Develop programming specifications for analysis datasets, pooled datasets and deliverables in ... clinical trials and submission activities. Working knowledge of database design/structures and ...
Develop programming specifications for analysis datasets, pooled datasets and deliverables in ... clinical trials and submission activities. Working knowledge of database design/structures and ...
Validation and quality control processes Establish efficient programming standards that ensure timely database analyses and global submission readiness. Clinical Data Management * Provide executive ...
Validation and quality control processes Establish efficient programming standards that ensure timely database analyses and global submission readiness. Clinical Data Management * Provide executive ...
Validation and quality control processes Establish efficient programming standards that ensure timely database analyses and global submission readiness. Clinical Data Management * Provide executive ...
Validation and quality control processes Establish efficient programming standards that ensure timely database analyses and global submission readiness. Clinical Data Management * Provide executive ...
Principal Data Manager I
Bridgewater, NJ · On-site +1
$130K - $165K/yr
Everest Clinical Research ("Everest") is a full-service contract research organization (CRO ... Review database edit check specifications for assigned studies. Lead efforts in developing and ...
Principal Data Manager I
Bridgewater, NJ · On-site +1
$130K - $165K/yr
Everest Clinical Research ("Everest") is a full-service contract research organization (CRO ... Review database edit check specifications for assigned studies. Lead efforts in developing and ...
Senior SAS Programmer
Woodcliff Lake, NJ · On-site
Job Title: Sr. SAS Programmer Analyst Duration: 1 year+ Location : Woodcliff Lake, NJ * Perform SAS ... clinical trials such as CDISC, SDTM, MedDRA, WHODRUG . * Good understanding of relational databases ...
Senior SAS Programmer
Woodcliff Lake, NJ · On-site
Job Title: Sr. SAS Programmer Analyst Duration: 1 year+ Location : Woodcliff Lake, NJ * Perform SAS ... clinical trials such as CDISC, SDTM, MedDRA, WHODRUG . * Good understanding of relational databases ...
Clinical Data Manager
Woodcliff Lake, NJ · On-site
Perform DM activities for in-house and outsourced trials: protocolreview, CRF development, database ... Coordinate with Programming team to provide support to the data reviewand safety updates ...
Clinical Data Manager
Woodcliff Lake, NJ · On-site
Perform DM activities for in-house and outsourced trials: protocolreview, CRF development, database ... Coordinate with Programming team to provide support to the data reviewand safety updates ...
Candidate to provide statistical programming support and validation and help set specifications of ... clinical trials and submission activities. Working knowledge of database design/structures and ...
Candidate to provide statistical programming support and validation and help set specifications of ... clinical trials and submission activities. Working knowledge of database design/structures and ...
... database lock Perform Project Management : represent DM on clinical teams, coordinate deliverables by other functions and/or CRO as necessary to achieve DM deliverables Coordinate with Programming ...
... database lock Perform Project Management : represent DM on clinical teams, coordinate deliverables by other functions and/or CRO as necessary to achieve DM deliverables Coordinate with Programming ...
clinical data manager
Jersey City, NJ · On-site
... database lock. -Perform Project Management : represent DM on clinical teams, coordinate ... with Programming team to provide support to the data review and safety updates (coordinate ...
clinical data manager
Jersey City, NJ · On-site
... database lock. -Perform Project Management : represent DM on clinical teams, coordinate ... with Programming team to provide support to the data review and safety updates (coordinate ...
Clinical Imaging Specialist
Lawrenceville, NJ · On-site
Feel free to search our database of open positions and apply for your next career move! Hundreds of ... Information Technology, Software Programmers, Engineering, Manufacturing, Legal, Plant Maintenance ...
Quick apply
Clinical Imaging Specialist
Lawrenceville, NJ · On-site
Feel free to search our database of open positions and apply for your next career move! Hundreds of ... Information Technology, Software Programmers, Engineering, Manufacturing, Legal, Plant Maintenance ...
Clinical Data Manager
Woodcliff Lake, NJ · On-site
... database lock. Perform Project Management : represent DM on clinical teams, coordinate deliverables by other functions and/or CRO as necessary to achieve DM deliverables. Coordinate with Programming ...
Clinical Data Manager
Woodcliff Lake, NJ · On-site
... database lock. Perform Project Management : represent DM on clinical teams, coordinate deliverables by other functions and/or CRO as necessary to achieve DM deliverables. Coordinate with Programming ...
Clinical Research Nurse Coordinator
Livingston, NJ · On-site
$55 - $63/hr
... trials database. * Coordinate patient reimbursement and manage oncology nursing care in ... About Actalent Actalent is a global leader in engineering and sciences services and talent ...
