Clinical Trial Feasibility Analyst

Regulatory Toolkit; United States; Remote; USD 88,000 - 221,000; Full time

Job summary

IQVIA is seeking an experienced Clinical Data Analyst to join our Advanced Analytics group within the Clinical Data Science department. You will support clinical trial operations for a pharmaceutical client, applying Python and SQL to query, analyze, and visualize data for study teams.

The ideal candidate has 3+ years in clinical trial analytics, strong communication skills, and the ability to translate complex data findings into actionable insights for both technical and non-technical

Qualifications

• 3+ years of relevant experience in supporting the operational feasibility, design, and analytics of clinical trial operations.
• Strong proficiency in Python and SQL for data querying, aggregation, and analysis.
• Experience supporting efforts for clinical trials is required, such as providing insights used in making decisions within clinical trials.
• Cloud experience (such as AWS or DataBricks) is preferred but not required.
• Excellent problem-solving and communication skills.
• Ability to communicate findings to technical and non-technical audiences.

Responsibilities

• Query, aggregate, analyze, and derive results from clinical trial operations data using Python and SQL.
• Collaborate with clinical study teams to understand analytics needs and deliver tailored results.
• Develop, maintain, and enhance models, tools, and visualizations for ongoing or planned trials.
• Ensure data quality and integrity throughout all work.
• Present findings clearly to stakeholders.

Skills

Python

SQL

Data analysis

Communication skills

Education

Bachelor's or Master's in data science / engineering / CS / statistics / ML

Tools

AWS

Databricks

Job description

Location: Home-based

Summary

We are seeking an experienced Clinical Data Analyst to join an Advanced Analytics group within the Clinical Data Science department. Have dedicated efforts to one of our Pharmaceutical clients, focused on their initiatives in data analytics. The ideal candidate will have 3+ 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. Experience supporting efforts for clinical trials is required, such as providing insights used in making decisions within clinical trials.

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.


• 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.

Requirements

• Bachelor's or Master's degree in a field related to data science, engineering, computer science, statistics or machine learning.


• 3+ years of relevant experience in supporting the operational feasibility, design, and analytics of clinical trial operations.


• Experience supporting efforts for clinical trials is required, such as providing insights used in making decisions within clinical trials.


• Strong proficiency in both Python and SQL for data querying, aggregation, and analysis.


• Cloud experience (such as by using AWS or DataBricks) is preferred but not required.


• Demonstrated ability to engage and work with clinical study teams to understand their needs and deliver results.


• Excellent problem-solving skills with the ability to analyze complex datasets and derive actionable insights.


• Strong communication skills, with the ability to present data-driven findings to both technical and non-technical audiences.


• Ability to author e-mails summarizing key KPI’s or insights and putting together slides to summarize the results of analysis.

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

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

The potential base pay range for this role, when annualized, is $88,300.00 - $220,900.00. 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.