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Sql Clinical Research Jobs (NOW HIRING)

Zipongo

Clinical Research Scientist

San Francisco, CA · On-site

We are looking for an outstanding Clinical Research Scientist with strong human subjects research ... Experience with SQL. Expertise in epidemiology, biostatistics, and use of observational, real world ...

Zipongo

Clinical Research Scientist

San Francisco, CA

We are looking for an outstanding Clinical Research Scientist with strong human subjects research ... Experience with SQL. Expertise in epidemiology, biostatistics, and use of observational, real world ...

Promedica

Clinical Research Scientist

Toledo, OH

As the Clinical Research Scientist, you implement investigator-initiated clinical research studies ... Statistical, analysis background with experience in SQL databases, experience in medical writing.

Washington University of St. Louis

$75K - $128K/yr

Leadership of the Functional Research Groups * Makes hiring and staffing decisions in the ... SQL Databases, Stress Management, Written Communication Grade G14 Salary Range $75,200.00 - $128 ...

Tufts Medicine

... SQL for querying large relational databases. 4. Experience with programming languages for data ... Knowledge of clinical research processes and study design. Duties and Responsibilities: The duties ...

Integrated Resources INC

Oracle PL/SQL Developer

Edison, NJ · On-site

$52.50 - $66.25/hr

Information Technology (IT), Clinical Research, Rehabilitation Therapy and Nursing. Responsibilities As an Oracle PL/SQL Developer, you will be a key member of the Database Group responsible for ...

University of Utah

Hourly Research Assistants

Campus, IL · On-site

$13.82 - $26.94/hr

Develop, maintain, and optimize data processing pipelines for clinical and research datasets using Python and SQL. * Assist with the design, training, and evaluation of machine learning models ...

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Sql Clinical Research information

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$13

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How much do sql clinical research jobs pay per hour?

As of Aug 1, 2026, the average hourly pay for sql clinical research in the United States is $24.09, according to ZipRecruiter salary data. Most workers in this role earn between $20.19 and $24.76 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as an SQL Clinical Research professional, and why are they important?

To thrive as an SQL Clinical Research professional, you need a strong understanding of clinical research methodologies, database management, and SQL querying, typically supported by a degree in life sciences, computer science, or a related field. Experience with clinical data management systems (such as Medidata or Oracle Clinical) and certifications in clinical research or data analytics are highly valued. Analytical thinking, attention to detail, and effective communication are crucial soft skills for interpreting complex data and collaborating with multidisciplinary teams. These skills ensure data integrity, regulatory compliance, and actionable insights that advance clinical research outcomes.

What are SQL Clinical Research professionals?

SQL Clinical Research professionals are specialists who use SQL (Structured Query Language) to manage, analyze, and report data collected in clinical research studies. They work with large healthcare databases to ensure data quality, extract meaningful insights, and support clinical trials by generating reports and datasets needed for regulatory submissions. Their role is vital in ensuring accurate data analysis, which helps in making informed decisions about the safety and effectiveness of medical treatments.

What is the difference between Sql Clinical Research vs Clinical Data Coordinator?

AspectSql Clinical ResearchClinical Data Coordinator
Required CredentialsSQL certification, clinical research trainingClinical research certification, data management training
Work EnvironmentResearch organizations, pharmaceutical companiesHospitals, research sites, clinical trial centers
Employer & Industry UsageUsed for database management and analysis in clinical trialsManages and verifies clinical trial data at sites
Common Search & ComparisonFocuses on data analysis and database skillsFocuses on data entry, verification, and management

Sql Clinical Research professionals primarily handle database management and data analysis using SQL in clinical trials, often working in research organizations. Clinical Data Coordinators focus on managing and verifying clinical trial data at research sites. While both roles require knowledge of clinical research processes, Sql Clinical Research emphasizes data analysis skills, whereas Clinical Data Coordinators focus on data accuracy and entry.

How does a SQL Clinical Research professional typically collaborate with clinical and data teams during a research study?

As a SQL Clinical Research professional, you will work closely with clinical teams, data managers, and biostatisticians to ensure seamless data collection, cleaning, and analysis. Your main responsibilities involve designing and running SQL queries to extract and validate study data, addressing data discrepancies, and generating reports for stakeholders. Collaboration is key, as you'll regularly participate in team meetings, clarify data requirements, and support clinical staff in understanding database structures and results, ensuring that research objectives are met efficiently and compliantly.
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Sql Clinical Research jobs near you
Infographic showing various Sql Clinical Research job openings in the United States as of July 2026, with employment types broken down into 2% As Needed, 73% Full Time, 17% Part Time, and 8% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $50,108 per year, or $24.1 per hour.