Clinical Research Nurse Coordinator
Livingston, NJ · On-site
$55 - $63/hr
... trials database. * Coordinate patient reimbursement and manage oncology nursing care in ... About Actalent Actalent is a global leader in engineering and sciences services and talent ...
SAS Programming
Madison, NJ · On-site
Designs and/or reviews database structure; Writes edit checks from the Data Cleaning Plan (DCP ... Acts as primary programmer to produce tables, listings, and figures for the clinical study report ...
SAS Programming
Madison, NJ · On-site
Designs and/or reviews database structure; Writes edit checks from the Data Cleaning Plan (DCP ... Acts as primary programmer to produce tables, listings, and figures for the clinical study report ...
Clinical Research Nurse
Livingston, NJ · On-site
$55 - $63/hr
... trials database. * Coordinate patient reimbursement and manage oncology nursing care in ... About Actalent Actalent is a global leader in engineering and sciences services and talent ...
Clinical Research Nurse
Livingston, NJ · On-site
$55 - $63/hr
... trials database. * Coordinate patient reimbursement and manage oncology nursing care in ... About Actalent Actalent is a global leader in engineering and sciences services and talent ...
Associate Principal Scientist, Statistical Programming
Rahway, NJ · On-site
$144K - $224K/yr
Expertise in SAS and clinical trial programming including data steps, procedures, SAS/MACRO, SAS/GRAPH; systems and database expertise. * Must possess strong familiarity with statistical analysis ...
Associate Principal Scientist, Statistical Programming
Rahway, NJ · On-site
$144K - $224K/yr
Expertise in SAS and clinical trial programming including data steps, procedures, SAS/MACRO, SAS/GRAPH; systems and database expertise. * Must possess strong familiarity with statistical analysis ...
Associate Principal Scientist, Statistical Programming
$144K - $224K/yr
Expertise in SAS and clinical trial programming including data steps, procedures, SAS/MACRO, SAS/GRAPH; systems and database expertise.Must possess strong familiarity with statistical analysis ...
Associate Principal Scientist, Statistical Programming
$144K - $224K/yr
Expertise in SAS and clinical trial programming including data steps, procedures, SAS/MACRO, SAS/GRAPH; systems and database expertise.Must possess strong familiarity with statistical analysis ...
Associate Principal Scientist, Statistical Programming
Rahway, NJ · On-site
$144K - $224K/yr
Expertise in SAS and clinical trial programming including data steps, procedures, SAS/MACRO, SAS/GRAPH; systems and database expertise. * Must possess strong familiarity with statistical analysis ...
Associate Principal Scientist, Statistical Programming
Rahway, NJ · On-site
$144K - $224K/yr
Expertise in SAS and clinical trial programming including data steps, procedures, SAS/MACRO, SAS/GRAPH; systems and database expertise. * Must possess strong familiarity with statistical analysis ...
Specialists, Clinical Data Management
Rahway, NJ · On-site
$87K - $137K/yr
Clinical Data Management, Communication, Computer Programming, Data Analysis, Data Management, Data Quality Assurance, Electronic Data Capture (EDC), PL/SQL (Programming Language), SQL Databases ...
Specialists, Clinical Data Management
Rahway, NJ · On-site
$87K - $137K/yr
Clinical Data Management, Communication, Computer Programming, Data Analysis, Data Management, Data Quality Assurance, Electronic Data Capture (EDC), PL/SQL (Programming Language), SQL Databases ...
Specialists, Clinical Data Management
Rahway, NJ · On-site
$87K - $137K/yr
Clinical Data Management, Communication, Computer Programming, Data Analysis, Data Management, Data Quality Assurance, Electronic Data Capture (EDC), PL/SQL (Programming Language), SQL Databases ...
Specialists, Clinical Data Management
Rahway, NJ · On-site
$87K - $137K/yr
Clinical Data Management, Communication, Computer Programming, Data Analysis, Data Management, Data Quality Assurance, Electronic Data Capture (EDC), PL/SQL (Programming Language), SQL Databases ...
Clinical Research Nurse
New Brunswick, NJ · On-site
$55 - $60/hr
Support case report form (CRF) completion and clinical trial database management * Ensure ... About Actalent Actalent is a global leader in engineering and sciences services and talent ...
Clinical Research Nurse
New Brunswick, NJ · On-site
$55 - $60/hr
Support case report form (CRF) completion and clinical trial database management * Ensure ... About Actalent Actalent is a global leader in engineering and sciences services and talent ...
