Associate Clinical Information Analyst

Abbott

. Participate in discussions with Site Management, Study Management, Data Review, Safety, and other shared service functions to gather operational, analytical, and study-specific reporting requirements .

Posted 9/16/2026full-timeMaple Grove • California • United StatesJuniorMid-Level💰 $50,700 - $101,300 per yearWebsite

Core Competencies

Role fit

Core Competencies

Use this summary to align your resume positioning with the role.

Demonstrates expertise in SQL query development, reporting solutions, and data visualization using Power BI, while adhering to Good Clinical Practices and FDA regulations. Proficient in supporting clinical trial databases and enhancing reporting portfolios in a collaborative environment.

Highest-signal resume keywords

SQL Query DevelopmentPower BI VisualizationOracle RDBMSClinical Trial Database SupportGood Clinical Practices

ATS Keywords

Tailor your resume

Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills

SQLDatabase Management SystemsData VisualizationClinical Trial Management SoftwareOracle ClinicalPythonAgile DevelopmentStatisticsData ScienceDatabase Terminology

Soft Skills

Organizational SkillsAttention to DetailStrong Communication SkillsTeam CollaborationProject Management

Tools & Technologies

Microsoft OfficePower BITableauOracle RDBMSClinical Trial Management Software

Industry Keywords

Good Clinical PracticesFDA RegulationsClinical TrialsHealth SciencesHuman Physiology

Tech Stack

Tools & technologies

OraclePythonRDBMSSQLTableau

About the role

Key responsibilities & impact

Participate in discussions with Site Management, Study Management, Data Review, Safety, and other shared service functions to gather operational, analytical, and study-specific reporting requirements
Support development of reporting solutions, primarily SQL queries in Oracle RDBMS and Power BI visualizations
Support ongoing maintenance and enhancement of the reporting portfolio
Conduct peer review and quality control of products
Support and train end-users of the reporting portfolio
Support development and standardization of reporting conventions
Work under Good Clinical Practices, Good Clinical Data Management Practices, and FDA regulations and guidelines

Requirements

What you’ll need

Bachelor’s degree in Computer Science, Health Sciences or related field, or an equivalent combination of education and work experience
Organizational and basic project management skills
Attention to detail
Highly skilled with Microsoft Office products including Word, Excel, and Access
Basic ability to work with database management systems
Basic knowledge of database terminology and technology
Basic knowledge and experience supporting the building of clinical trial databases using Oracle Clinical or equivalent
Basic knowledge and experience building/customizing Clinical Trial Management Software Applications
Ability to work in a highly matrixed and geographically diverse business environment
Ability to work within a team and as an individual contributor in a fast-paced, changing environment
Strong oral and written communication skills
Ability to meet deadlines and handle multiple assignments in a timely manner
Basic understanding of human physiology or prior involvement with the medical field
Preferred: Experience in Agile Development
Preferred: Working knowledge in Data Science, Statistics, data visualization tools such as Power BI and Tableau
Preferred: Experience with SQL, Python, Vega/Vega-Lite

Benefits

Comp & perks

Career development with an international company
Free medical coverage in the Health Investment Plan (HIP) PPO medical plan for qualifying employees
Retirement savings plan with high employer contribution
Tuition reimbursement
Freedom 2 Save student debt program
FreeU education benefit toward a bachelor’s degree
Health and wellness benefits
Equal Opportunity Employer committed to employee diversity