Clinical Trials Feasibility Analyst

IQVIA; North Carolina; Hybrid; USD 88,000 - 221,000; Full time

Job summary

IQVIA is seeking an experienced Clinical Trials Feasibility Analyst to join an Advanced Analytics group within the Clinical Data Science department. The role focuses on study feasibility analytics for a Pharmaceutical client, requiring 5+ years of relevant experience in operational feasibility, design optimization, and site selection.

The ideal candidate will have strong Python and SQL skills, experience with real-world data such as Medical Claims and EHR data, and the ability to translate

Qualifications

• Bachelor’s or Master’s degree in a field related to data science, engineering, computer science, statistics or machine learning. Working experience can be considered in lieu of a degree.
• 5+ years of relevant experience in supporting the operational feasibility, design, and analytics of clinical trial operations.
• Experience at a CRO or pharmaceutical company conducting study feasibility and site selection analytics.

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 analytics needs, perform analyses, and report back with tailored results with minimal oversight.
• Work with real-world data modalities such as Medical Claims and Electronic Health Record data.
• Use tools or SQL databases to get data and communicate it so study teams can understand insights.
• Ensure data quality and integrity through all work.
• Communicate complex analytical findings clearly to both technical and non-technical stakeholders.

Skills

Python

SQL

Excel

PowerPoint

Education

Bachelor’s or Master’s in data science / engineering / CS / statistics

Job description

Summary:

Our IQVIA team is seeking to hire an experienced Clinical Trials Feasibility Analyst to join an Advanced Analytics group within the Clinical Data Science department. Join this team dedicated to a Pharmaceutical client, focused on efforts in study feasibility analytics. 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 and site selection. Previous e xperience supporting these types of analytics for clinical trials is required.

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.
• Use tools or SQL databases to get data and then format and communicate it in a way that study teams can understand the insights.
• 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. Working experience can be considered in lieu of a degree.
• 5+ years of relevant experience in supporting the operational feasibility, design, and analytics of clinical trial operations. Less years of working experience can be considered if the individual can commit to a hybrid work schedule onsite in South San Francisco.
• Experience working at a Clinical Research Organization or Pharmaceutical company conducting study feasibility and site selection analytics.
• Strong skills in Excel and PowerPoint.
• Moderate proficiency in both Python and SQL for data querying, aggregation, and analysis.
• Experienced in real-world data modalities such as Medical Claims, Electronic Health Record data.
• Experience communicating country, site, investigator, patient insights, KoL insights and other analysis to clinical trial teams.
• Solid understanding of clinical development process is expected.

Location:

Individuals located in the U.S. or Canada can be considered. Preference for individuals in the west coast time zone.

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.