Clinical Research Coordinator - Boulder, CO

IQVIA Argentina; Boulder (CO); On-site; USD 48,000 - 58,000; Full time

Job summary

IQVIA in Boulder, CO is seeking a Clinical Research Coordinator to assist with hands-on clinical procedures under a principal investigator. This on-site position is 24 hours per week and focuses on data collection, patient safety, and adherence to GCP.

Key tasks include ECG, sample collection, vital signs, coordinating studies, preparing materials, recruiting and orienting patients, and entering data into CRFs while ensuring data quality and regulatory compliance.

Qualifications

• Bachelor’s degree or equivalent education/experience.
• Minimum 1+ year of relevant clinical research experience.
• Knowledge of trials, GCP, and medical terminology.
• Proficiency with EDC systems and data queries.

Responsibilities

• Perform ECG, sample collection, and vital signs.
• Coordinate studies and ensure protocol/GCP compliance.
• Prepare materials, set up equipment, plan logistics.
• Recruit, screen, and orient patients safely.
• Record data in CRFs accurately.
• Collaborate with investigators and monitors on data quality.

Skills

Clinical research

GCP principles

Attention to detail

Communication

Data entry accuracy

Patient safety

Education

Bachelor's degree or equivalent education/experience

Tools

EDC systems

Job description

Clinical Research Coordinator - Boulder, CO

Work Set-Up: On-site
Schedule Weekly Hours: 24 hours/week

About IQVIA

IQVIA is a global leader in advanced analytics, technology solutions, and clinical research services, dedicated to driving healthcare forward. We partner with the world’s leading pharmaceutical, biotechnology, and medical device companies to improve patient outcomes and accelerate innovation. Our team combines deep scientific expertise with cutting-edge technology to deliver high-quality data and insights that shape the future of clinical trials.

About the Role

We are seeking a Clinical Research Coordinator (CRC) to join our team and support clinical research studies under the supervision of a principal investigator. This role involves hands-on clinical procedures, community outreach, and ensuring the highest standards of care and compliance.

Key Responsibilities

• Perform a variety of clinical procedures, including ECG, sample collection, and vital signs.
• Coordinate clinical research studies and maintain compliance with protocols and Good Clinical Practice (GCP) guidelines.
• Support study conducts by preparing study materials, setting up equipment, and planning logistical activities.
• Recruit, screen, and orient patients, ensuring their safety and well-being throughout the study.
• Collect and accurately record clinical data in case report forms (CRFs).
• Collaborate with investigators and monitors, addressing queries and ensuring data quality.
• Act as a patient advocate and maintain a safe environment in accordance with Health and Safety policies.

Qualifications

• Bachelor’s degree preferred or equivalent combination of education and relevant experience.
• Minimum 1+ years of relevant work experience in clinical research.
• Working knowledge of clinical trials, GCP principles, and medical terminology.
• Strong attention to detail and ability to establish effective working relationships.
• Proficiency with EDC systems, data entry accuracy, and query management.

Please note: This position is not eligible for sponsorship.

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com

IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

The potential base pay range for this role is $35.00-$42.00 per hour. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.