Clinical Research Associate Role at IQVIA for BS Graduates | Apply Nowย
IQVIA, a global leader in clinical research and healthcare intelligence, is hiring a Clinical Research Associate (CRA), Sponsor Dedicated in Durham, North Carolina. This full-time, field-based role (Job ID: R1481725) offers the opportunity to make an impact by ensuring the highest standards in site monitoring, data accuracy, and regulatory compliance across clinical trials.
- Job Position: Clinical Research Associate
- Location:ย Durham, North Carolina (Field-based role)
- Job ID:ย R1481725
- JobType: Full-Time
About the Company
IQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence to the life sciences industry. With innovative solutions, IQVIA accelerates the development and commercialization of medical treatments, thereby improving patient outcomes and population health worldwide.
Clinical Research Associate Role – Job Description
As a Clinical Research Associate at IQVIA, you will perform site monitoring and management activities to ensure clinical trials comply with protocols, Good Clinical Practice (GCP), and regulatory requirements. You will collaborate with research sites, manage study documentation, and contribute to the successful execution of sponsor studies.
Key Responsibilities
- Conduct site monitoring visits (selection, initiation, monitoring, and close-out) per GCP and scope of work.
- Support subject recruitment plans and track progress to meet project needs.
- Provide protocol and study training to sites while maintaining regular communication.
- Ensure proper study conduct, escalate quality issues, and maintain compliance.
- Manage regulatory submissions, approvals, enrollment, CRF completion, and query resolution.
- Maintain site documents for the Trial Master File (TMF) and Investigator Site File (ISF).
- Prepare monitoring visit reports, follow-up letters, and required study documentation.
- Collaborate with study team members for project support.
- Oversee site financial management and invoice retrieval (where applicable).
Clinical Research Associate Role – Educational Qualification
Bachelorโs degree in a scientific discipline or healthcare field (preferred).
Experience and Skills
- Minimum 2 years of on-site monitoring experience required.
- Strong knowledge of GCP, ICH guidelines, and regulatory requirements.
- Excellent therapeutic and protocol knowledge.
- Proficiency in Microsoft Office Suite, laptop, and mobile tools.
- Strong organizational, problem-solving, and communication skills.
- Ability to manage time effectively and maintain professional relationships with coworkers, managers, and clients.
Keywords: Clinical Research Associate, Sponsor Dedicated, IQVIA, Durham, North Carolina, Scientific, Healthcare job, medical treatmentsย
