Clinical Research Coordinator
- Employer
- University of Colorado System
- Location
- Colorado Springs, Colorado, United States
- Salary
- Competitive Salary
- Date posted
- Jan 3, 2025
View more categoriesView less categories
- Position Type
- Administrative, Academic Affairs, Research Administration
- Employment Type
- Full Time
Clinical Research Coordinator
Department of Human Physiology and Nutrition
Helen and Arthur E. Johnson Beth-El College of Nursing and Health Sciences
Elevate Your Career at UCCS: Innovate, Inspire, and Impact in the Rockies!
Who We Are
The University of Colorado Colorado Springs (UCCS) is a premier educational institution that prides itself on academic excellence, research, and community engagement and is actively seeking a Clinical Research Coordinator to join our team! UCCS offers a diverse and inclusive learning environment that fosters innovation, growth, and the holistic development of its students. The work location for this position is on-site . This positi on is Exempt fr om the Fair Labor Standards Act (FLSA) overtime provisions.
At the base of the Rocky Mountains, Colorado Springs is captivated by its stunning landscapes, making it a paradise for nature lovers. This city is more than its scenery—a mosaic of history, arts, and a vibrant tech scene. We invite you to join a community that cherishes outdoor adventure as much as forward-thinking growth, an exceptional setting for both career and lifestyle.
Salary Range : $ 49,462 - $ 63,822 annually . Co mpensation will be commensurate upon experience and qualifications.
Benefits at a Glance
At UCCS, our employees are our most valued asset. We're proud to offer:
- Generous Time Off : Enjoy 22 vacation days, 10 sick days, paid parental leave, 13 recognized holidays, and provisions for bereavement, jury duty, and FAMLI Leave.
- Robust Health Coverage : Our comprehensive medical plans cover preventative care at no cost, including a yearly mental health visit. Plus, benefit from affordable dental, vision plans, and competitive prescription drug prices.
- Financial & Retirement Benefits : Take advantage of our health savings, flexible spending accounts, and life and disability insurance. Plan for your future with our retirement options.
- Further Your Education : Avail nine waived credits per academic year for courses at any CU campus. We invest in your educational and professional growth.
- Wellness & More : From wellness programs aimed at achieving your best self to various additional benefits through CU Advantage, we prioritize well-being and holistic development.
- Want to know your total compensation? Use our calculator to get the complete picture!
The Department of Human Physiology and Nutrition is seeking a detail-oriented and highly motivated Clinical Research Coordinator to manage clinical trials and human physiological and nutritional studies. This position plays a crucial role in coordinating research activities to ensure the integrity and efficiency of study protocols while adhering to regulatory guidelines. The successful candidate will work closely with principal investigators, students, and participants to maintain high standards of compliance and data accuracy throughout the study process. Candidates are expected to play an educational role with students, adhering to the principles of Good Clinical Practice.
Essential Functions
The duties and responsibilities of the position include, but are not limited to:
- Assist faculty and students with the development and conduct of investigations in human physiology and nutrition.
- Coordinate and manage the day-to-day operations of human physiological and nutritional research studies, including laboratory space and equipment upkeep, participant recruitment, scheduling, staffing and data collection.
- Ensure studies are conducted in compliance with various regulations, including but not limited to Institutional Review Board (IRB), ClinicalTrials.gov, federal regulations, and institutional guidelines.
- Study participant recruitment and screening.
- Administer informed consent and ensure that participants
understand the study procedures.
- Maintain accurate and timely documentation, including case
report forms, study logs, and regulatory
documents. - Assist in the collection of physiological data (e.g., blood
draws, blood pressure, oxygen saturation,
exercise performance metrics). - Monitor participant safety and report adverse events or protocol deviations as necessary.
- Prepare study materials and equipment for data collection, such as ordering and preparing physiological measurement tools and ensuring calibration.
- Work with principal investigators, students, and research teams to develop and maintain research timelines and track study milestones.
- Coordinate sample collection, processing, and storage, ensuring proper labeling and documentation.
- Ensure accurate data entry and management of databases;
participate in data analysis as needed.
- Assist in drafting research reports and manuscripts for
publication.
- Provide support during audits or inspections by regulatory authorities.
Tentative Search Timeline
- Priority will be given to applications submitted by: February 2, 2025 .
- Potential interview dates: February 16, 2025 - March 8, 2025 .
- Potential start date: April 2025.
All employees of the University of Colorado Colorado Springs (UCCS) are required to complete training on policies and procedures administered by the Office of Institutional Equity (OIE), under the supervision of the Associate Vice Chancellor of Institutional Equity/Title IX Coordinator. Required training includes: understanding and reporting conduct prohibited by the sexual misconduct, protected class nondiscrimination, and conflicts of interest in cases of amorous relationships policies, related retaliation, and compliance with accommodations regarding disability, pregnancy or related conditions, and religion. All employees are also designated as “responsible employees” and are required to report conduct prohibited under these policies, and student disclosures of pregnancy or related conditions directly to the OIE and to provide OIE’s contact information to any student disclosing pregnancy or related conditions. More information is available at: Policies and Resolution Procedures | Office of Institutional Equity (uccs.edu) .
Note: This job description outlines this role's general responsibilities, qualifications, and physical requirements at UCCS. It is not an exhaustive list of all required duties, responsibilities, and qualifications. The university reserves the right to modify, add, or remove duties and responsibilities as needed to meet the university's needs.
Qualifications :
- Education: A Bachelor's degree (BS) in Human Physiology, Biology, Health Sciences, Nursing or a related field is required.
- Experience:
- Familiarity with clinical research regulations, including IRB
processes and Good Clinical Practice (GCP) is required.
- Previous experience in physiological measurements (e.g., ECG,
metabolic carts, etc.) is required.
- Basic life support (BLS) certification or similar clinical certifications is required.
- Experience conducting clinical trials is preferred.
- Familiarity with clinical research regulations, including IRB
processes and Good Clinical Practice (GCP) is required.
In accordance with the Equal Pay for Equal Work Act, UCCS does not discriminate based on sex in our employment or compensation practices.
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