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Oracle Clinical Jobs in Texas (NOW HIRING)

Nexa Trials

Data Architect

Austin, TX · On-site

$100 - $130/hr

You will sit at the intersection of eSource, EDC, and sponsor reporting -- defining how data captured in NexaSource™ maps through Nexa Bus™ into Medidata Rave, Veeva, Oracle Clinical One, and ...

Nexa Trials

Senior Sales Executive

Austin, TX · On-site

$100 - $150/hr

Familiarity with Medidata, Veeva, Oracle Clinical One, or competitive eClinical platforms * Experience structuring pilot-to-enterprise expansion deals in regulated industries * Background as a CRA ...

Alpha Consulting Corp.

PL/SQL Developer

Plano, TX · On-site

$48.75 - $61.50/hr

Alpha Consulting Corp. is seeking a highly skilled Oracle PL/SQL Developer to join their team as a ... Alpha Consulting Corp. has been exceeding expectations in the IT, pharmaceutical, and clinical ...

3B Staffing LLC

Epic Sr Bridge/Interfaces Analyst

Murphy, TX · Remote

$84K - $111K/yr

Design and develop clinical and business interfaces in the Epic and/or Oracle Health EMRs according to the project scope and end user workflow with scalability, standard development practices and ...

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Oracle Clinical information

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How much do oracle clinical jobs pay per hour?

As of Sep 5, 2026, the average hourly pay for oracle clinical in Texas is $50.69, according to ZipRecruiter salary data. Most workers in this role earn between $34.88 and $61.73 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 Texas?

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

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

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

Oracle Clinical jobs near you
Infographic showing various Oracle Clinical job openings in Texas as of August 2026, with employment types broken down into 3% As Needed, 72% Full Time, 18% Part Time, and 7% Contract. Highlights an 94% Physical, 1% Hybrid, and 5% Remote job distribution, with an average salary of $105,445 per year, or $50.7 per hour.

Data Architect

Nexa Trials

Austin, TX • On-site

$100 - $130/hr

Other

Re-posted yesterday

Job description

Own the clinical data layer that connects NexaSource capture, Nexa Bus integrations, and sponsor EDC systems — translating protocols and CRFs into durable, standards-aligned schemas that scale across studies.

United States Austin, TX

About the role

Nexa Trials is seeking an experienced Data Architect to design and govern the clinical data models that power our platform and services. You will sit at the intersection of eSource, EDC, and sponsor reporting — defining how data captured in NexaSource™ maps through Nexa Bus™ into Medidata Rave, Veeva, Oracle Clinical One, and custom sponsor environments.

Your work directly reduces duplicate entry, query volume, and study startup friction. You will partner with clinical operations, QC analysts, integration engineers, and AI/automation teams in Lahore to ensure every mapping decision is traceable, GCP-aligned, and maintainable across protocol amendments and multi-site rollouts.

This role is based in Austin, Texas — Nexa Trials headquarters — with flexibility for hybrid or remote work within US time zones. You will report to the Head of Data & Integrations and contribute to our standards roadmap across CDISC, OMOP, and FHIR.

Responsibilities
  • Design end-to-end data models for eSource forms, visit schedules, and Nexa Bus transfer pipelines from protocol and CRF specifications
  • Author and maintain EDC/eSource field mappings, transformation rules, and validation logic for sponsor and CRO study builds
  • Define canonical data structures that support NexaSource capture, NexaScheduler visit events, and downstream analytics
  • Apply CDISC standards (SDTM, ADaM concepts, Define-XML awareness) and evaluate OMOP/FHIR applicability for interoperability initiatives
  • Partner with integration engineers on API contracts, event schemas, and error-handling patterns for live study transfers
  • Review QC findings and query trends to identify systemic mapping gaps and recommend architectural improvements
  • Document data lineage, mapping decisions, and amendment impact assessments for audit-ready sponsor deliverables
  • Contribute to reusable mapping libraries, study templates, and governance processes that accelerate study startup
  • Mentor junior data analysts and collaborate with Clinical AI engineers on structured outputs for LLM-assisted mapping tools
Requirements
  • 5+ years of experience in clinical data architecture, EDC build, or clinical data management on Phase I–IV trials
  • Deep working knowledge of CDISC standards and practical experience translating CRFs into structured clinical datasets
  • Hands‑on experience with EDC/eSource mapping — field‑level transformations, edit checks, and cross‑form dependencies
  • Proficiency with at least two major EDC platforms (e.g., Medidata Rave, Veeva Vault CDMS, Oracle Clinical One, REDCap)
  • Strong SQL skills and familiarity with data integration patterns (REST APIs, flat‑file exchange, ETL pipelines)
  • Ability to read protocols and SAPs and translate clinical intent into implementable data specifications
  • Excellent documentation habits — mapping specs, data dictionaries, and change logs that satisfy sponsor audit expectations
  • Eligible to work in the United States
Nice to have
  • Experience with OMOP CDM, FHIR resources, or real‑world data interoperability projects
  • Exposure to NexaSource, custom eSource platforms, or site‑centric capture workflows
  • Knowledge of ICH E6(R2) GCP requirements for data integrity and ALCOA+ principles
  • Python or similar scripting for mapping validation, diff analysis, or automated spec generation
  • Prior work with CROs, mid‑size sponsors, or multi‑site network rollouts
  • Familiarity with AI‑assisted mapping or clinical NLP for document extraction
What we offer

Join a clinical technology company where data architecture decisions ship to production on live studies — not sit in enterprise backlog limbo. You will shape the foundation that Nexa Bus, NexaSource, and our QC operations depend on.

  • Competitive salary, equity consideration, and comprehensive US health benefits
  • Hybrid or remote flexibility anchored to our Austin headquarters
  • Direct influence on product data models and integration strategy
  • Collaboration with engineering teams in Lahore and QC operations in Dubai
  • Conference and certification support for CDISC, FHIR, and clinical data management credentials
  • Clear path to lead architect or Head of Data & Integrations as the portfolio grows
Location

Austin, Texas, United States Region: North America Country: United States City: Austin, TX Hybrid / remote within US time zones — periodic presence at Austin HQ

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