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Clinical Database Programmer Jobs (NOW HIRING)

Allucent

Senior Clinical Programmer I

In this role, you'll play a key part in building and maintaining clinical databases, leading programming activities across global studies, and collaborating with cross-functional teams to deliver ...

CTI

Clinical Programmer

Covington, KY · On-site +1

Act as a primary database architect for client clinical databases using Medidata Rave, OmniComm TrialMaster, or other database applications as needed for Clinical Trials * Create database entry ...

CTI

Clinical Programmer

Covington, KY · On-site +1

Act as a primary database architect for client clinical databases using Medidata Rave, OmniComm TrialMaster, or other database applications as needed for Clinical Trials * Create database entry ...

Atorus Research

Sr Medidata RAVE Programmer

S. or Canada Contract/Corp to Corp JOB OVERVIEW The Electronic Data Capture (EDC) Programmer is responsible for providing support in creating, deploying and maintaining clinical databases and ...

Collabera

Clinical Data Manager

Irvine, CA · On-site

Work closely with clinical project team and database programmers to provide edit check requirements and specifications at the time of study database development and Post production changes. Ensure ...

Systimmune

Clinical Data Manager

Redmond, WA · On-site

$100K - $170K/yr

The CDM will support and/or lead clinical database design, data collection and validation, data ... Biostatisticians, Statistical Programmers, Medical Monitors, Clinical Scientists, Clinical Project ...

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Samprasoft

SQL Database Developer/Engineer

Oakland, CA · On-site

Senior Database Developer/Engineer Digital Intelligence Solutions (DISYS) is seeking a Senior Database Developer/Engineer to provide Clinical Data solutions for Health Care informatics efforts as ...

SystImmune, Inc

Clinical Data Manager

Redmond, WA · On-site

$100K - $170K/yr

The CDM will support and/or lead clinical database design, data collection and validation, data ... Biostatisticians, Statistical Programmers, Medical Monitors, Clinical Scientists, Clinical Project ...

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Clinical Database Programmer information

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How much do clinical database programmer jobs pay per year?

As of Jun 30, 2026, the average yearly pay for clinical database programmer in the United States is $118,962.00, according to ZipRecruiter salary data. Most workers in this role earn between $80,000.00 and $180,000.00 per year, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive in the Clinical Database Programmer position, and why are they important?

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 is a Clinical Database Programmer job?

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 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.

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Clinical Database Programmer jobs near you
Infographic showing various Clinical Database Programmer job openings in the United States as of June 2026, with employment types broken down into 6% As Needed, 3% Full Time, 61% Part Time, and 30% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $118,962 per year, or $57.2 per hour.
Senior Clinical Programmer I

Senior Clinical Programmer I

Allucent

Remote

Full-time

Posted 4 days ago

Job description

At Allucent™, we are dedicated to helping small-medium biopharmaceutical companies efficiently navigate the complex world of clinical trials to bring life-changing therapies to patients in need across the globe.
We're looking for a Senior Clinical Programmer I who thrives on solving complex challenges and transforming clinical data into high-quality, reliable insights that drive drug development. In this role, you'll play a key part in building and maintaining clinical databases, leading programming activities across global studies, and collaborating with cross-functional teams to deliver data that accelerates better outcomes for patients. Beyond study execution, you'll have the opportunity to influence departmental processes, mentor colleagues, and help shape the future of clinical programming within a collaborative and innovation-driven environment.
About the RoleAs a Senior Clinical Programmer I, you will lead clinical programming activities that support the successful delivery of global clinical studies, ensuring high-quality data capture, database development, and regulatory compliance throughout the study lifecycle. You'll collaborate cross-functionally to design, build, validate, and maintain clinical databases, develop programming solutions and data visualizations, and champion CDISC standards and programming best practices. In addition to managing project timelines, budgets, and deliverables, you'll drive process improvements, contribute to business development activities, and provide technical leadership and mentorship to junior team members.
Your main responsibilities will include but not limited to:
  • Lead clinical programming activities across assigned studies, ensuring project timelines, budgets, deliverables, and resource needs are effectively managed while proactively identifying and escalating risks or change orders.
  • Design, build, validate, and maintain clinical databases, electronic edit checks, data listings, and data visualization tools to support high-quality data collection, review, and regulatory compliance.
  • Collaborate cross-functionally with Data Management, Project Management, Biostatistics, and study teams to develop study documentation, clarify technical specifications, and deliver programming solutions that meet project objectives.
  • Champion industry standards and quality, applying CDISC conventions (CDASH, SDTM, TAUGs), validation principles, and programming best practices to ensure consistent, compliant, and inspection-ready deliverables.
  • Drive innovation and continuous improvement by leading process enhancements, developing global programming standards and libraries, implementing data analytics and visualization tools, and supporting departmental initiatives.

Requirements
About You
If you are a collaborative and detail-oriented clinical programming professional who enjoys solving complex technical challenges and takes pride in delivering high-quality, compliant data solutions that support global clinical trials. This role will give you the opportunity to combine strong expertise in clinical database programming, CDISC standards, and cross-functional collaboration with a passion for continuous improvement, mentoring others, and driving innovation in clinical data management.
To be successful we are looking for the following traits and behaviors:
  • Life science, healthcare, Computer Science and/or related field degree
  • Minimum 5 years of experience in drug development and/or clinical research
  • Good understanding and hands-on experiences of CDISC standards (i.e. CDASH, TAUGs and SDTM models)
  • Expert with electronic data capture (EDC) software systems and other tools for managing clinical studies
  • Expert in technical data management practices (developing programs, validation plans, testing, and documentation)

About Allucent
Our mission is to help bring new therapies to light. When you work at Allucent, that means rolling up your sleeves and applying your unique skill set, expertise, and knowledge to build partnerships with our clients in their pursuit to develop new, life-improving treatments.
If you're passionate about helping customers develop new pharmaceuticals and biologics; have an entrepreneurial spirit; and ready to join other science, business, and operations leaders, we would love to get to learn more about how we can help each other grow.
Together we SHINE. Find more information about our values.
Benefits
Benefits of working at Allucent include:
  • Comprehensive benefits package per location
  • Competitive salaries per location
  • Departmental Study/Training Budget for furthering professional development
  • Flexible Working hours (within reason)
  • Opportunity for remote/hybrid* working depending on location
  • Leadership and mentoring opportunities
  • Participation in our enriching Buddy Program as a new or existing employee
  • Internal growth opportunities and career progression
  • Financially rewarding internal employee referral program
  • Access to online soft-skills and technical training via internal platforms
  • Eligibility for our Spot Bonus Award Program in recognition of going above and beyond on projects
  • Eligibility for our Loyalty Award Program in recognition of loyalty and commitment of longstanding employees

Apply now!
If you are interested in this role please apply through the button or for more information reach out to Demetria Eggleston at Demetria.eggleston@allucent.com
Disclaimers:
*Our policy encourages a dynamic work environment, prescribing a minimum of 2 days in office per week for employees within a reasonable distance from one of our global offices.
"The Allucent Talent Acquisition team manages the recruitment and employment process for Allucent (US) LLC and its affiliates (collectively "Allucent"). Allucent does not accept unsolicited resumes from third-party recruiters or uninvited requests for collaboration on any of our open roles. Unsolicited resumes sent to Allucent employees will not obligate Allucent to the future employment of those individuals or potential remuneration to any third-party recruitment agency. Candidates should never be submitted directly to our hiring managers, employees, or human resources."
#LI-DH-1 #LI-Remote #LI-Hybrid

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