IQVIA™ is the leading human data science company focused on helping healthcare clients find unparalleled insights and better solutions for patients.
Formed through the merger of IMS Health and Quintiles, IQVIA offers a broad range of solutions that harness the power of healthcare data, domain expertise, transformative technology, and advanced analytics to drive healthcare forward.
Evidence Driven Design services are a component of IQVIA CoreTM enabled Clinical Development solutions. These services integrate drug development and trial design expertise with real world data, transformative technologies, methods, and work models.
The Design Analyst defines data needs, conducts design analytics, and develops and delivers 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 Lead.
Support Design Analytics Leads in the conduct and delivery of Protocol Assessments as part of new opportunity development and on-going project delivery.
Responsibilities include working with sales, Medical and therapeutic strategy leads, and global feasibility leads and other stakeholders to understand key challenges within a protocol design, identifying and executing standard and custom analytics to pressure test protocols, and interpreting and summarizing the findings from those analytics into meaningful insights.
Ensure quality and timely project deliverables
Partner cross functionally to present protocol assessment findings and to determine collaboratively how to apply the results
Ensure all relevant data is leveraged for and included in client 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
Input into, review, and production of proposal text
Contribute to training and support of new team members
Participate in the continuous improvement of departmental processes and procedures
May participate in functional area initiatives, special project assignments and act as departmental cross functional liaison.
Maintain proficiency of skills and knowledge and remain current with industry trends based on current literature
REQUIRED KNOWLEDGE, SKILLS AND ABILITIES
Good knowledge of medical terminology, GCP, FDA regulations, and Drug Development process,
understanding of clinical research
Tolerance for technological challenges
Proven experience of managing raw data, through to aggregated information, to drive knowledgeable outcomes
Demonstrated entrepreneurial spirit and role / task versatility
comfort with ambiguity and novel situations
Capacity and disposition for collaboration across disciplines
Self-starter, highly motivated, quick learner
Knowledge of decision analysis techniques, database analysis methods, basic statistical analysis and reporting, and technical writing
Strong computer literacy, including database mining and Microsoft Office applications
Ability to establish and maintain effective working relationships with coworkers, managers and customers
Excellent communication (verbal and written), organizational and interpersonal skills
Ability to work independently, manage time and multiple tasks, and effectively prioritize tasks
MINIMUM 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 3+ years’ experience in, clinical planning, and / or clinical trial operations preferred
Demonstrated aptitude with novel technologies and applied data analytics