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Oracle Clinical Jobs (NOW HIRING)

Intego Group

NY · On-site

$90 - $120/hr

Must demonstrate intermediate UNIX, Oracle Clinical or equivalent clinical DM system, and relational database theory. * Track record of generating new ideas and solutions to data analysis. * Thorough ...

Integrated Resources INC

Oracle Programmer

Horsham, PA · On-site

Information Technology (IT), Clinical Research, Rehabilitation Therapy and Nursing. Position: Oracle Programmer Location: Horsham PA Duration: 10+ Months The Safety Data Programmer is responsible for ...

Nordic

Senior Clinical Consultant - Oracle Health The Senior Consultant provides consulting services to clients on Oracle Health-related projects. You will provide subject matter expertise during client ...

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How much do oracle clinical jobs pay per hour?

As of Sep 4, 2026, the average hourly pay for oracle clinical in the United States is $57.64, according to ZipRecruiter salary data. Most workers in this role earn between $39.66 and $70.19 per hour, depending on experience, location, and employer.

What is Oracle Clinical?

Oracle Clinical is a comprehensive clinical data management system used by pharmaceutical and biotechnology companies to manage and analyze clinical trial data. It helps streamline the process of data collection, validation, and reporting, ensuring compliance with regulatory standards. The system supports the design of data entry screens, management of clinical data, and generation of reports for regulatory submissions. Oracle Clinical is widely used in the industry due to its robust data management capabilities and integration with other clinical trial tools.

What are the typical daily responsibilities of an Oracle Clinical professional in a clinical trials environment?

An Oracle Clinical professional is commonly responsible for designing and managing clinical trial databases, ensuring accurate data capture, and supporting data validation activities. Daily tasks often include configuring study protocols within the system, monitoring data quality, troubleshooting system issues, and collaborating closely with clinical data managers, statisticians, and regulatory teams. They may also be involved in user training, system upgrades, and generating reports to facilitate trial progress. The role requires attention to detail, strong communication skills, and the ability to work within multidisciplinary teams to ensure compliance with regulatory standards.

What are the key skills and qualifications needed to thrive as an Oracle Clinical specialist, and why are they important?

To thrive as an Oracle Clinical specialist, you need a solid background in clinical data management, database administration, and an understanding of clinical trial processes, often supported by a degree in life sciences or information technology. Expertise in Oracle Clinical software, SQL, and experience with electronic data capture (EDC) systems and regulatory compliance are typically required. Strong analytical thinking, attention to detail, and effective communication skills are crucial for ensuring data integrity and collaborating with cross-functional teams. These competencies are vital to maintaining accurate clinical trial data, meeting regulatory standards, and supporting successful drug development processes.

What is the difference between Oracle Clinical vs Clinical Data Manager?

AspectOracle ClinicalClinical Data Manager
Primary RoleDevelops and manages clinical trial data collection systems using Oracle Clinical softwareOversees data management processes, ensuring data quality and integrity in clinical trials
Required SkillsKnowledge of Oracle Clinical, database management, clinical trial processesData management expertise, familiarity with clinical software, attention to detail
Work EnvironmentPharmaceutical companies, CROs, clinical research settingsClinical research organizations, pharmaceutical companies, biotech firms
CertificationsOracle Clinical certifications, clinical research certifications

Oracle Clinical professionals focus on developing and maintaining clinical trial data systems, while Clinical Data Managers oversee the overall data quality and management processes. Both roles require familiarity with clinical data software and work within similar environments, but their responsibilities differ in scope and focus.

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Oracle Clinical jobs near you
Infographic showing various Oracle Clinical job openings in the United States as of August 2026, with employment types broken down into 3% As Needed, 71% Full Time, 18% Part Time, and 8% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $119,901 per year, or $57.6 per hour.

Senior/Principal Clinical Statistical Programmer

Intego Group

NY • On-site

$90 - $120/hr

Other

Posted 17 days ago

Job description

Senior/Principal Clinical Statistical Programmer

USA

Intego Clinical’s office in Florida, USA, is looking for experienced Senior/Principal Clinical Statistical Programmers to join our global team working from the office or remotely.

As a clinical project team member, the Senior/Principal Clinical Statistical Programmer applies advanced‑level programming techniques and leadership to the planning, design, development, implementation, and maintenance of software for the monitoring, reporting, and analysis of clinical trials.

Job responsibilities:

The Senior/Principal Clinical Statistical Programmer will be responsible for overall timelines and significant project milestones, and overall project quality, integrity, and productivity. May serve on or lead a departmental initiative, specialized projects, and working groups. Can serve as a project team leader. This senior position should be capable of developing and maintaining software development tools and standard templates. Also, this person should be a Subject Matter Expert (SME) as a technology troubleshooter.

  • Responsible for the processing of clinical data required for analysis of clinical trials for Phase 1‑4.
  • Develop SAS coding and table templates for preparing, processing, and analyzing clinical data.
  • Generate and QC summary tables, data listings, and graphs for in‑house analyses of study data or publications using SAS standard coding practices.
  • Create/acquire tools to improve programming efficiency or quality.
  • Validate the work of other programmers/analysts.
  • Create/review programming plan, specifications for datasets, and TLF’s.
  • Establish monitoring of data transfers for ongoing trials to identify study conduct or data quality issues.
  • Support data queries from other functional groups (Biostatistics, Medical Writing, Clinical Development, Clinical Operations, Regulatory, and Marketing).
General requirements:
  • A minimum of a Bachelor’s degree in Computer Science, Mathematics, Statistics, Pharmaceuticals Sciences, Life Sciences, and related areas is required. A Master’s is preferred.
  • A minimum of 4 years of hands‑on relevant career experience in the pharmaceutical or biotechnology industry.
  • Have excellent knowledge of SAS programming and associated features and their applications in the pharmaceuticals industry environment, particularly clinical trial data sets.
  • Familiar with CDISC conventions, i.e., SDTM and ADaM models, and hands‑on experience implementing these models.
  • Strong understanding of clinical trial data and hands‑on in data manipulations, analysis, and reporting of analysis results.
  • Must understand the role of all the functional areas in the clinical trial process.
  • Must have a basic understanding of the FDA/ICH guidelines, the software development life cycle, 21 CFR Part 11, and other relevant FDA regulations.
  • Must possess the knowledge and application of p‑values, confidence intervals, linear regression analysis, advanced general linear models, frequencies, survival analysis, non‑parametric analysis, randomization software, and demonstrate proficiency in implementing new ideas in clear, efficient SAS code for the purposes of data analysis and reporting.
  • Must demonstrate intermediate UNIX, Oracle Clinical or equivalent clinical DM system, and relational database theory.
  • Track record of generating new ideas and solutions to data analysis.
  • Thorough understanding of relational database components and theory.
  • SAS certification is an advantage.
  • It would be an asset to have had experience working on FDA submissions.
  • The candidate should demonstrate clear and timely written and verbal communication with peers, customers, and management.
  • Should be able to present effective presentations to small groups such as Project Teams or during Statistical Programming meetings.
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