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The 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 both internal and external stakeholders. Additionally, the successful candidate will train and mentor junior staff and country leads, recommend process improvements, and may lead innovations.

Responsibilities:

• Ensure IQVIA planning services provide a competitive edge in securing new business.
• Independently create complex protocol assessments, country and/or enrollment strategies, or site lists for various opportunities, including requests for proposals, early engagements, re-bids, and awarded studies.
• Support the development of materials related to protocol assessments for clients, bid defense meetings, and internal customers.
• Conduct complex research into therapeutic areas and draft data storyboards and insights reports for insights meetings.
• Lead complex insights meetings with internal stakeholders, present data analysis results, and finalize client reports.
• Train, support, and mentor new team members.
• Serve as a Subject Matter Expert (SME) for insights tools, demonstrating a deep understanding of system features and functions to accomplish accurate protocol assessments and strategies.
• Deliver findings to clients as needed.
• Recommend improvements and alternative solutions to resolve problems.
• Proactively develop broader and deeper knowledge of consulting methodologies through on-the-job experience and training opportunities, and begin to develop CoE-specific subject matter expertise.
• Manage project timelines and day-to-day communication with stakeholders.

Requirements:

• Approximately 3-5 years of relevant experience in clinical research or an equivalent combination of education, training, and experience.
• Extensive 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