Clinical Research Coordinator - Somerset, NJ
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What you'll do
- Perform clinical procedures including ECGs, vital signs, and biological sample collection.
- Coordinate daily clinical research activities in compliance with study protocols and Good Clinical Practice (GCP) guidelines.
- Prepare 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.
- Accurately collect, document, and enter clinical data into case report forms (CRFs) and electronic data capture (EDC) systems.
- Collaborate closely with investigators, monitors, and study team members to resolve queries and maintain data quality.
- Serve as a patient advocate while maintaining a safe clinical environment in accordance with Health and Safety policies.
What they're looking for
- Minimum of 1+ year of experience in clinical research or a related healthcare setting.
- Working knowledge of clinical trials, GCP principles, and medical terminology.
- Experience conducting study visits, including patient education and chart review.
- Familiarity with maintaining regulatory binders, managing study supplies, and updating study portals.
- Strong attention to detail with the ability to build effective working relationships.
- Proficiency in EDC systems, accurate data entry, and query resolution.
Nice to have
- Bachelor’s degree preferred, or an equivalent combination of education and relevant experience.
- Exposure to cardiovascular studies and related clinical procedures is preferred.
Summarised by NextRaise from the employer’s description, which follows in full below.
Full description from employer
Clinical Research Coordinator - Somerset, NJ
Work Set-Up: On-site
Scheduled Weekly Hours: 40 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 forward. By combining deep scientific expertise with cutting-edge technology, we deliver high-quality data and insights that accelerate innovation and improve patient outcomes worldwide.
About the Role
We are seeking a Clinical Research Coordinator (CRC) to support clinical research studies under the supervision of a Principal Investigator. This role plays a critical part in the successful execution of clinical trials, combining hands-on clinical procedures, patient interaction, and study coordination to ensure compliance, data integrity, and participant safety.
Key Responsibilities
- Perform clinical procedures including ECGs, vital signs, and biological sample collection.
- Coordinate daily clinical research activities in compliance with study protocols and Good Clinical Practice (GCP) guidelines.
- Prepare 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.
- Accurately collect, document, and enter clinical data into case report forms (CRFs) and electronic data capture (EDC) systems.
- Collaborate closely with investigators, monitors, and study team members to resolve queries and maintain data quality.
- Serve as a patient advocate while maintaining a safe clinical environment in accordance with Health and Safety policies.
Qualifications
- Bachelor’s degree preferred, or an equivalent combination of education and relevant experience.
- Minimum of 1+ year of experience in clinical research or a related healthcare setting.
- Working knowledge of clinical trials, GCP principles, and medical terminology.
- Experience conducting study visits, including patient education and chart review.
- Exposure to cardiovascular studies and related clinical procedures is preferred.
- Familiarity with maintaining regulatory binders, managing study supplies, and updating study portals.
- Strong attention to detail with the ability to build effective working relationships.
- Proficiency in EDC systems, accurate data entry, and query resolution.
Please note: This position is not eligible for sponsorship.
#LI-CES #LI-DNP #LI-HCP #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.Company
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