Clinical Research Coordinator - Quicksilver Scientific, Inc

Quicksilver Scientific is a leading manufacturer of advanced nutritional systems with a focus on detoxification and liposomal delivery systems. As a pioneer in the natural health industry, our mission is to deliver on the promise of natural medicine to optimize quality of life.

We envision a company with an environment of collaboration & ideation that leads to innovations that break barriers in the quest for healthier lives. We value:

• Craftmanship & Integrity our products are crafted with premium ingredients and backed by science
• Agility, Audacity & Innovation we pivot and adapt to take chances and lead the way in natural health
• Continuous Improvement & Learning constant iteration and improvement is our hallmark
• Self-Awareness we strive for self-reflection and authenticity
• Mutual Respect, Openness & Exchange our teams work across functions with collaboration and reciprocity

Our growth is fueled by individuals who share our passion. Currently, we have an opening for a Clinical Research Coordinator in our Louisville, CO location responsible for coordinating, facilitating, and executing clinical trials and internal product and efficacy studies.

Core Responsibilities include:

In-house and third-party product clinical studies and/or trials:

• In conjunction with CEO, Research & Development, Education, New Product Development, and various other internal and external teams, champions both in-house and third-party study initiatives, supporting all phases from protocol and study design to execution of data.
• Depending on type of study, secures IRB (Independent Review Board).
• Maintains communication and acts as liaison between internal and external teams to include practitioners, study participants, education, marketing, R&D, and outside labs and organizations.
• Assists in the study feasibility assessment. Collects background information from academic papers, scientific literature, commercial publications, and professional contacts to assess the validity of the proposed clinical study.

• Collaborates with Finance to prepare a categorized budget and justification. Confirms accuracy and completeness of budgeted costs.

• Recruits and screens subjects, collects specimens, monitors experiments, analyzes data, and reports test results. Monitors research activity to ensure compliance with Standard Operating Procedures and Good Clinical Practices. Ensures participants have given informed consent and fully understand the implications of participating in research studies.
• Develops tools and materials necessary to run in-house studies from start to finish.

• In collaboration with various teams, formats study data to be used for marketing and education purposes.
• Supports R&D and Education teams with ingredient and related research.

Qualifications:

• 2+ years' experience in clinical research
• BS degree in Clinical Research or related field from an accredited program preferred
• Certified Clinical Research Coordinator (CCRC) or Certified Clinical Research Professional (CCRP) preferred
• Comprehensive knowledge of FDA regulations and ICH-Good Clinical Practices (GCP)
• Excellent research skills
• Ability to manage projects from start to finish
• Proficiency in MS Office suite
• Ability to multi-task, adhere to deadlines, and work both independently and cooperatively with interdisciplinary teams.
• Solid teamwork, organizational, interpersonal, analytical, and critical thinking skills, and attention to detail.
• Excellent verbal and written communication skills
• Experience with overseeing work at clinical sites and contract research organizations (pre-clinical and clinical)

Quicksilver offers a competitive benefits package including:

• Employer paid Medical, Dental and Life insurance, including Short-term and Long-term Disability
• 401(k) with company matching
• Four weeks Paid Time Off
• Paid company holidays
• Parental Leave
• Fitness Center membership
• Free use of products onsite and generous employee discount on all products

Compensation: $70,000 - $85,000 per year

Quicksilver Scientific is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, disability, age, or veteran status. This job posting is in compliance with the Colorado "Equal Pay for Equal Work Act."