Job Description
Quicksilver Scientific is a leading manufacturer of advanced nutritional systems with a focus on detoxification #liposomedeliverysystem. 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 in order 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. The Clinical Research Coordinator (CRC) is responsible for planning, designing, conducting, and management of clinical research projects as identified by the Organization. This role will work cross-functionally with other departments as it relates to the type of study being conducted, study goals, and outcomes.
On a daily basis, the CRC coordinates, facilitates, and manages the activities and subsequent data of both third-party clinical studies and internal clinical studies. The goal of these studies will support the development, application, and efficacy of Quicksilver products and protocols.
Responsibilities: Study Planning and Protocol Development - Participate in the development of research protocols with Clinical Research Organizations, ensuring they are comprehensive and adhere to ethical guidelines and regulatory requirements.
- Work cross departmentally to understand the needs of the business when identifying clinical projects.
Participant Recruitment and Management - Recruit and manage study participants, ensuring they meet the inclusion criteria and are fully informed about the study.
Data Collection and Management - Oversee data collection activities, ensuring data integrity and accuracy.
- Manage and organize data, including entering, storing, and retrieving information.
- Work cross-departmentally to create and build upon the appropriate systems to store and retrieve data.
Project Management - Manage specific clinical study and research-oriented projects including timelines, budgets, and resources to ensure projects are completed on time and within budget.
- Coordinate with various teams and stakeholders, including researchers, clinicians, industry partners, study participants, and internal teams.
Communication and Reporting - Maintain clear and effective communication with all stakeholders, including research teams, participants, and regulatory bodies.
- Prepare reports and presentations summarizing research findings.
Compliance and Ethics - Ensure that all research activities are conducted in accordance with ethical guidelines and regulatory requirements.
- Maintain accurate records and documentation of research activities.
Product Knowledge - Maintain a strong understanding of the products/technologies being studied.
Competencies: - High attention to detail and accuracy and strong organization and prioritization skills
- Strong Excel skills and ability to decipher, organize, and track data in a usable way
- Project management skills
- Proficiency in relevant software and tools.
- Excellent verbal and written communication skills
- Knowledge of research protocols, data collection methods, and regulatory requirements.
- Interpersonal communication skills and experience working in a team-oriented environment
- Self-starter with ability to take direction and work
Qualifications: BS degree in a relevant field (e.g., clinical research, science, healthcare) from an accredited program
At least 2 years of experience managing clinical research projects
Proficiency in MS Office suite
CCRP or CCRC preferred
Chemistry background preferred
Quicksilver Scientific 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
- Fitness Center membership
- Free use of products onsite and generous employee discount on all products
Compensation: $75,000 - $80,000 per year Location: Hybrid Remote
Physical Requirements: Ability to stand for long periods of time and lift up to 30 lbs.
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."
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Job Tags
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