BASIC FUNCTIONS : To conduct clinical trial feasibility assessments based on Request for Proposals (RFPs).To conduct ad-hoc research as requested by IQVIA Biotech Sr.
Management. ESSENTIAL JOB FUNCTIONS, DUTIES AND RESPONSIBILITIES : + Primarily leads the data-driven feasibility assessment of pre-award studies during the proposals process, and at times, supports new feasibility assessments for post-award studies.
Supports the proposal generation, site identification, bid defenses, and other internal or client-facing meetings.+ Plans, organizes, and conducts research assignments to increase scientific knowledge on medical-related topics.
It is expected that these research efforts contribute positively toward fostering internal knowledge regarding a sponsor's investigational product, as well as externally validating IQVIA Biotech's capabilities and strategies to the sponsor.
Researches pertinent scientific / clinical information that may include, but is not limited to : disease background (etiology, epidemiology, statistical information, symptoms, and methods of diagnosis), current standards of care (treatments methods), how the sponsor-proposed intervention fits into the current treatment landscape, and information regarding competing therapeutics in clinical development.
This information is augmented with a critical evaluation of the clinical trial protocol and supporting documents, to proactively identify study strengths and potential pitfalls.
Additionally, findings are communicated in strategy meetings with management and are often included in bid defense presentations.
Thorough knowledge of the feasibility and proposal processes. Ability to maintain long-range projects while managing daily details with a high degree of accuracy.
MINIMUM RECRUITMENT STANDARDS : + Bachelor's degree in a scientific field (advanced scientific / clinical degree, such as PhD, or PharmD, preferred) and 1 - 2 years of direct experience in scientific report or manuscript writing, which includes one year of relevant / related experience within a CRO setting, as a strategic feasibility analyst, or in an operational function.
Prior experience in publishing peer-reviewed publications and giving scientific / clinical research presentations.+ Ability to work independently, prioritize and work in a team environment is essential.
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 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.
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