ZipRecruiter

Log In

1

Clinical Database Programmer Jobs in Austin, TX (NOW HIRING)

DiaSorin

Clinical Data Scientist

Austin, TX · On-site

Ensure the overall accuracy and integrity of the Clinical Affairs study databases. * Implementing ... database troubleshooting. * Manage the development of primary and validation programming and lead ...

DiaSorin

Clinical Data Scientist

Austin, TX

Ensure the overall accuracy and integrity of the Clinical Affairs study databases. * Implementing ... database troubleshooting. * Manage the development of primary and validation programming and lead ...

Medclinicx

Technical Architect

Austin, TX · On-site

$140 - $210/hr

Evaluate tooling and build proof-of-concepts for engineers. * Architect secure workflows for clinical databases and portals. * Configure database logical scaling and Row-Level Security (RLS)

Hirekeyz Inc

Developer/Programmer Analyst

Austin, TX · On-site

... clinical research trial results, statistical study of traffic patterns, or analyzing and developing ... other databases as the backend data storage model 2 Preferred Communication, analytical and ...

Medclinicx

ERP Developer

Austin, TX · On-site

$110 - $150/hr

Optimize database queries and interface speed. * Integrate ERP packages with central cloud ... Build automation for clinical and administrative workflows * Work with SaaS, backend, and ...

New

Medclinicx

Backend Engineer

Austin, TX · On-site

$120 - $180/hr

Implement database schemas and data models. * Work with distributed systems and cloud ... Work on real clinical and operational data systems * Collaborate with AI, cloud, and product teams

New

Career Opportunities

Data Engineer

Austin, TX · On-site

$113K - $136K/yr

ABOUT TRUDATARX TruDataRx, Inc. uses objective clinical data to help clients improve the clinical ... Experience with database management * Experience handling healthcare data formats (e.g. Pharmacy ...

Medclinicx

Application Architect

Austin, TX · On-site

$140 - $190/hr

... engineering leads on architecture decisions. * Review code structures, patterns, and database ... Clinical Workflow Applications Architect automation pipelines, clinical routing schedulers, and ...

New

Medclinicx

Business Intelligence Developer

Austin, TX · On-site

$90 - $120/hr

Develop reports for clinical, operational, and business insights. * Transform raw healthcare data ... Understanding of relational database modeling principles. Preferred * Experience in US healthcare ...

New

CYNET SYSTEMS

Senior Rust Developer

Round Rock, TX · On-site

$47 - $52/hr

Integrate applications with cloud platforms, databases, messaging systems, and enterprise platforms ... We deliver agile, scalable talent solutions across IT, engineering, life sciences, clinical, and ...

Natera

Senior Lab Automation Engineer

Austin, TX · On-site

$103K - $135K/yr

Background in NGS laboratories is a plus, as is background in clinical laboratories. * Experience in software programming and data handling (including database work) is a plus. * Strong attention to ...

LivaNova

Regulatory & Clinical Specialist

Austin, TX · Remote

$85K - $95K/yr

... databases. * Demonstrated experience in the development, writing and editing of regulatory ... Minimum of a master's degree in biomedical engineering, science or equivalent technical discipline ...

PICTOR LABS INC

Senior Software Engineer

Austin, TX · On-site

$118K - $156K/yr

This innovation supports the critical evolution from research applications to clinical deployment ... Design and implement efficient database schemas for cloud service management, edge device ...

next page

Showing results 1-20

All JobsClinical Database Programmer JobsClinical Database Programmer Jobs in Austin, TX

Clinical Database Programmer information

See Austin, TX salary details

$68.9K

$117.9K

$210.1K

How much do clinical database programmer jobs pay per year?

As of Aug 21, 2026, the average yearly pay for clinical database programmer in Austin, TX is $117,916.00, according to ZipRecruiter salary data. Most workers in this role earn between $79,300.00 and $178,400.00 per year, depending on experience, location, and employer.

What is a clinical database programmer?

A Clinical Database Programmer is responsible for designing, developing, and maintaining databases used in clinical trials. They ensure that data is collected, stored, and managed efficiently while complying with regulatory standards such as CDISC and FDA guidelines. Their role involves creating database structures, writing validation checks, and supporting data analysis to ensure accurate and reliable clinical trial results. They often work with clinical data managers, biostatisticians, and regulatory teams.

