Work Setup: On-site
Employment Type: Full-time
About IQVIA
IQVIA is a global leader in advanced analytics, technology solutions, and clinical research services, dedicated to driving healthcare forward. We partner with leading pharmaceutical, biotechnology, and medical device organizations to improve patient outcomes and accelerate innovation. By combining deep scientific expertise with advanced technology, we deliver high-quality data and insights that shape the future of clinical trials.
Position Overview
We are seeking a Clinical Research Coordinator (CRC) to support the successful execution of clinical trials under the supervision of a Principal Investigator. This role requires a detail-oriented, patient-focused professional who can manage clinical, operational, and data-related responsibilities while ensuring compliance with regulatory and protocol requirements.
Key Responsibilities
Perform clinical procedures including ECGs, vital signs, and biological sample collection in accordance with study protocols
Coordinate daily clinical trial activities while ensuring compliance with GCP, study protocols, and regulatory guidelines
Prepare study materials, maintain equipment, and support site readiness for study visits
Conduct patient recruitment and pre-screening activities, including chart review and phone screenings
Schedule and conduct patient study visits, ensuring protocol adherence and participant safety
Educate, consent, and orient study participants throughout the clinical trial process
Accurately collect, document, and enter clinical data into EDC systems and case report forms (CRFs)
Perform data review and resolve queries to maintain high-quality, audit-ready datasets
Collaborate with investigators, sponsors, and monitors, including support during monitoring visits and audits
Maintain a safe clinical environment and serve as a patient advocate in accordance with health and safety standards
Qualifications
Bachelor’s degree preferred or equivalent combination of education and relevant experience
Minimum of 1+ year of clinical research experience, including hands-on coordinating responsibilities
Demonstrated experience conducting study visits, patient recruitment, and pre-screening activities
Proficiency in clinical data entry, including use of EDC systems and query resolution
Working knowledge of clinical trial processes, GCP guidelines, and medical terminology
Strong attention to detail with the ability to manage multiple priorities in a fast-paced environment
Effective communication and interpersonal skills with the ability to collaborate cross-functionally
Additional Information
This position is not eligible for visa sponsorship
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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.