Job details
Job type full-time
Full job description
Iqvia biotech provides flexible, tailored, integrated clinical and commercial solutions designed to help smaller biotech companies move forward in their effort to get treatments to patients – from defining the plan for their asset, to trial design and implementation, through launch and commercialization – all while delivering compelling results to investors, stakeholders and regulatory authorities with confidence.
We offer this type of flexibility with our employees as wellCome join us and be part of the iqvia biotech family.
Responsibilities include:
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
Qualifications:
5+ years of experience as a clinical trial management/lead, 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
#li-rw1
#li-remote
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 worldThe advanced analytics, technology solutions and contract research services we provide to the life sciences industry are made possible by our 70,000+ employees around the world who apply their insight, curiosity and intellectual courage every step of the wayLearn more at jobs.iqvia.com.
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, incProvides reasonable accommodations for applicants with disabilitiesApplicants 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 workday_recruiting@iqvia.com to arrange for such an accommodation.