Clinical Database Programmer information
See New Jersey salary details
$80.6K is the 25th percentile. Wages below this are outliers.
$70.6K - $83.7K
33% of jobs
The median wage is $94.6K / yr.
$83.7K - $96.9K
21% of jobs
$96.9K - $110K
0% of jobs
$121.1K is the 75th percentile. Wages above this are outliers.
$110K - $123.2K
25% of jobs
$123.2K - $136.3K
1% of jobs
$136.3K - $149.5K
0% of jobs
$149.5K - $162.6K
0% of jobs
$162.6K - $175.8K
0% of jobs
$175.8K - $188.9K
3% of jobs
$188.9K - $202.1K
8% of jobs
$202.1K - $215.2K
8% of jobs
$70.6K
$120.8K
$215.2K
How much do clinical database programmer jobs pay per year?
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:
- Clinical Data Assistant
- Temporary Non Clinical Chiropractic
- Clinical Feasibility
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- Director International Clinical Social Worker
- Contract Clinical Data Manager
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- Executive Director Clinical Data Management
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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:

Contractor
Re-posted 19 days ago
Job description
Artech is the 10th Largest IT Staffing Company in the US, according to Staffing Industry Analysts' 2012 annual report. Artech provides technical expertise to fill gaps in clients' immediate skill-sets availability, deliver emerging technology skill-sets, refresh existing skill base, allow for flexibility in project planning and execution phases, and provide budgeting/financial flexibility by offering contingent labor as a variable cost.
Responsibilities
Coordinate programming activities across several trials with a given compound including publication and regulatory submission activities.
Develop programming specifications for analysis datasets, pooled datasets and deliverables in consultation with the statistician.
Review and provide feedback on statistical analysis plan, output shells, CRF, edit checks and other relevant trial documents.
Develop and comply with project/study programming standards and specifications following internal guidelines
Program according to specifications, analysis datasets, pooled datasets, listings, and figures for clinical trials and submission activities
Support quality control and quality audit of deliverables
Provide input as required at all meetings, discussions and activities covering aspects of Statistical Reporting on trial level activities
Track clinical trial milestones for statistical reporting deliverables.
Maintain records for all assigned projects and archiving of trial/project analysis and associated documentation.
Maintain efficient interfaces with internal and external customers and communicate effectively across line functions.
Skills:
At least 8 years work experience in a Statistical (SAS) programming role preferably supporting clinical trials or in the pharmaceutical industry (5 years for Masters in Mathematics, Statistics/Computer Science or health science graduates).
Advanced knowledge of / experience with SAS and other relevant programming software.
Proven experience in development of advanced MACROs with high programming efficiency; strong programming and problem-solving skills.
Proven experience in leading programmer support for multiple clinical trials and submission activities (or equivalent).
Expertise in programming according to specifications of analysis datasets, pooled datasets, listings, tables and figures for clinical trials and submission activities.
Working knowledge of database design/structures and basic statistics. Working experience in pooling analysis datasets across multiple clinical studies (or equivalent).
Good understanding of global clinical trial/project practices, procedures, methodologies.
Good understanding of regulatory requirements relevant to statistical programming (e.g. GCP, ICH).
Oncology experience preferred
Strong expertise in CDISC on the submission bucket including CRT programming will be a definite plus.
Intermediate knowledge of office tools
Fluent English (oral and written)
Excellent in people interaction and be a collaborative team player.
MUST HAVE Bachelor or Master's degree in life science, computer science, statistics or equivalent relevant degree.
Regards,
Akriti Gupta
Associate Recruiter(Scientific & Clinical Division)
Artech Information Systems LLC
360 Mt. Kemble Avenue, Suite 2000 | Morristown, NJ 07960Â
Office: 973.967.3409 | Fax: 973.998.2599
Connect with us on - LinkedIn | Facebook | Twitter
About Artech
Sourced by ZipRecruiter
Artech is a leading IT staffing and consulting company based in Morristown, NJ, US. Since its foundation in 1992, Artech has mastered in complementing human expertise with technology and business acumen to produce world-class staffing solutions. The company caters to diverse industry sectors, including financial services, healthcare, telecommunication, energy and utilities, supply chain, and retail. It provides IT consulting, project management, professional and staff augmentation, and managed staffing services. Artech's mission is to provide exceptional IT staffing services to its clients by comprehending their business needs and then crafting a customized staffing strategy. Its notable achievement includes being recognized as one of the largest IT staffing companies in the U.S, according to Staffing Industry Analysts (SIA).
Industry
Recruiting and staffing services
Company size
10,000+ Employees
Headquarters location
Morristown, NJ, US
Year founded
1992