Job details
Job Type
Full-time

Full Job Description

Job Overview
Responsible for providing input into the generation of the study strategies and collaborating with other involved IQVIA teams. Perform, manage and co-ordinate activities for assigned opportunities/ projects. Perform data mining and analysis, formulate recommendations and present to internal and potentially external stakeholders.

Essential Functions
  • Accountable for the generation, analysis and interpretation of study related information to produce and recommend prioritized site / investigator lists during pipeline planning, early engagement, the pre-award bidding process and post award, ensuring lists are tailored and accurate in order to set IQVIA operational teams up for successful delivery of each study
  • Participates in the analytics planning and site strategy review sessions with internal stakeholders to first align on requirement for data analytics that will inform decisions on the development of the strategy, and then ensure the final site list deliverable meets expectations
  • Leverages multiple and relevant data sources to develop each site/investigator strategy and list utilizing in-depth understanding of the data and methodologies used to develop tiered site / investigator lists
  • Collaborates with the ACOE Country Data Analysts, pre-award strategy teams and post-award project teams to coordinate and manage activities related to the generation of country-specific patient density data in support of Site ID and Enrollment Planning & Trends activities
  • Supports achievement of targeted IQVIA Prime/Partner network site utilization and site performance metrics through efficient site identification
  • Supports achievement of R&DS target for Tier 1+ High Priority sites through efficient site identification
  • In collaboration with strategy and operational teams, supports the development of materials related to site strategies for internal customers and for inclusion in customer facing materials. Provides summaries of site strategy details to position IQVIA to win new business
  • Contributes to the process improvement by actively proposing resolution to issues and providing recommendations for solutions to deliver quality and consistency
  • Proactively contributes to technology/tool development by identifying areas of improvement and providing recommendations for enhancements to deliver quality and consistency
  • Contributes to management of Business Conflicts of Interest (BCOIs)
  • Maintains regular communication with staff in assigned therapeutic areas on non-project issues such as development of therapeutic networks, business strategy, pipelines / planning performance trends across all studies
  • Contributes to the development of Site Intelligence/Site ID sections in sponsor manuals for selected partnership accounts
  • May provide training and support to new team members
  • Performs other tasks as required from time to time

Qualifications
  • Bachelor’s Degree Healthcare or Biological Science Req
  • 1 years’ relevant experience in clinical research. Equivalent combination of education, training and experience.
  • Clinical/project management experience is preferred.
  • General knowledge and understanding of company clinical systems, procedures and corporate standards.
  • Working knowledge of medical terminology, GCP, FDA regulations, and Drug Development process.
  • Sound understanding of clinical research.
  • Effective communication, organizational and interpersonal skills.
  • Strong computer literacy, including well-developed computer skills in applicable software.
  • Ability to work independently and effectively prioritize tasks.

IQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry. 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. Learn more at https://jobs.iqvia.com


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