Clinical Research Associate, Sponsor Dedicated
Not Disclosed•Full-TimeOn-site
location_onOn-site
About the Team
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.
About the Role
This position is dedicated to performing monitoring and site management work to ensure that clinical sites are conducting studies and reporting data as required by the study protocol, applicable regulations, guidelines, and sponsor requirements. The role is designed for experienced candidates located near major hub airports in the Southeast, Northeast, Central, and West regions.
A significant component of this role involves 65-70% nationwide travel to perform site monitoring visits, including selection, initiation, monitoring, and close-out visits. You will work directly with sites to adapt, drive, and track subject recruitment plans, administer protocol training, and manage ongoing project expectations. The position requires evaluating the quality and integrity of site practices, managing study progress through regulatory submissions and data query resolution, and ensuring the proper maintenance of Trial Master Files (TMF) and Investigator's Site Files (ISF) in accordance with Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.
Eligibility and Location
To be eligible for this position, you must reside in the same country where the job is located. Candidates must be situated near major hub airports to facilitate the required travel schedule.
Equal Opportunity and Integrity
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.
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.
Work location
Work model: On-site
On-site
Key Responsibilities
- check_circleDrive and track subject recruitment plans to enhance predictability
- check_circleAdminister protocol training and establish regular communication with study sites
- check_circleCreate and maintain documentation including visit reports and follow-up letters
- check_circleCollaborate with study team members to support project execution
- check_circleManage study progress by tracking submissions, enrollment, and data query resolution
- check_circlePerform site monitoring visits including selection, initiation, monitoring, and close-out
- check_circleManage site financials and retrieve invoices according to clinical trial agreements
- check_circleSupport development of site-specific subject recruitment plans
- check_circleEvaluate site practices for quality, integrity, and regulatory adherence
- check_circleMaintain Trial Master Files and Investigator Site Files in compliance with GCP/ICH
Requirements
- verified2.5 years of clinical research coordination experience at site level
- verifiedNursing or University Degree (US Bachelor Level or equivalent) in one of the life sciences
- verifiedKnowledge of electronic data capture preferred
Nice to Have
Knowledge of electronic data capture
Similar Job Opportunities
Skills, education and keywords
Skills: Good Clinical Practice, Ich Guidelines, Electronic Data Capture, Clinical Research Coordination.
Education: Nursing or University Degree (US Bachelor Level or equivalent) in life sciences.
Frequently asked questions about Clinical Research Associate, Sponsor Dedicated at IQVIA
What does a Clinical Research Associate, Sponsor Dedicated at IQVIA do?expand_more
A Clinical Research Associate, Sponsor Dedicated at IQVIA is responsible for the following: Drive and track subject recruitment plans to enhance predictability; Administer protocol training and establish regular communication with study sites; Create and maintain documentation including visit reports and follow-up letters; and Collaborate with study team members to support project execution.
What are the requirements for this Clinical Research Associate, Sponsor Dedicated role?expand_more
IQVIA is looking for candidates who meet the following requirements: 2.5 years of clinical research coordination experience at site level; Nursing or University Degree (US Bachelor Level or equivalent) in one of the life sciences; and Knowledge of electronic data capture preferred.
Where is the Clinical Research Associate, Sponsor Dedicated role at IQVIA located?expand_more
Clinical Research Associate, Sponsor Dedicated at IQVIA is based in On-site. This is a on-site role.
Is this Clinical Research Associate, Sponsor Dedicated job remote, hybrid, or on-site?expand_more
IQVIA has listed this Clinical Research Associate, Sponsor Dedicated role as on-site.
How much experience is required for this Clinical Research Associate, Sponsor Dedicated role?expand_more
Clinical Research Associate, Sponsor Dedicated at IQVIA typically requires 2.5+ years of relevant experience at the mid level level.
What skills do you need for the Clinical Research Associate, Sponsor Dedicated role at IQVIA?expand_more
Key skills for Clinical Research Associate, Sponsor Dedicated at IQVIA include Good Clinical Practice; Ich Guidelines; Electronic Data Capture; and Clinical Research Coordination.
What education is required for Clinical Research Associate, Sponsor Dedicated at IQVIA?expand_more
Educational requirements for this role: Nursing or University Degree (US Bachelor Level or equivalent) in life sciences.
What category does the Clinical Research Associate, Sponsor Dedicated role belong to?expand_more
Clinical Research Associate, Sponsor Dedicated at IQVIA is part of the scientific & qa job category on Recrutus.
About IQVIA
IQVIA, headquartered in Durham, North Carolina, operates within the Hospitals and Health Care sector as a global provider of clinical research services, commercial insights, and healthcare intelligence. The organization serves the life sciences and healthcare industries by delivering actionable solutions powered by IQVIA Connected Intelligence, Healthcare-grade AI, advanced analytics, and extensive domain expertise. These capabilities are built upon high-quality health data and the latest technologies to support the development and commercialization of innovative medical treatments.
With a workforce of approximately 88,000 employees across more than 100 countries, IQVIA includes experts in healthcare, life sciences, data science, and operational excellence. The company supports a diverse range of stakeholders, including biotech firms, medical device manufacturers, pharmaceutical companies, medical researchers, government agencies, and payers. These partners utilize IQVIA's insights to gain a deeper understanding of diseases, human behaviors, and scientific progress.
A key focus of the organization is the protection of individual patient privacy. IQVIA employs various privacy-enhancing technologies and safeguards to secure personal data while enabling large-scale analysis of health information. This approach allows healthcare stakeholders to identify disease patterns and correlate them with precise treatment paths and therapies. The ultimate goal is to improve patient outcomes and population health worldwide through data-driven decision-making and advanced execution capabilities.
Browse more roles: All IQVIA jobs, scientific & qa jobs on Recrutus.