Senior Clinical Research Associate, Early Clinical Development

IQVIA LLC; Durham (NC); On-site; USD 87,200 - 169,300; Full time

Job summary

A leading clinical research organization in Durham, North Carolina, seeks a Senior Clinical Research Associate specialized in early clinical development. The candidate will monitor clinical sites to ensure compliance with protocols, manage subject recruitment strategies, and maintain communication with site personnel. A Bachelor’s degree in life sciences and at least 1.5 years of on-site monitoring experience are required. This role offers a competitive salary range of $87,200 - $169,300 annually, with potential bonuses and benefits.

Qualifications

• At least 1.5 years of on-site monitoring experience is required.
• Must possess a strong understanding of GCP, ICH guidelines, and regulatory requirements.

Responsibilities

• Conduct all types of site visits as per guidelines.
• Collaborate with site staff on recruitment strategies.
• Deliver training and manage communication with site personnel.
• Monitor study progress through regulatory submissions and enrollment.
• Document site management activities and outcomes.

Skills

On-site monitoring experience

Knowledge of Good Clinical Practice

Strong understanding of regulatory requirements

Site management

Collaboration skills

Education

Bachelor’s degree in life sciences or health-related field

Job description

Senior Clinical Research Associate, Early Clinical Development page is loaded## Senior Clinical Research Associate, Early Clinical Developmentlocations: Durham, North Carolina, United States of Americatime type: Full timeposted on: Posted Yesterdayjob requisition id: R1540075IQVIA Early Clinical Development is hiring for a Senior CRA 1. Ideal candidates will have Phase 1 experience across a variety of therapeutics. Seeking candidates located East Coast, US.**Job Overview** We are seeking a dedicated Clinical Research Associate (CRA) to join our team and play a key role in ensuring the successful execution of clinical trials. In this position, you will be responsible for monitoring and managing clinical sites to ensure compliance with study protocols, regulatory requirements, and sponsor expectations. Your work will directly contribute to the integrity and quality of clinical research data.**Key Responsibilities*** Conduct all types of site visits—selection, initiation, monitoring, and close-out in alignment with the contracted scope of work, Good Clinical Practice (GCP), and ICH guidelines.* Collaborate with site staff to implement and track subject recruitment strategies that align with project timelines and enrollment goals.* Deliver protocol and study-specific training to site personnel and maintain consistent communication to manage expectations and resolve issues.* Assess site performance and adherence to the protocol, escalating quality concerns as needed to ensure compliance and data integrity.* Monitor study progress by tracking regulatory submissions, subject enrollment, case report form (CRF) completion, and resolution of data queries.* Ensure that essential documents are collected and maintained in both the Trial Master File (TMF) and the Investigator Site File (ISF) in accordance with regulatory standards.* Document site management activities, visit outcomes, and follow-up actions through detailed reports and correspondence.* Work closely with cross-functional project teams to support study execution and ensure alignment with project goals.* Depending on the project, you may also support site-level recruitment planning and financial management, including invoice collection and budget tracking.**Qualifications*** Bachelor’s degree in life sciences or health-related field (or equivalent experience).* Requires at least 1.5 years of on-site monitoring experience.* Strong understanding of GCP, ICH guidelines, and regulatory requirements.* Ability to travel as required by the project.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 atIQVIA 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. We appreciate your honesty and professionalism.The potential base pay range for this role, when annualized, is $87,200.00 - $169,300.00. 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.IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.