What are the key skills and qualifications needed to thrive as a clinical database programmer?

To excel as a Clinical Database Programmer, you need a bachelor's degree in computer science or a related field, experience in database design, and a strong understanding of clinical data standards. Proficiency in database management systems (such as Oracle or SQL), knowledge of electronic data capture (EDC) tools like Medidata Rave, and familiarity with programming languages like SAS or SQL are commonly required, along with certifications such as CDISC or Medidata Solutions. Attention to detail, problem-solving ability, and strong communication skills are valuable soft skills for this role. Mastering these competencies is vital for ensuring high-quality, regulatory-compliant clinical trial data and effective collaboration within multidisciplinary research teams.

What are common responsibilities and team interactions for a clinical database programmer in a typical workweek?

As a Clinical Database Programmer, your primary responsibilities usually include designing, building, and validating clinical trial databases, ensuring data is collected and managed in compliance with industry standards and regulatory requirements. You will frequently collaborate with clinical data managers, biostatisticians, and study coordinators to define data collection requirements and resolve data discrepancies. Team meetings and cross-functional communication are integral parts of the role, as you work together to maintain database integrity throughout the study lifecycle. This collaborative environment provides valuable experience in both technical problem-solving and teamwork, often paving the way for advancement into senior programming or data management positions.

What are the most commonly searched types of Clinical Database Programmer jobs in Austin, TX?

The most popular types of Clinical Database Programmer jobs in Austin, TX are:

What are popular job titles related to Clinical Database Programmer jobs in Austin, TX?

For Clinical Database Programmer jobs in Austin, TX, the most frequently searched job titles are:

What job categories do people searching Clinical Database Programmer jobs in Austin, TX look for?

The top searched job categories for Clinical Database Programmer jobs in Austin, TX are:

What cities near Austin, TX are hiring for Clinical Database Programmer jobs?

Cities near Austin, TX with the most Clinical Database Programmer job openings:

Clinical Database Programmer jobs near you
Infographic showing various Clinical Database Programmer job openings in Austin, TX as of August 2026, with employment types broken down into 3% As Needed, 73% Full Time, 16% Part Time, and 8% Contract. Highlights an 94% Physical, 1% Hybrid, and 5% Remote job distribution, with an average salary of $117,916 per year, or $56.7 per hour.

Clinical Data Scientist

DiaSorin

Austin, TX • On-site

Full-time

Re-posted 13 days ago

DiaSorin rating

7.7

Company rating: 7.7 out of 10

Based on 11 frontline employees who took The Breakroom Quiz

Job description

Obsessed by Science. Entrepreneurial by Nature. United by Purpose.
Diasorin is a global leader in immunodiagnostic and molecular diagnostic solutions, advancing science to improve patient outcomes worldwide. For more than 50 years, we have combined scientific rigor with an entrepreneurial mindset, operating with a strong commitment to innovation, accountability, and results to deliver trusted diagnostic solutions.
As the Diagnostics Specialist, Diasorin continuously invests in research, technology, and people. Guided by our values of operational excellence, customer focus, and teamwork, we empower teams to think boldly, act decisively, and transform ideas into meaningful impact across one of the industry's broadest specialty diagnostic portfolios.
When you join Diasorin, you are not just filling a role. You are helping build what comes next.
Why Join Diasorin
  • Build What Matters
    Take ownership, challenge the status quo, and contribute directly to solutions that improve patient care worldwide.
  • Innovate with Agility at a Global Scale
    Work in an entrepreneurial environment that enables speed, collaboration, and global impact.
  • Grow in a People-Centered Culture
    Thrive in a culture that values accountability, inclusion, and continuous development.

