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.
Manage one or more clinical trials, including Investigational Device Exemption, post-approval, post-market surveillance, feasibility, and/or marketing studies
Develop clinical plan strategies and execute on clinical study protocols, timelines, and budget management
Collaborate with Clinical Operations Data Management on data collection, quality control and analysis of clinical trial patient data and radiographic results
Support Regulatory and Marketing functions in strategic clinical data needs
Communicate study results through annual reports, investigator meetings, and global clinical discussions; track study performance through metric-based results
Demonstrate leadership qualities and mentor members of the Clinical Operations team
Ensure compliance of clinical trials with federal and applicable regulatory agency requirements, Good Clinical Practices, and Standard Operating Procedures
Travel 50% to monitor a study.
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
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 jobs.iqvia.com.
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 firstname.lastname@example.org to arrange for such an accommodation.
Iqvia Holdings Inc