Clinical Research Associate - Sponsor Dedicated

IQVIA • Durham, NC

5d • $71,900 - $189,000 • Remote

About The Position

IQVIA is actively seeking experienced Clinical Research Associates II (CRA II) and Senior Clinical Research Associates (Sr. CRA) to support a range of clinical studies across multiple therapeutic areas nationwide. This is an exciting opportunity to join a global leader in clinical research and play a vital role in advancing innovative therapies that improve patient outcomes. In this role, you will be responsible for overseeing clinical trial sites to ensure studies are conducted in compliance with study protocols, regulatory requirements, Good Clinical Practice (GCP), International Council for Harmonization (ICH) guidelines, and sponsor expectations. Successful candidates will possess strong site management skills, a commitment to quality, and the ability to build productive relationships with investigators and site personnel.

Requirements

• Minimum of 2 years of independent on-site monitoring experience within the pharmaceutical, biotechnology, or CRO industry.
• Strong understanding of clinical research processes and regulatory requirements, including GCP and ICH guidelines.
• Knowledge of therapeutic areas and clinical trial protocols gained through industry experience and training.
• Proficiency with Microsoft Office applications, including Word, Excel, and PowerPoint, as well as mobile and electronic data capture technologies.
• Excellent verbal and written communication skills with the ability to effectively interact with investigators, site personnel, sponsors, and internal stakeholders.
• Strong organizational, problem-solving, and time management skills with the ability to manage multiple priorities in a fast-paced environment.
• Demonstrated ability to work independently while maintaining strong collaborative relationships with colleagues, clients, and study teams.

Nice To Haves

• Bachelor’s degree in Life Sciences, Healthcare, Nursing, or a related field preferred. Relevant education and professional experience may be considered in lieu of a degree.

Responsibilities

• Conduct all phases of site monitoring activities, including site selection, initiation, routine monitoring, and close-out visits.
• Evaluate site performance and ensure adherence to study protocols, GCP, ICH guidelines, and applicable regulatory requirements.
• Partner with investigative sites to develop, implement, and track patient recruitment and retention strategies that support enrollment goals.
• Deliver protocol-specific training and maintain ongoing communication with site staff to ensure alignment on study expectations and timelines.
• Identify, document, and escalate quality or compliance concerns while supporting timely resolution of issues.
• Monitor study progress by tracking regulatory submissions, approvals, enrollment metrics, CRF completion, and data query resolution.
• Ensure essential study documentation is complete, accurate, and maintained within the Trial Master File (TMF) and Investigator Site File (ISF).
• Prepare comprehensive monitoring reports, follow-up letters, and other required study documentation in accordance with company and sponsor standards.
• Collaborate cross-functionally with project teams to support study execution and achievement of project milestones.
• May participate in study start-up activities, site budget tracking, financial management, and site payment processes, depending on assignment.

Benefits

• 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.

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level