Job Scope
This position plays an integral role in the development, sourcing and maintenance of clinical data management tools, database, and software for in vitro diagnostic products. The role involves activities related to ensuring the overall accuracy and integrity of clinical studies data in accordance with applicable global regulations and standards (e.g. 21 CFR Part 812, CLSI, ICH) that demonstrate the performance and utility of in vitro diagnostic products.
Key Duties and Responsibilities
  • Ensure the overall accuracy and integrity of the Clinical Affairs study databases.
  • Implementing administrative procedures and policies to support database system use.
  • Maintaining user access to the system and providing initial database training for new users.
  • Entering new studies into the database and validating new study databases before clinical inputs are performed.
  • Leading database users in preparing reports, tabulations, CRF preparation and database troubleshooting.
  • Manage the development of primary and validation programming and lead the report generation activity for clinical trials.
  • Possessing knowledge of domestic and international clinical requirements including GCP and is able to perform these essential duties and responsibilities with some direct supervision.
  • Working closely with external Data Management contractors, Clinical Development, Clinical Affairs, the Clinical Trial Managers, Sample Bank team, Legal department, Logistics team, and Marketing teams to ensure project tasks are managed to completion.
  • Ensure standards for statistical analyses are followed via statistical program validation and quality control activities.
  • Provide statistical input, develop statistical analysis plan for clinical study protocols.
  • Manage data management project timelines and schedules for projects within and outside the department.
  • Select, validate, manage database for clinical data tracking (EDC system)
  • Responsible for monitoring assigned clinical and outcomes studies to ensure compliance with clinical study protocols, investigator agreements, and applicable corporate regulatory requirements.
  • Other job duties as assigned, which may include:
  • Assist in developing departmental SOPs.
  • Preparation of statistical reports for regulatory submissions, including global, FDA, IRBs or internal customers
  • Preparation for departmental and executive meetings
  • Clinical data entry and QC
  • Case Report Form (CRF) and query management
  • Select, validate, manage electronic CRF (eCRF) software/database.
  • Database training for new users; support for current users
  • Sample data analysis for Product Development teams.
  • Benchmark study result analysis with Product Development and Marketing teams.
  • Carry out internal auditing of clinical databases.
  • Any other duties deemed necessary by management.

Education, Experience, and Qualifications
  • Bachelor's Degree with 5 years' in Molecular Biology / Biochemistry or related discipline, with experience in a regulated clinical research environment
  • Master's Degree with 3 years' or Ph.D. (preferred) in Molecular Biology / Biochemistry or related discipline, with experience in a regulated clinical research environment
  • Ph.D. with 1 year, in Molecular Biology / Biochemistry or related discipline, with experience in a regulated clinical research environment
  • Superior communication, presentation and writing skills.
  • Highly organized with proven time management and prioritization skills
  • Computer programing skills for clinical data mining is desired.
  • Experience in molecular and clinical data analysis.
  • Experience in searching through and understanding scientific and regulatory literature.
  • Experience in working independently in a fast-paced environment with rapidly changing priorities.
  • Experience in documentation and record management for laboratory and clinical studies (GLP and GCP)
  • Experience or knowledge of the requirements on working in a FDA regulated environment.

Travel Requirements
  • 20% 10% international

What we offer
Receive a competitive salary and benefits package as you grow your career at DiaSorin. Join our team and discover how your work can impact the lives of people all over the world.
Diasorin is committed to building a workplace where people feel empowered to contribute ideas, take ownership, and grow their careers. We believe diverse perspectives strengthen innovation and help us deliver meaningful impact for patients and customers worldwide.
Diasorin is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, protected veteran status, or any other characteristic protected by applicable law.
This posting and recruitment process are subject to applicable local laws and regulations in the country where the position is located. Additional employment disclosures, candidate rights, and employment conditions may apply based on local jurisdiction.
Individuals hired will be required to verify identity and eligibility to work and may be subject to a background check and drug screening where permitted by law. Diasorin is committed to providing reasonable accommodations for qualified individuals with disabilities during the application process. If assistance is required, please contact hr@diasorin.com.
Recruitment Fraud Notice
Diasorin never requests payment, financial information, or personal banking details from candidates at any stage of the recruitment process. Official communications from Diasorin recruiters will only come from a verified @diasorin.com email address. If you have questions about the legitimacy of a recruitment communication, please contact hr@diasorin.com for verification.
Unauthorized third-party recruiting agencies may not submit candidates for this position without prior written authorization from the Diasorin Human Resources Department.

What DiaSorin employees say

Pay

Benefits

Hours and flexibility

Workplace

Get the full story on Breakroom

Apply