United States onlyJob Title: Clinical Research Coordinator - Abington, PA
Job Location: Abington, United States of America
Job Location Type: Office-based
Job Contract Type: Part time
Job Seniority Level:
Clinical Research Coordinator - Abington, PA
Work Set‑Up: On‑site
Scheduled Weekly Hours: 24 hours per week
About IQVIA
IQVIA is a global leader in advanced analytics, technology solutions, and clinical research services. We partner with the world’s leading pharmaceutical, biotechnology, and medical device companies to drive healthcare innovation. By combining deep scientific expertise with cutting‑edge technology, we deliver high‑quality data and insights that accelerate development and improve patient outcomes worldwide.
About the Role
IQVIA is seeking a Clinical Research Coordinator (CRC) to support clinical research studies under the supervision of a Principal Investigator. This role is essential to the successful execution of clinical trials and involves a mix of study coordination, hands‑on clinical procedures, and direct participant interaction. The ideal candidate is detail‑oriented, organized, and comfortable managing study visits while ensuring compliance, data integrity, and participant safety.
Key Responsibilities
- Perform clinical procedures such as ECGs, vital signs, and biological sample collection in accordance with study protocols.
- Coordinate daily clinical research activities while ensuring compliance with study requirements, Good Clinical Practice (GCP), and regulatory standards.
- Prepare, organize, and maintain study materials, equipment, and documentation to support study conduct.
- Recruit, screen, consent, and orient study participants, ensuring a positive and safe patient experience throughout the trial lifecycle.
- Conduct study visits, including informed consent, participant education, collection of medical history and medication information, and follow‑up activities.
- Accurately collect, document, and enter clinical data into case report forms (CRFs) and electronic data capture (EDC) systems.
- Collaborate with investigators, monitors, and study team members to resolve data queries and maintain high data quality.
- Serve as a patient advocate while maintaining a safe clinical environment in alignment with Health and Safety policies.
Qualifications
- Bachelor’s degree preferred, or an equivalent combination of education and relevant clinical research or healthcare experience.
- Minimum of 1+ year of clinical research experience, including hands‑on study coordination responsibilities.
- Experience coordinating clinical research studies and supporting protocol execution from participant recruitment through study visits.
- Comfortable independently conducting study visits, including informed consent, vital signs collection, medical history review, and documentation of medications.
- Working knowledge of clinical trials, GCP principles, and medical terminology.
- Experience with EDC systems, including accurate data entry and data query resolution.
- Familiarity with regulatory binders, study supply management, and study portals.
- Strong attention to detail with the ability to build effective working relationships across clinical and research teams.
Please note: This position is not eligible for sponsorship.
#ONSITE
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.This job is curated by Lifelancer.
Lifelancer is a talent-hiring platform in Life Sciences, Pharma and IT. The platform connects talent with opportunities in pharma, biotech, health sciences, healthtech and IT domains.
Please apply via Lifelancer platform to get connected to the application page and to find similar roles.
United Kingdom only