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Clinical Database Programmer Jobs in New Jersey (NOW HIRING)

Senior Statistical Programmer

Rahway, NJ ยท On-site

$117 - $184.20/hr

Clinical Database Programming * Clinical Trials * Collaborative Development * Data Modeling * Pharmaceutical Development * Project Leadership * Stakeholder Relationship Management * Statistical ...

Clinical Database Programming, Clinical Trials, Collaborative Development, Data Modeling, Pharmaceutical Development, Project Leadership, Stakeholder Relationship Management, Statistical Programming ...

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Clinical Database Programmer information

See New Jersey salary details

$70.6K

$120.8K

$215.2K

How much do clinical database programmer jobs pay per year?

As of Aug 24, 2026, the average yearly pay for clinical database programmer in New Jersey is $120,774.00, according to ZipRecruiter salary data. Most workers in this role earn between $81,200.00 and $182,700.00 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 New Jersey?

The most popular types of Clinical Database Programmer jobs in New Jersey are:

What are popular job titles related to Clinical Database Programmer jobs in New Jersey?

For Clinical Database Programmer jobs in New Jersey, the most frequently searched job titles are:

What job categories do people searching Clinical Database Programmer jobs in New Jersey look for?

The top searched job categories for Clinical Database Programmer jobs in New Jersey are:

What are popular job titles related to Clinical Database Programmer jobs in NJ?

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

Infographic showing various Clinical Database Programmer job openings in New Jersey as of August 2026, with employment types broken down into 90% Full Time, and 10% Contract. Highlights an 100% In-person job distribution, with an average salary of $120,774 per year, or $58.1 per hour.

Senior Specialist, Clinical Data Management

Jobtailor

Rahway, NJ โ€ข On-site

$90 - $150/hr

Other

Posted 6 days ago


Job description

  • Oversees and coordinates clinical database activities for multiple clinical programs.
  • Interface with CDS manager/supervisor to assure consistency of technical and process strategies.
  • Acts as a technical resource to other members of the group.
  • Plans appropriately to ensure adherence to timelines.
  • Interface with members of study teams, including external CROs/Vendors where applicable, to integrate study team requirements into all deliverables.
  • Creates and develops clinical databases and data transfer files according to written specifications.
  • Ensures adherence to clinical database standards, SOPs and Process Guidelines.
  • Leads and participates in the review of eCRFs and edit checks, database development, programming of edit checks, and scripts to aid in transfer of electronic data files into the Clinical Data Management System (CDMS).
  • Trains new hires and participates in the interview process.
  • Provide ongoing training and development to Clinical Database Developers on existing standards.
  • Helps to develop a customer oriented and can-do attitude in the group and contributes as subject matter expert for trouble-shooting findings.
  • Leads and participates in extra activities including, but not limited to, task forces, testing of new systems and helps coordinate CDS technical initiatives.
  • Contributes strategies, innovative and creative solutions to enhance processes and increase productivity of the group.
  • Provides ongoing clinical database support to other departments.
  • Assist clinical database manager/supervisor in project planning, manpower projections and resource allocations across therapy areas.
Requirements
  • 4 years of database development or data cleaning programming experience, at least 3 of which including clinical databases and programming.
  • Demonstrated strong technical proficiency in a Clinical Data Management System. Particularly Veeva EDC, Central Designer, SQL-PL/SQL.
  • At least 4 yearsโ€™ experience with Oracle databases and SQL.
  • Solid knowledge of MS Windows/Office software and exposure to web-based applications.
  • Ability to establish and maintain good working relationships with different functional areas.
  • Strong sense of urgency and customer focus.
  • Project Management skills
  • Ability to present in a group environment
  • Leadership, verbal and written communication, interpersonal and organizational skills
  • Desire and ability to learn new processes and technologies
  • Broad knowledge of Clinical Development and Regulatory Affairs requirements
  • Ability to multi-task, work independently, and good communication skills
  • Understanding of drug discovery process, FDA regulations, GxP guidelines, ICH guidelines, clinical database cleaning process, and 21 CFR Part 11.
Core Competencies

Demonstrates expertise in Clinical Database Development and Management, with strong technical proficiency in Veeva EDC, SQL, and Oracle databases. Capable of leading teams, ensuring adherence to clinical standards, and fostering effective communication across functional areas.

Highest-signal resume keywords
  • Clinical Database Development
  • Veeva EDC
  • SQL-PL/SQL
  • Project Management
  • Clinical Data Management System
ATS Optimization Keywords Hard Skills
  • Database Development
  • Data Cleaning Programming
  • Oracle Databases
  • Clinical Database Standards
  • ECRF Review
  • Edit Check Programming
  • Data Transfer Files
  • Clinical Database Support
  • Regulatory Affairs Knowledge
  • GxP Guidelines
Soft Skills
  • Leadership
  • Communication Skills
  • Interpersonal SkillsOrganizational Skills
  • Customer Focus
Industry Keywords
  • Clinical Development
  • FDA Regulations
  • ICH Guidelines
  • Drug Discovery Process
  • 21 CFR Part 11
Tools & Technologies
  • MS Windows
  • MS Office
  • Web-Based Applications
  • Clinical Data Management System
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