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IQVIA Clinical Regulatory Specialist, Device (Contract, Home-Based) - RSS in Indianapolis, Indiana

Unleash Your Potential

It takes curiosity and intellectual courage to accomplish great things. It takes brave minds to bring powerful ideas to reality and transform healthcare.

We are a diverse, global team that shares a passion for collaboration and solving complex problems. Together, we help customers drive healthcare forward.

Join IQVIA and see where your skills can take you.

Responsibilities include:

  • Prepare and analyze clinical data, journal articles and scientific presentations, as applicable, to support regulatory submissions

  • Manage one or more post-approval, post-market surveillance clinical trials

  • Develop clinical plan strategies and assist in the execution of clinical study protocols, timelines, and budget management

  • Collaborate with Regulatory and Quality Affairs on clinical data analysis and post-market surveillance

  • Support Marketing functions in strategic clinical data needs

  • Ensure compliance of clinical trials with federal and applicable regulatory agency requirements, Good Clinical Practices, and Standard Operating Procedures


  • 5+ years of experience as a Clinical Research Associate, Clinical Project Manager or equivalent external position

  • Experience in the medical device field preferred; experience in the pharmaceutical industry considered

  • Demonstrated clinical regulatory experience including knowledge of applicable US and OUS regulations and clinical data requirements, and preparation of clinical sections of regulatory submissions for FDA and international agencies.

  • Applied knowledge of project management tools

  • Demonstrated interpersonal, written and oral communication skills

  • Demonstrated organization and planning skills

  • Demonstrated success in a team-based environment preferred

  • Demonstrated knowledge and application of personal computer systems and desktop applications



At IQVIA, we believe in pushing the boundaries of human science and data science to make the biggest impact possible – to help our customers create a healthier world. The advanced analytics, technology solutions and contract research services we provide to the life sciences industry are made possible by our 67,000+ employees around the world who apply their insight, curiosity and intellectual courage every step of the way. Learn more at .

IQVIA is an EEO Employer - Minorities/Females/Protected Veterans/Disabled

IQVIA, Inc. provides reasonable accommodations for applicants with disabilities. Applicants who require reasonable accommodation to submit an application for employment or otherwise participate in the application process should contact IQVIA’s Talent Acquisition team at to arrange for such an accommodation.

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.