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Clinical Database Programmer Jobs (NOW HIRING)

Senior Clinical Database Programmer The Senior Clinical Database Programmer will work under the supervision of Principal CDP (or higher-level role) but may work independently as project lead. Working ...

The eClinical / Medidata Database Programmer is responsible for building, configuring, testing, and maintaining clinical study databases and related eClinical system components. This role supports ...

We are looking for a performance-oriented, innovative and self-motivated team player to join our Clinical Data Sciences team as a full-time Electronic Data Capture (EDC) Database Developer / Clinical ...

We are looking for a performance-oriented, innovative and self-motivated team player to join our Clinical Data Sciences team as a full-time Electronic Data Capture (EDC) Database Developer / Clinical ...

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 ...

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 ...

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 ...

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Clinical Database Programmer information

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$69.5K

$119K

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How much do clinical database programmer jobs pay per year?

As of Jul 21, 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.

More about Clinical Database Programmer jobs
What cities are hiring for Clinical Database Programmer jobs? Cities with the most Clinical Database Programmer job openings:
What are the most commonly searched types of Clinical Database Programmer jobs? The most popular types of Clinical Database Programmer jobs are:
Who are the top companies hiring for Clinical Database Programmer jobs? The top employers for Clinical Database Programmer jobs are:
What states have the most Clinical Database Programmer jobs? States with the most job openings for Clinical Database Programmer jobs include:
Infographic showing various Clinical Database Programmer job openings in the United States as of July 2026, with employment types broken down into 85% Full Time, 6% Part Time, 6% Contract, and 3% Summer. Highlights an 76% In-person, and 24% Remote job distribution, with an average salary of $118,962 per year, or $57.2 per hour.
Senior Clinical Database Programmer

Senior Clinical Database Programmer

Veristat

Remote

Full-time

Medical, Retirement

Re-posted 5 days ago


Job description

Job Description:

Senior Clinical Database Programmer

The Senior Clinical Database Programmer will work under the supervision of Principal CDP (or higher-level role) but may work independently as project lead. Working closely with members of Data Management, Statistics, Information Technology (IT), and Quality Control (QC) Departments, the Senior Clinical Database Programmer is responsible for the design and development of electronic and paper Case Report Forms, and to manage, direct, and enable set up of studies using Company's clinical data management systems, including the maintenance and development of computer programs and processes that support team's activities, within scope, budget and timelines in compliance with the United Kingdom Statutory Instrument 2004 No. 1031 and its subsequent amendments, ICH guidelines for Good Clinical Practice and other national and international standards and legislation (as required), Company procedures, and client instructions.

Make an Impact at Veristat!

Join a global team with more than 30 years of expertise accelerating life-changing therapies to patients worldwide.

  • 105+ approved therapies for marketing applications prepared by Veristat
  • 480+ oncology projects in the past 5 years
  • 350+ rare disease projects delivered in the past 5 years
  • Flexible, inclusive culture - 70% remote workforce, 66% women-led teams

Learn more about our core values here!

What we offer

  • The estimated hiring range for this role is $104K to $115K USD plus applicable bonus. This hiring range is specific to the US and will vary for other regions based upon local market data. Final salary is ultimately decided upon taking into account a wide range of factors, including but not limited to skills and experience, licensure and certifications, education, specific location and dynamic market data.
  • Benefits vary by location and may include:
    • Remote working
    • Flexible time off
    • Paid holidays
    • Medical insurance
    • Tuition reimbursement
    • Retirement plans

What we look for

Bachelor's degree or equivalent (preferred in science) or equivalent work experience.

5-7 years industry and sector experience in eCRF design and development with commercially available CDMS- i.e., Medidata Rave, Oracle InForm/ Central Designer, Veeva, DataLabs, Medrio.

4 years' experience leading eCRF Design/Development/ Maintenance projects and activities without support of a senior colleague.

Able to lead complex studies.

Automated Decision Making: All applicants are reviewed by a member of the Veristat Talent Acquisition team; Veristat does not utilize an automated decision-making process.

Veristat is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees.