Senior Data Analyst, Clinical Trials Feasibility Senior Data Analyst, Clinical Trials Feasibility This position is full-time and home-based anywhere in the United States or Canada. Candidates located on West Coast/PST time zone strongly preferred. Candidates who can work hybrid in San Francisco, CA office strongly preferred but not required Relocation assistance not provided at this time. Summary: IQVIA’s FSP team is seeking an experienced Senior Clinical Data Analyst to join an Advanced Analytics group within our clients Clinical Data Science department. The ideal candidate will have 5+ years of relevant experience supporting clinical trial operations as a data analyst on tasks such as study feasibility, design optimization, site selection, etc . Use tools or SQL databases to get data and then format and communicate it in a way that study teams can understand the insights. Previous experience supporting efforts for clinical trials is required, such as providing data-driven insights used in making decisions. Responsibilities: Support Clinical Operational Strategy by using Python and SQL to query, aggregate, analyze, and derive results from clinical trial operations data. Collaborate with clinical study teams to understand their analytics needs, perform analyses, and report back with tailored results with minimal oversight. Work with real-world data modalities such as Medical Claims, Electronic Health Record data. Develop, maintain, and enhance models, tools, and visualizations to support ongoing or planned clinical trials. Ensure data quality and integrity through all work. Communicate complex analytical findings in a clear and concise manner to both technical and non-technical stakeholders. Provide feedback to product managers for internal systems to do operational strategy Ability to apply statistical models and advanced analytical techniques Requirements: Bachelor's degree in a field related to data science, engineering, computer science, statistics, or machine learning. Relevant years of experience will be considered in lieu of a degree 5+ years of relevant experience in supporting the operational feasibility, design analytics, and analytics of clinical trial operations. Strong proficiency in both Python and SQL for data querying, aggregation, and analysis. Experience working at a Clinical Research Organization or Pharmaceutical company conducting study feasibility and site selection analytics required Strong skills in Excel and PowerPoint. Adaptable and comfortable with using new tools as required Demonstrated ability to engage and work with clinical study teams to understand their needs and deliver results. Strong communication skills, with the ability to communicate complex analytical findings in a clear and concise manner to both technical and non-technical stakeholders. . 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 IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe The potential base pay range for this role, when annualized, is $88,300.00 - $273,200.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits. Senior Data Analyst, Clinical Trials Feasibility This position is full-time and home-based anywhere in the United States or Canada. Candidates located on West Coast/PST time zone strongly preferred. Candidates who can work hybrid in San Francisco, CA office strongly preferred but not required Relocation assistance not provided at this time. Summary: IQVIA’s FSP team is seeking an experienced Senior Clinical Data Analyst to join an Advanced Analytics group within our clients Clinical Data Science department. The ideal candidate will have 5+ years of relevant experience supporting clinical trial operations as a data analyst on tasks such as study feasibility, design optimization, site selection, etc . Use tools or SQL databases to get data and then format and communicate it in a way that study teams can understand the insights. Previous experience supporting efforts for clinical trials is required, such as providing data-driven insights used in making decisions. Responsibilities: Support Clinical Operational Strategy by using Python and SQL to query, aggregate, analyze, and derive results from clinical trial operations data. Collaborate with clinical study teams to understand their analytics needs, perform analyses, and report back with tailored results with minimal oversight. Work with real-world data modalities such as Medical Claims, Electronic Health Record data. Develop, maintain, and enhance models, tools, and visualizations to support ongoing or planned clinical trials. Ensure data quality and integrity through all work. Communicate complex analytical findings in a clear and concise manner to both technical and non-technical stakeholders. Provide feedback to product managers for internal systems to do operational strategy Ability to apply statistical models and advanced analytical techniques Requirements: Bachelor's degree in a field related to data science, engineering, computer science, statistics, or machine learning. Relevant years of experience will be considered in lieu of a degree 5+ years of relevant experience in supporting the operational feasibility, design analytics, and analytics of clinical trial operations. Strong proficiency in both Python and SQL for data querying, aggregation, and analysis. Experience working at a Clinical Research Organization or Pharmaceutical company conducting study feasibility and site selection analytics required Strong skills in Excel and PowerPoint. Adaptable and comfortable with using new tools as required Demonstrated ability to engage and work with clinical study teams to understand their needs and deliver results. Strong communication skills, with the ability to communicate complex analytical findings in a clear and concise manner to both technical and non-technical stakeholders. . 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 IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe The potential base pay range for this role, when annualized, is $88,300.00 - $273,200.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits. About the company IMS Health and Quintiles are now IQVIA. We are committed to providing solutions that enable healthcare companies to innovate with confidence, maximize opportunities and, ultimately, drive healthcare forward. We do this via breakthroughs in insights, t... Notice Talentify is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or protected veteran status. Talentify provides reasonable accommodations to qualified applicants with disabilities, including disabled veterans. Request assistance at accessibility@talentify.io or 407-000-0000. Federal law requires every new hire to complete Form I-9 and present proof of identity and U.S. work eligibility. An Automated Employment Decision Tool (AEDT) will score your job-related skills and responses. Bias-audit & data-use details: www.talentify.io/bias-audit-report . NYC applicants may request an alternative process or accommodation at aedt@talentify.io or 407-000-0000.

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