Job Description

Research Assistant

Work Setup: On-site
Scheduled Weekly Hours: 24

We are seeking a highly organized and detail‑driven Research Assistant to support clinical trial operations in accordance with regulatory, ethical, and organizational standards. This position plays an important role in ensuring data accuracy, participant safety, and smooth study execution. The ideal candidate brings strong critical thinking skills, adaptability in a fast‑paced environment, and exceptional communication and teamwork abilities.

Key Responsibilities

• Perform accurate EDC data entry, manage queries, and ensure timely resolution.
• Maintain and update the regulatory binder in compliance with documentation and audit standards.
• Coordinate and schedule subject visits, procedures, and follow-up activities
• Build effective working relationships with investigators, clinical staff, and study team members.
• Support subject screening, recruitment, and enrollment activities.
• Assist with patient/research participant scheduling and collection of medical history.
• Coordinate lab procedures and follow-up care in alignment with study protocols.
• Ensure strict adherence to IRB‑approved protocols, including assistance with informed consent processes.
• Uphold participant safety and report concerns promptly per SOPs and Sponsor requirements.
• Follow all company policies, SOPs, guidelines, and Good Clinical Practice (GCP) standards.

Qualifications

• Associate degree or equivalent combination of education and relevant experience.
• 1+ year of experience in a clinical research environment preferred.
• Strong working knowledge of clinical trials, GCP, and protocol‑specific procedures.
• Proficiency with EDC systems, data entry accuracy, and query management.
• Experience with visit scheduling, regulatory documentation, and binder maintenance.
• Excellent attention to detail, time management, and task prioritization.
• Strong communication, interpersonal, and relationship‑building skills.
• Any certifications or licenses required by the company, state, or regulatory agencies must be current.

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 $25.00-$39.00 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.