PURPOSEThe Design Analytics Lead owns the development and delivery of data-informed protocol assessments. This includes conducting design analytics, partnering with clinical trial experts to develop and deliver insights based on those analytics, drafting reports and structured outputs to support protocol assessments and trial design decision-making.
This an individual contributor role that reports to a regionally-based Design Analytics Line Management.RESPONSIBILITIES
Lead and manage the delivery of assigned protocol assessments as part of new opportunity development and on-going project delivery.
Responsibilities include collaborating cross-functionally with medical and therapeutic strategy leads and other stakeholders to understand key challenges within a protocol design, identifying and executing standard and custom analytics to pressure test protocols, interpreting and summarizing the findings from those analytics into meaningful insights;
leading internal stakeholder review of the design analytics results; finalizing the results report; and presenting insights to internal stakeholders and clients.
Ensure quality and timely project deliverables.
Make recommendations and suggestions to the team regarding data utilization and process implementation
Coordinate the collection and delivery of appropriate data and analytics from broad range of sources to address trial design related questions
Reconcile and interpret cross-functional data
Function as a subject matter expert for data sources and tools utilized within the protocol assessment process
Participate in Business Development, Marketing and Sales activities. Deliver expert presentations on topics of interest to potential customers.
Provide input into, review, and production of proposal text and bid defense presentations
Participate in the continuous improvement of departmental processes and proceduresREQUIRED KNOWLEDGE, SKILLS AND ABILITIES
Good knowledge of medical terminology, GCP, FDA regulations, and Drug Development process
Strong demonstrated technical understanding - scientific, operational and commercial
Knowledge of decision analysis techniques, database analysis methods, basic statistical analysis and reporting, and technical writing
Good influencing and negotiation skills
Excellent customer service skills
Ability to work independently, manage time and multiple tasks, effectively prioritize tasks, delegate and escalate as appropriateMINIMUM REQUIRED EDUCATION AND EXPERIENCE
Bachelor's degree or educational equivalent in medical, science, or informatics related field or equivalent experience
Clinical research drug development experience - 8+ years of experience in clinical design, planning, and / or clinical trial operations preferred
Demonstrated aptitude with novel technologies and applied data analyticsAt 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 70,000+ employees around the world who apply their insight, curiosity and intellectual courage every step of the way.
Learn more at 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.EEO Minorities / Females / Protected Veterans / Disabled