Clinical Research Data Analyst

Overview

 

• Consecutively recognized as a top employer by Forbes, and in 2025 by Newsweek 

• Free Continuing Education and certification including BLS, ACLS and PALS 

• Tuition reimbursement, education programs and scholarships 

• Vacation time starts building on Day 1, and builds with your seniority 

• Free money toward retirement with a 403(b) and matching contributions 

• Great food options with on-demand ordering 

• Free parking and electric charging 

 

Commitment to diversity and inclusion is a cornerstone of our culture at Community. All are welcome as valued members of our community. 

We know that our ability to provide the highest level of care is through taking care of our incredible teams. Learn more on our Benefits page. 

Responsibilities

The Clinical Research Analyst is responsible for performing feasibility analysis on incoming research studies to ensure adherence to good clinical practice guidelines, state and federal regulations, and institutional policies and procedures related to research activity. A feasibility analysis takes all of a research proposal's relevant factors into account (e.g., research billing, compliance/privacy, technical knowledge of EMR, data management, legal), along with clinical operational considerations to ascertain the likelihood of completing the research project or clinical trial successfully. Feasibility analysis of a study can be a comprehensive strategy designed to prevent, discover, or defend against corporate misconduct and can determine how a business will operate. This analysis will provide critical information of any potential problems that may arise so we may mitigate risk.  Demonstrates a strong understanding of clinical operations, data management, privacy, and compliance standards for research. Assists the department in meeting regulatory requirements, quality metrics through functions such as data aggregation, analysis, and report generation for research; electronic and paper file management; performance improvement tracking and reporting of outcomes; benchmarking research and associated activities; coordination of special projects; and facilitation and development of research report requesting by PIs and study teams.

 

The role is not about conducting a single research project; it is about facilitating research for others across the organization. 

• Data Intake & Guidance: Reviewing protocols and meeting with study teams to define data needs. 

• Consultative Coaching: Guiding researchers who may not understand certain data (like free text in Epic) is difficult to pull. Helping them define patient populations and measurable data points. 

• Liaison Work: Coordinating with Revenue Cycle (Chargemasters), IS (Epic builds), and Central Services. 

• Technical Execution: Extracting data from EMR systems and performing statistical analysis. 

 

* This position may start off as a remote position but will eventually transition to a full-time onsite position in Downtown Fresno, near CRMC.*

  

Qualifications

Education

• Bachelor's Degree in Healthcare, Business, or relevant field required
• Master's Degree preferred

 Experience

• 2 years of experience writing reports and summarizing data required
• Previous experience in healthcare, research, data analysis, performance improvement, quality management activities, and/or project management preferred
• Prior experience querying EMR clinical data warehouses (e.g., Epic Clarity/Caboodle) preferred 
• Data request intake experience preferred
• Experience performing statistical evaluation of clinical data to ensure accuracy and regulatory compliance.

 

Disclaimers

• Pay ranges listed are an estimate and subject to change.• If any bonuses are noted, they are only applicable to external hires meeting criteria.