Clinical Research Coordinator

Quicksilver Scientific, Inc; Louisville (CO); On-site; USD 60,000 - 80,000; Full time

Benefits offered by this job

Competitive salary

Annual bonus opportunity

Medical, dental, and vision insurance

Company-paid life insurance

401(k) with company match

Paid time off and holidays

Product discounts

Summer Fridays

Collaborative culture

Job summary

Quicksilver Scientific, Inc is seeking a Clinical Research Coordinator to lead planning, coordination, and execution of clinical studies supporting product innovation and regulatory compliance. You will collaborate with CROs, investigators, and labs to ensure quality deliverables and adherence to timelines.

The role requires a bachelor’s degree in a related field, at least one year of coordination experience, strong Excel skills, and the ability to manage multiple projects in a fast-paced

Qualifications

• Bachelor's degree in a related scientific field is required.
• Minimum one year of clinical research or study coordination experience.
• Experience managing projects with multiple stakeholders.
• Strong Microsoft Office skills, especially Excel.
• AI acumen and ability to leverage emerging technologies.

Responsibilities

• Coordinate planning, coordination, and execution of clinical research studies.
• Collaborate with cross-functional teams and external partners to ensure on-time, on-budget studies.
• Develop project timelines, budgets, and study documentation.
• Coordinate participant recruitment, screening, enrollment, and follow-up.
• Oversee data collection, validation, and organization with GCP compliance.
• Prepare study updates, presentations, and summaries for stakeholders.

Skills

Analytical skills

Organizational skills

Communication skills

Project management

AI acumen

Education

Bachelor's degree in Clinical Research, Biological Sciences, Healthcare, Public Health, Nursing, or related field

Tools

Excel

Microsoft Office

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.