
  • Summer Friday schedule (4½-day workweeks during the summer)
  • Collaborative, mission-driven culture focused on innovation and wellness

Work Schedule
Monday-Friday 8:30 AM-5:00 PM (Hours may vary based on business needs)
Why This Role Matters
Clinical research is at the heart of Quicksilver Scientific's commitment to delivering products backed by science. In this role, you'll help generate the evidence that supports product innovation, practitioner education, and consumer confidence. Your work will directly influence the future of wellness by ensuring every study is conducted with excellence, integrity, and scientific rigor. If you're passionate about clinical research and excited to make a meaningful impact in a growing, science-driven organization, we'd love to hear from you.
Join us in advancing the science of wellness.

Apply