Clinical Research Coordinator

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.

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.

• 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

• 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
• 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

• 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

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

• 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

• 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

• 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
• Comfortable handling and processing human biologic specimens

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.

• 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…