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Clinical Database Programmer Jobs (NOW HIRING)

Merck & Co.

Responsibilities Oversee and coordinate clinical database activities across multiple clinical ... Adaptability, Adaptability, Artificial Intelligence (AI), Automation, Clinical Database Programming ...

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How much do clinical database programmer jobs pay per year?

As of Jun 9, 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

Clinical Database Programmer

millenniumsoft

Franklin Lakes, NJ • On-site

Contractor

Posted 19 days ago

Job description

Position: Clinical Database Programmer
Location : Franklin Lakes, NJ
Duration : 5+ Months contract
Total Hours/week: 40.00
1st Shift
Client: Medical Device Company
Employment Type: Contract on W2 (Need US Citizens Or GC Holders Only)
No H1b's
Description:
Title Contract Clinical Database Programmer 2
The Clinical Database Programmer will lead the development and maintenance of database builds in support of clinical studies. He / she will build study databases including development of database specifications/definitions, programming of CRF layouts, programming of validation and derivation procedures, and programming of various reports to support the data review process. The Clinical Database Programmer will troubleshoot technical issues as required for staff regarding specific database issues. He / She contributes to the continual process development within the data management group and helps define best practices.
Essential Job Functions:
• Develops database design specifications/definitions in consultation with data management, statistics and programming.
• Designs and creates clinical databases to enable data review/validation of the study data by Data Managers, and a comprehensive and efficient analysis by Statistics and SAS Programming.
• Programs and tests database configurations (edit checks, derivations, form/field dynamics, etc.).
• Programs and tests reports using SQL/SAS to identify inconsistencies and support data review efforts.
• Performs pre-processing and loading of non-CRF data files.
• Contributes to solutions for routine technical problems and liaises with IT as appropriate to resolve issues.
• Identify and implement solutions to data management issues and concerns that arise during the conduct of the study.
• Identifies and understands the need for standardization and takes initiative to help improve departmental efficiency.
• Establishes and maintains productive working relationships with all other functional areas that contribute to the execution of clinical studies.
• Contributes to the development of Departmental SOPs, Business Guidance and/or Standards/Templates to define best practice and promote consistency.
• Maintains all required study documentation.
Required Qualifications:
• Proficient in Oracle SQL programming
• Understanding of relational databases.
• Experience with development, validation, execution, maintenance, documentation, and archival of clinical data targeted for regulatory submission.
• Ability to work independently with minimal supervision and manage multiple deliverables concurrently.
• Ability to ensure clinical database programming work is completed in a consistent manner and validated according to department practices.
• Excellent interpersonal skills, strong written and verbal communication skills.
• Working knowledge of clinical development.
• Working understanding of clinical trial principles and technical implications.
• Ability to interact effectively within and across team environment.
• Ability to travel up to 10% of the time

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