at IQVIA
Location
Philadelphia, PA
Compensation
$73k–$87k USD
Type
part time
Posted
Today
Remote
Yes
Market range · company + function + seniority
p25 · target · p75 · n=72
Posted $87k · in the market band
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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 cutting-edge 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 research studies under the direction of a Principal Investigator. This is a hands-on role requiring clinical, operational, and patient-facing expertise to ensure studies are conducted safely, efficiently, and in compliance with regulatory standards.
Key Responsibilities
Perform clinical procedures such as ECGs, vital signs, and biological sample collection in accordance with study protocols
Coordinate day-to-day clinical trial activities while ensuring compliance with GCP, protocol, and regulatory requirements
Prepare study materials, organize equipment, and support overall site readiness
Conduct patient recruitment activities, including chart review, phone screening, and scheduling study visits
Perform and manage patient study visits in accordance with protocol requirements
Educate and orient participants, ensuring a high standard of patient care and safety
Accurately collect, document, and enter data into EDC systems and case report forms (CRFs)
Resolve data queries in a timely manner and maintain high data quality standards
Collaborate with investigators, sponsors, and monitors during site visits and audits
Serve as a patient advocate and maintain a safe, compliant clinical environment
Qualifications
Bachelor’s degree preferred, or an equivalent combination of education and relevant experience
Minimum of 1+ years of clinical research experience in a coordinator or similar role
Working knowledge of clinical trial processes, GCP guidelines, and medical terminology
Proven ability to conduct patient study visits in accordance with protocol requirements
Experience in patient recruitment, including chart review and phone screenings
Proficiency with EDC systems, including accurate data entry and query resolution
Strong attention to detail, organizational skills, and ability to manage multiple priorities
Effective communication skills and ability to build collaborative working relationships
Cardiovascular research experience preferred
Why Join IQVIA?
Be part of a global organization at the forefront of clinical innovation
Collaborate with industry-leading experts and researchers
Contribute to advancing treatments that improve patient lives
Note: This position is not eligible for visa sponsorship
#LI-CES and #LI-DNP #LI-HCP #remote
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.Open postings ranked by description similarity — useful if this role isn't quite right.