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Role Overview: As a Clinical Research Associate, you’ll be at the forefront of ensuring our study sites operate smoothly and efficiently. Your work will be pivotal in advancing groundbreaking research.

Key Responsibilities:

• Site Visits: Conduct selection, initiation, monitoring, and close-out visits, ensuring compliance with Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.

• Recruitment Drive: Collaborate with sites to develop and track recruitment plans, ensuring project needs are met.

• Training & Communication: Provide protocol training and maintain regular communication with sites to manage expectations and address issues.

• Quality Assurance: Evaluate site practices for protocol adherence and escalate quality issues as needed.

• Study Progress: Track regulatory submissions, recruitment, enrollment, and data management to ensure smooth study progress.

• Documentation: Maintain essential documents in the Trial Master File (TMF) and Investigator’s Site File (ISF) as per regulatory requirements.

• Mentorship: Mentor clinical staff through co-monitoring and training visits.

• Collaboration: Work closely with study team members to support project execution.

• Financial Management: Manage site finances and retrieve invoices as per local requirements.

Qualifications:

• Education: BS Degree in a scientific discipline or healthcare preferred.

• Experience: Minimum 1 year of on-site monitoring experience in oncology; 2 years preferred.

• Knowledge: Strong understanding of GCP and ICH guidelines, with expertise in oncology protocols.

• Skills: Proficiency in Microsoft Office, excellent communication skills, and strong organizational and problem-solving abilities.

• Attributes: Effective time and financial management, and the ability to build strong working relationships.

Why Join Us? Be part of a team that’s driving innovation in clinical research. Your contributions will help shape the future of healthcare. Apply now and embark on a rewarding career journey with us!

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

We are committed to providing equal employment opportunities for all, including veterans and candidates with disabilities. https://jobs.iqvia.com/eoe

IQVIA’s ability to operate and provide certain services to customers and partners necessitates IQVIA and its employees meet specific requirements regarding COVID-19 vaccination status. https://jobs.iqvia.com/covid-19-vaccine-status

The potential base pay range for this role, when annualized, is $87,200.00 - $189,000.00. 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 world leader in using data, technology, advanced analytics, and expertise to help customers drive healthcare – and human health – forward. Together with the companies we serve, we are enabling a more modern, more effective and more efficient healthcare system, and creating breakthrough solutions that transform business and patient outcomes.

To get there, it takes diverse skills and a curiosity to explore new possibilities. No matter your role, everyone at IQVIA, including our colleagues at Q² Solutions, contributes to our shared goal of improving human health. Thank you for your interest in growing your career with us.

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