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The Associate Design Analytics Lead defines data needs, conducts design analytics, and develops and delivers reports and structured outputs to support protocol assessments and trial design decision making. This role involves utilizing multiple data sources for analysis, developing data storyboards, collaborating internally to create meaningful client insights and reports, and presenting to stakeholders. You will also train and support new team members or junior staff, recommend process improvements, and contribute to innovation. This an individual contributor role.

Responsibilities

• Ensure IQVIA planning services provide a competitive edge in winning new business.
• Independently deliver accurate and robust protocol assessments for various opportunities, including RFPs, early engagements, re-bids, and awarded studies.
• Support the development of materials related to protocol assessments for clients, bid defense meetings, and internal customers.
• Collaborate with key stakeholders and IQVIA project teams to resolve issues.
• Conduct research into therapeutic areas and draft data storyboards and insights reports for insights meetings.
• Lead insights meetings with internal stakeholders, present data analysis results, and finalize client reports.
• Train and support new team members.
• Demonstrate proficiency with insights tools and understand system features to accomplish accurate protocol assessments and strategies.
• Develop and present complete client deliverables within established frameworks and methodologies.
• Proactively develop knowledge of consulting methodologies through engagements and learning opportunities.
• Manage project timelines and day-to-day communication with stakeholders.

Requirements

• Approximately 3 years of relevant experience in clinical research or an equivalent combination of education, training, and experience.
• Intermediate knowledge of principles, theories, and concepts in the job area, typically obtained through advanced education and experience.
• Bachelor's Degree in Healthcare or Biological Science.
• Preferred clinical/project management experience.
• General knowledge of company clinical systems, procedures, and corporate standards.
• Good knowledge of medical terminology, GCP, FDA regulations, and the drug development process.
• In-depth understanding of clinical research.
• Excellent communication, organizational, and interpersonal skills.
• Proficient report writing in English.
• Strong computer literacy and well-developed skills in applicable software.
• Ability to work independently and effectively prioritize tasks.

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com