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Clinical Database Programmer Jobs in New Jersey (NOW HIRING)

CYNET SYSTEMS

Azure DB Developer

Montvale, NJ · On-site

$55 - $60/hr

Experience with Azure hosted databases and cloud-based architectures. * Hands on experience with ... We deliver agile, scalable talent solutions across IT, engineering, life sciences, clinical, and ...

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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 Sep 3, 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:

Clinical Database Programmer jobs near you
Infographic showing various Clinical Database Programmer job openings in New Jersey as of August 2026, with employment types broken down into 87% Full Time, and 13% Contract. Highlights an 100% In-person job distribution, with an average salary of $120,774 per year, or $58.1 per hour.

Clinical SAS Programmer

Katalyst Healthcares & Life Sciences

Newark, NJ • On-site

Contractor

Re-posted 16 days ago

Job description

Company Description
  • Katalyst Healthcares & Life Sciences is hiring entry level candidates for several positions for contract research in Clinical trials of drugs, biologics and medical devices.
  • We have a few immediate job opportunities available in Drug Safety and Pharmacovigilance and Clinical Research field. We work with University hospitals, pharmaceutical companies and recruiting partners.
Job Description

Responsibilities:

  • Effectively designs and codes SAS programs using BASE/SAS, SAS/STAT, SAS/GRAPH and SAS MACROS for assigned clinical projects(s).
  • Produces and delivers CDISC and regulatory compliant SDTM, and ADaM standard datasets.
  • Creates and validates tables, figures and listings (TFLs) in a timely and high-quality fashion, consistently meeting objectives of the study, and regulatory requirements.
  • Provides input in the design and development of case report forms and clinical databases.
  • Performs quality control checks/validation of SAS code and output produced by other Statistical Programmers for SDTM datasets, ADaM datasets and TFLs.
  • Programs for quality checks for clinical study raw data and report the findings to Data Management.
  • Provides input in the design and development of case report forms and clinical study databases.
  • Reviews or author aCRF, SDTM and ADaM datasets specifications for datasets programming.

Requirements:

  • MS in Statistics, Computer Science, or a related field with at least 3 years or BS in Statistics, Computer Science, or a related field with at least 5 years.
  • Experience in providing statistical programming support to early and late phase clinical trials.
  • Excellent skills in SAS programming and statistical reporting.
  • Knowledge of CDISC standards for SDTM and ADaM and FDA electronic data submission requirements.
  • Familiarity with FDA and ICH regulations and guidelines.
  • Excellent problem-solving skills.
  • Good written and verbal communication skills and organizational and documentation skills.
  • Ability to work on a multidisciplinary team that may include Biostatistics, Medical Directors, Data Management, Medical Writing, Pharmacovigilance, Clinical Operations, Medical Affairs, etc.
  • Ability to prioritize and multi-task effectively.
  • Demonstrated positive attitude and the ability to work well with others.
Additional Information

All your information will be kept confidential according to EEO guidelines.

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About Katalyst Healthcares & Life Sciences

Sourced by ZipRecruiter

Katalyst HealthCares & Life Sciences is a Global Contract Research Organization that provides services in Clinical Research, Manufacturing & Quaity, Regulatory Affairs Areas.. Industries Serving: Pharmaceutical Bio-Pharmaceutical Medical Device Cosmeceuticals & Cosmetics Food & Beverage Clinical Research Scientific Areas Covering: Clinical Research Manufacturing Quality & Validations Regulatory Affairs Intellectual Property Through our in-house team expertise, associates and alliances in the US, Europe and Asia, we can rapidly deliver services, technology, processes and workforce globally, either virtually or integrate into client project space, providing oversight and expertise for individual needs to total end-to-end support for all kinds of clinical trials of Pharma, Biotech, Medical Device and all other scientific products and their manufacturing.

Industry

Scientific research and development services

Company size

51 - 200 Employees

Headquarters location

South Plainfield, NJ, US

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