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Oracle Clinical Jobs in California (NOW HIRING)

Oracle Corporation

Clinical Lab Scientist (CLS)

Manteca, CA · On-site

$59.14 - $91.64/hr

Current/Active California State Licensure as a Clinical Laboratory Scientist. Registered or registry eligible in accordance with an approved certifying agency (ASCP, NCA, AMT or CSMLS within 12 ...

New

Prosum

Cerner Millennium Analyst

Pomona, CA · On-site

$55 - $60/hr

... and knowledge of clinical workflow Expert working knowledge of Cerner modules (PowerChart ... Hands-on experience with Oracle/Cerner design, build, testing, and operational support specifically ...

Sysazzle, Inc

Senior Decision Support Analyst

Los Angeles, CA · On-site

$92K - $114K/yr

... oracle or sql server databases. The job duties and key skills of the job requirement are as follows. • This position is responsible for the creation, design, and maintenance of clinical and ...

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All JobsOracle Clinical JobsOracle Clinical Jobs in California

Oracle Clinical information

See California salary details

$15

$56

$97

How much do oracle clinical jobs pay per hour?

As of Sep 4, 2026, the average hourly pay for oracle clinical in California is $56.45, according to ZipRecruiter salary data. Most workers in this role earn between $38.84 and $68.73 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.

What are popular job titles related to Oracle Clinical jobs in California?

For Oracle Clinical jobs in California, the most frequently searched job titles are:

What job categories do people searching Oracle Clinical jobs in California look for?

The top searched job categories for Oracle Clinical jobs in California are:

Oracle Clinical jobs near you
Infographic showing various Oracle Clinical job openings in California as of August 2026, with employment types broken down into 3% As Needed, 76% Full Time, 14% Part Time, and 7% Contract. Highlights an 94% Physical, 1% Hybrid, and 5% Remote job distribution, with an average salary of $117,411 per year, or $56.4 per hour.

Sr Clinical Programmer

International Executive Service Corps

San Francisco, CA • On-site

$160 - $185/hr

Other

Medical, Dental, Vision, Retirement, PTO

Posted 3 days ago

New

Key responsibilities

  • Develop, implement, and maintain systems and applications that support clinical data management and development operations.

  • Lead the development of standards for data collection, transmission, and review, ensuring compliance with regulatory guidance and CDISC conventions.

  • Oversee vendor activities and coordinate with external and internal teams to ensure consistency in data collection, transmission, and reporting.

Job description

The Sr. Clinical Programmer is an integral member of the CDM team and is responsible for developing, implementing, and maintaining the systems and applications that support CDM and Development Operations across multiple therapeutic areas.

Senior Clinical ProgrammerPosition Summary

Serving as the subject matter expert for data acquisition, archival, interchange, and reporting of clinical research data, this role leads the development of standards for data collection and transmission and collaborates with cross-functional teams to define therapeutic area standards and data review tools. The Senior Clinical Programmer defines best practices for data acquisition, develops company standards aligned with CDISC conventions and regulatory guidance, and maintains a global library of standard forms, edit checks, reports, and data listings. This role directly contributes to the company’s research and development efforts to deliver high-value therapeutics that address unmet medical needs.

• Address highly complex technical problems requiring analysis of nuanced data and intangible variables; exercise independent judgment in developing methods, techniques, and evaluation criteria.

• Provide leadership and direction for database design and programming, systems development and support, and training activities.

• Serve as the EDC and CDISC subject matter expert, providing guidance and best practices to clinical study teams.

• Advise on standards for CRF development, validation, and reporting; implement and maintain standards for data collection, acquisition, archival, and submission in compliance with CDISC and applicable regulatory guidance.

• Oversee EDC development and testing environments; perform functional audits and vendor qualifications.

• Develop and maintain global standards and project-specific specifications, including programming and reporting conventions and rules.

• Define regulatory-compliant data exchange standards with external partners (CROs, central labs, IXRS/IRT, eCOA) and internal teams (Biostatistics, Clinical Operations).

• Oversee vendor activities across multiple trials to ensure consistency in data collection, transmission, and reporting.

• Implement and maintain regulatory-compliant processes for data acquisition, archival, and interchange.

• Coordinate with CROs on data collection instruments and reporting tools and establish tracking mechanisms for process- and system-related issues.

• Mentor team members and contribute to the continuous improvement of CDM processes, tools, and training.

Qualifications & Experience

• Minimum of 8 years of hands-on, relevant experience in the pharmaceutical or biotechnology industry.

• Working knowledge of external data sources (e.g., central labs, IXRS/IRT, eCOA).

• Proficiency in programming and reporting tools such as J-Review, Spotfire, SAS, Java, and C.

• Strong experience with relational databases (SQL Server, Oracle, MySQL, PL/SQL).

• Proficiency in Microsoft Office (Word, Excel, Outlook, PowerPoint).

• Demonstrated proficiency with ICH, GCDMP, CDISC, and GCP guidelines is required.

• Demonstrated ability to solve complex technical problems with innovative solutions.

• Strong organizational, project management, and communication skills.

• Demonstrated ability to develop processes and training materials.

• Self-starter with the ability to mentor others and manage multiple priorities while delivering high-quality work in a dynamic environment.

• Solid understanding of clinical drug development processes preferred.

Education

Bachelor’s degree in Computer Science, Life Sciences, or a related field, or equivalent experience required; advanced degree is a plus.

Additional Information

Nektar currently anticipates the base salary for the Senior Clinical Programmer to range from $160,000 to $185,000 for candidates in the Bay Area and will depend, in part, on successful candidate's location and qualifications for the role, including education and experience. This position will also be eligible for an annual performance bonus in accordance with the terms of the applicable plan (depending, in part, on company and individual performance and at the Company's discretion on an individual basis.) The compensation described above is subject to change and could be higher or lower than the range described based on the market survey data.

Qualifying employees are eligible to participate in benefit programs such as:

  • Health Insurance (Medical/Dental/Vision)
  • Disability Insurance
  • Holiday Pay
  • Paid Time Off (PTO)
  • 401(k) Match
  • Employee Stock Purchase Plan
  • Wellness Programs
  • Parental Leave Benefits (in accordance with the terms of applicable plans)

For general information on company benefits, please go to https://www.nektar.com/careers.

We are an Equal Opportunity Employer and do not discriminate against applicants due to race, ethnicity, gender, veteran status, or on the basis of disability or any other federal, state or local protected class. Nektar Therapeutics will consider for employment qualified applicants with criminal histories in the manner proscribed by the San Francisco Fair Chance Ordinance.

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