Clinical Research Analyst III - Clinical Research Hub

University of Florida

Gainesville, FL • On-site

$75K - $85K/yr

Full-time

Posted 20 days ago

University Of Florida rating

7.2

Company rating: 7.2 out of 10

Based on 108 frontline employees who took The Breakroom Quiz

383rd of 614 rated colleges and universities

Job description

Clinical Research Analyst III - Clinical Research Hub
Job no: 540534
Work type: Staff Full-Time
Location: Main Campus (Gainesville, FL)
Categories: Grant or Research Administration, Health Care Administration/Support
Department:29011701 - MD-OR CLINICAL RESEARCH HUB
Classification Title:
Clinical Research Analyst III
Classification Minimum Requirements:
Bachelor's degree in an appropriate area and three years of relevant experience; or an equivalent combination of education and experience.
Job Description:
The University of Florida Clinical Research Hub is seeking an experienced OnCore Systems Administrator / Clinical Research Team Lead to support and enhance clinical research operations through the configuration, administration, maintenance, and optimization of the OnCore Clinical Trials Management System (CTMS). In this key leadership role, you will ensure system integrity, regulatory compliance, and alignment with institutional workflows while serving as the team lead and direct supervisor for an assigned Clinical Research Analyst II (CRA II).
Working collaboratively with clinical research staff, finance, and IT teams, you will manage protocol builds, billing compliance, reporting, system integrations (including Epic), and workload coordination for your assigned team member. As the OnCore subject matter expert, you will provide training, supervision, user support, and process improvement leadership to enhance system utilization, operational consistency, and the successful execution of clinical research across the institution
More about this position:
OnCore System Administration and Team Lead Oversight
  • Configure and maintain OnCore CTMS, including user roles, permissions, system dictionaries, protocol configuration, and system upgrades.
  • Monitor system performance, troubleshoot issues, and serve as the team lead for day-to-day OnCore administration activities.
  • Assign, prioritize, and review work performed by the assigned CRA II direct report to ensure accurate, timely, and compliant completion of CTMS-related tasks.

Protocol & Calendar Build Support
  • Build and maintain study calendars, coverage analyses, and protocol records.
  • Collaborate with study teams to ensure accurate study setup and compliance with billing and regulatory requirements.
  • Provide direct guidance, quality review, and escalation support to the CRA II direct report on protocol build activities, calendar maintenance, and related workflow questions.

Data Integrity, Reporting, and Quality Review
  • Ensure data accuracy and completeness within OnCore.
  • Develop and maintain reports, dashboards, and data extracts for operational, financial, and compliance tracking.
  • Conduct audits and quality assurance checks, including review of work completed by the CRA II direct report, and implement corrective action or additional training when needed.

Training, User Support, and Staff Supervision
  • Provide onboarding, training, and ongoing support to OnCore users.
  • Develop SOPs, user guides, and training materials.
  • Serve as a subject matter expert for system-related inquiries.
  • Provide direct supervision to the assigned CRA II, including work direction, coaching, performance feedback, and support for professional development in coordination with departmental leadership.

System Integration and Process Improvement
  • Support integrations with EPIC and other institutional systems.
  • Identify workflow improvements, participate in system upgrades, and implement enhancements to optimize system use.
  • Lead process improvement efforts involving OnCore workflows and coordinate implementation activities with the CRA II direct report and other stakeholders.

Expected Salary:
$75,000 - $85,000 annually
Required Qualifications:
Bachelor's degree in an appropriate area and three years of relevant experience; or an equivalent combination of education and experience.
Preferred:
The ideal candidate will possess:
  • Bachelor's degree in information systems, health informatics, clinical research, or related field; or equivalent combination of education and experience
  • Minimum of three (3) years of experience in clinical research operations, CTMS administration, or healthcare IT systems
  • Experience with clinical trial workflows and regulatory requirements (FDA, NIH, GCP)
  • Direct experience administering OnCore CTMS
  • Experience with OnCore calendar builds and coverage analysis
  • Familiarity with EPIC research billing integration
  • Experience with reporting tools (SQL, Power BI, Tableau)
  • CCRP, CCRC, or equivalent clinical research certification
  • Experience in an academic medical center or large research institution
  • Experience serving as a team lead, supervisor, or work lead in a clinical research, CTMS, or healthcare operations setting
  • Experience training, coaching, assigning work, and reviewing deliverables for clinical research staff or analysts

Special Instructions to Applicants:
Applicants must upload a copy of the following documents to be considered for this position:
Cover Letter or Letter of Interest
Curriculum Vitae or Resume
List of Three Professional References
Application must be submitted by 11:55 p.m. (ET) of the posting end date.
This requisition has been extended. Previous applicants are still under consideration and need not apply.
Health Assessment Required:No
Advertised: 13 Jul 2026 Eastern Daylight Time
Applications close: 10 Aug 2026 Eastern Daylight Time
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About University of Florida

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The University of Florida is one of the top ranked public universities in the United States (ranked top 5 amongst public universities in 2023 US news and world report). It is one of only a few comprehensive universities, having medical, veterinary, dental, nursing, public health, and engineering disciplines all co-localized on the same, contiguous campus to facilitate interdisciplinary collaboration. Gainesville is located in the northern region of Florida, within 1-1.5 hours of each coast, and just 1.5-2 hours to Orlando and Tampa. It is a small to medium-sized city with a low cost of living, excellent public and private schools, and southern hospitality. While Gainesville is widely recognized as the home of the Gators, it is quickly becoming known as a center for innovation and a place with a lifestyle that's comfortable for families, yet attractive for young professionals.

Industry

Colleges, universities, and professional schools

Company size

5,001 - 10,000 Employees

Headquarters location

Gainesville, FL, US

Year founded

1853

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