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Cdx Jobs in Texas (NOW HIRING)

TIBCO Middleware Administrator

Irving, TX · On-site

$50.50 - $66.25/hr

Support messaging integration for Tibco only As a Service monitoring observability CDX and other supported platforms * Cover onboarding monitoring incident and change support resiliency reporting and ...

Cdx information

See Texas salary details

$14

$30

$36

How much do cdx jobs pay per hour?

As of Aug 26, 2026, the average hourly pay for cdx in Texas is $30.26, according to ZipRecruiter salary data. Most workers in this role earn between $30.00 and $35.72 per hour, depending on experience, location, and employer.

What is a CDX?

CDX typically stands for 'Clinical Data Exchange' professionals. These individuals are responsible for managing, integrating, and facilitating the secure sharing of clinical data between healthcare organizations, providers, and systems. Their work ensures that patient data is accessible, accurate, and compliant with healthcare regulations such as HIPAA. CDX professionals often work with electronic health records (EHRs), interoperability standards, and data security protocols to improve patient care and operational efficiency.

What are the key skills and qualifications needed to thrive as a CDX?

To thrive as a Clinical Documentation Expert (CDX), you need a solid background in medical terminology, clinical coding, and healthcare documentation, often supported by credentials such as RHIA, RHIT, or CCDS. Familiarity with electronic health record (EHR) systems, clinical coding software, and regulatory compliance tools is typically required. Strong attention to detail, critical thinking, and effective communication skills help ensure accurate and thorough documentation. These skills are crucial for maintaining healthcare quality, supporting reimbursement, and ensuring regulatory compliance.

How does a Clinical Data Exchange specialist typically collaborate with other healthcare professionals and IT teams?

A Clinical Data Exchange (CDX) specialist works closely with healthcare providers, IT staff, and data analysts to ensure secure and efficient transfer of patient information between different electronic health record (EHR) systems. Collaboration often involves participating in cross-functional meetings to address data integration challenges, clarify technical requirements, and troubleshoot interoperability issues. CDX specialists also provide training or support to end-users and help maintain compliance with healthcare data privacy regulations. This teamwork is essential to ensure that patient information flows seamlessly and securely across various healthcare platforms.

What is the difference between Cdx vs Data Analyst?

AspectCdxData Analyst
Required CredentialsCertification in CDX software, technical skillsBachelor's in Data Science, Statistics, or related field
Work EnvironmentConstruction, engineering, or infrastructure projectsBusiness, finance, healthcare, or marketing sectors
Employer & Industry UsageUsed by construction firms, engineering companiesUsed across various industries for data interpretation
Common Search & ComparisonYesYes

The main difference between Cdx and Data Analyst lies in their focus and industry application. Cdx specializes in construction and engineering data management, requiring specific certifications and software skills. Data Analysts work across multiple industries analyzing data to inform business decisions, often with a broader educational background. Both roles involve data handling but serve different sectors and purposes.

Infographic showing various Cdx job openings in Texas as of August 2026, with employment types broken down into 100% Full Time. Highlights an 88% In-person, 6% Hybrid, and 6% Remote job distribution, with an average salary of $62,933 per year, or $30.3 per hour.

Staff Program Manager, CDx

Austin, TX • On-site


Thermo Fisher Scientific
Biotechnology Research and Development • 10K+ employees

7.8

Company rating: 7.8 out of 10

Based on 428 frontline employees who took The Breakroom Quiz

174th of 544 rated manufacturers

People enjoy working here

Good employer

Recommended by students


$113K - $151K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

This job post has expired today. Applications are no longer accepted.


Job description

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Office

Job Description

As part of the Thermo Fisher Scientific team, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier, cleaner and safer. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the world’s toughest challenges, like protecting the environment, making sure our food is safe or helping find cures for cancer.

Location/Division-Specific Information:

Site-based. Relocation assistance is NOT provided. 

*Must be legally authorized to work in the United States without sponsorship.

*Must be able to pass a comprehensive background check, which includes a drug screen.

Discover Impactful Work:

As Staff Program Manager, you will own the development, external relationships, financial model, and regulatory submission of Next Generation Sequencing (NGS) based Oncology Companion Diagnostic (CDx) assays within the Clinical Sequencing Division.As Staff Program Manager you will own the development, external relationship, financial model, and regulatory submission of Next Generation Sequencing (NGS) based Oncology Companion Diagnostic (CDx) assays within the Clinical Sequencing Division. You will complete program goals from initial concept and deal agreement through successful commercialization in coordination with external clients.

  • Serve as Core Team Lead and external point of contact for multiple CDx programs.
  • Proactively identify risks and mitigations: Develop plans to address, facilitate tradeoff decisions at the portfolio level, raise to key internal partners, remove obstacles, and seek resolution.
  • Develop and control program timelines in conjunction with both internal functions and external clients.
  • Build and control budgets with Finance and external partners.
  • Conduct internal and external team meetings: Ensure decisions are made with data, supervise progress, identify & implement risk mitigations, and action items are completed to support successful program execution.
  • Present and communicate to senior leadership routinely during Product Approval Committee (PAC) meetings and additional PMO operating mechanisms.
  • Ensure compliance to company Product Commercialization Process (PCP) and Quality Management Systems (QMS) for developing regulated products.

Keys to Success:

Education and Experience

  • BS in Molecular Biology, Genetics, or Engineering required.
  • Certified Project Management Professional (PMP) preferred.
  • 7+ years of program management experience including principles, tools, and applications (i.e., timeline management, prioritization, cost estimation, risk analysis, and core team leadership).
  • Led multiple product development programs with an external partner to completion.
  • Experience with regulated medical devices developed under 21 CFR Part 820 Subpart C - Design Controls (or other regulated product development such as drugs or biologics).
  • Proficiency with Project Management software to lead intricate program timelines and resources.
  • Outstanding written and verbal presentation skills: Assertively and effectively articulates sophisticated concepts and ideas to broad audiences.
  • Confidence interacting with all levels of management, stays focused and on-point, and is able to raise problems or challenges in a productive manner.
  • Financial competence: Leads all aspects of program budgets, revenue modeling, and is comfortable reporting into Profit & Loss (P&L) statements monthly.
  • Outstanding influencing skills: Gets things done and drives decisions without formal authority.
  • Strong interpersonal skills: Nurtures relationships across the matrixed organization to resolve discord thoughtfully.

Benefits:

We offer competitive remuneration, annual incentive plan bonus, healthcare, and a range of employee benefits. Thermo Fisher Scientific offers employment with an innovative, forward-thinking organization, and outstanding career and development prospects. We offer an exciting company culture that stands for integrity, intensity, involvement, and innovation!

Compensation and Benefits

The salary range estimated for this position based in California is $113,500.00–$151,300.00.

This position may also be eligible to receive a variable annual bonus based on company, team, and/or individual performance results in accordance with company policy. We offer a comprehensive Total Rewards package that our U.S. colleagues and their families can count on, which includes:

  • A choice of national medical and dental plans, and a national vision plan, including health incentive programs

  • Employee assistance and family support programs, including commuter benefits and tuition reimbursement

  • At least 120 hours paid time off (PTO), 10 paid holidays annually, paid parental leave (3 weeks for bonding and 8 weeks for caregiver leave), accident and life insurance, and short- and long-term disability in accordance with company policy

  • Retirement and savings programs, such as our competitive 401(k) U.S. retirement savings plan

  • Employees’ Stock Purchase Plan (ESPP) offers eligible colleagues the opportunity to purchase company stock at a discount

For more information on our benefits, please visit: https://jobs.thermofisher.com/global/en/total-rewards



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