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 ...
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 ...
Senior Specialist, Clinical Data Management - Hybrid
Rahway, NJ · Hybrid
$117K/yr
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 ...
Senior Specialist, Clinical Data Management - Hybrid
Rahway, NJ · Hybrid
$117K/yr
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 ...
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 ...
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 ...
Senior Statistical Programmer
Rahway, NJ · On-site
Clinical Database Programming, Clinical Trials, Collaborative Development, Data Modeling, Pharmaceutical Development, Project Leadership, Stakeholder Relationship Management, Statistical Programming ...
Senior Statistical Programmer
Rahway, NJ · On-site
Clinical Database Programming, Clinical Trials, Collaborative Development, Data Modeling, Pharmaceutical Development, Project Leadership, Stakeholder Relationship Management, Statistical Programming ...
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 ...
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 ...
Experience in PL/SQL, SAS, Java, C++ relational database design and database programming skills ... Clinical Data Interchange Standards Consortium (CDISC) experience. * Travel requirements * 25 ...
Experience in PL/SQL, SAS, Java, C++ relational database design and database programming skills ... Clinical Data Interchange Standards Consortium (CDISC) experience. * Travel requirements * 25 ...
The Associate Director, Clinical Data Management is responsible for providing leadership and ... Experience in PL/SQL, SAS, Java, C++ relational database design and database programming skills ...
The Associate Director, Clinical Data Management is responsible for providing leadership and ... Experience in PL/SQL, SAS, Java, C++ relational database design and database programming skills ...
Director, Clinical Data Management
Warren, NJ · On-site
Experience in PL/SQL, SAS, Java, C++ relational database design and database programming skills ... Clinical Data Interchange Standards Consortium (CDISC) experience. * Travel requirements * 25 ...
Director, Clinical Data Management
Warren, NJ · On-site
Experience in PL/SQL, SAS, Java, C++ relational database design and database programming skills ... Clinical Data Interchange Standards Consortium (CDISC) experience. * Travel requirements * 25 ...
The Associate Director, Clinical Data Management is responsible for providing leadership and ... Experience in PL/SQL, SAS, Java, C++ relational database design and database programming skills ...
The Associate Director, Clinical Data Management is responsible for providing leadership and ... Experience in PL/SQL, SAS, Java, C++ relational database design and database programming skills ...
Applied Engineering, Clinical Database Programming, Clinical Trials, Collaborative Communications, Computer Science, Data Management, Data Modeling, Innovation, Mechatronics, Numerical Analysis ...
Applied Engineering, Clinical Database Programming, Clinical Trials, Collaborative Communications, Computer Science, Data Management, Data Modeling, Innovation, Mechatronics, Numerical Analysis ...
Applied Engineering, Clinical Database Programming, Clinical Trials, Collaborative Communications, Computer Science, Data Management, Data Modeling, Innovation, Mechatronics, Numerical Analysis ...
Applied Engineering, Clinical Database Programming, Clinical Trials, Collaborative Communications, Computer Science, Data Management, Data Modeling, Innovation, Mechatronics, Numerical Analysis ...
Job Summary The Manager, EDC Database Programming is a member of the Biostatistics and Data ... clinical studies Electronic Data Capture systems and other related technologies, Clinical Data ...
Job Summary The Manager, EDC Database Programming is a member of the Biostatistics and Data ... clinical studies Electronic Data Capture systems and other related technologies, Clinical Data ...
Manager, EDC Database Programming Job Requisition ID: 1733 Posting Start Date: 7/2/26 At Daiichi ... clinical studies Electronic Data Capture systems and other related technologies, Clinical Data ...
Manager, EDC Database Programming Job Requisition ID: 1733 Posting Start Date: 7/2/26 At Daiichi ... clinical studies Electronic Data Capture systems and other related technologies, Clinical Data ...
Senior Manager, Clinical Data Systems
Florham Park, NJ · On-site
$124K/yr
Demonstrated intermediate SAS and/or SQL programming skills and expert knowledge of database concepts. * In-depth knowledge of CDASH and SDTM Standards In-depth understanding of clinical trial ...
Senior Manager, Clinical Data Systems
Florham Park, NJ · On-site
$124K/yr
Demonstrated intermediate SAS and/or SQL programming skills and expert knowledge of database concepts. * In-depth knowledge of CDASH and SDTM Standards In-depth understanding of clinical trial ...
Sr. Clinical Programmer
New York, NY · On-site
Sr. Clinical Programmer Syneos Health is a leading fully-integrated life sciences services ... Forms (CRFs), database creation, coding configuration, edit check procedures, import setup and ...
Sr. Clinical Programmer
New York, NY · On-site
Sr. Clinical Programmer Syneos Health is a leading fully-integrated life sciences services ... Forms (CRFs), database creation, coding configuration, edit check procedures, import setup and ...
Demonstrated intermediate SAS and/or SQL programming skills and expert knowledge of database concepts. * In-depth knowledge of CDASH and SDTM Standards In-depth understanding of clinical trial ...
Quick apply
Demonstrated intermediate SAS and/or SQL programming skills and expert knowledge of database concepts. * In-depth knowledge of CDASH and SDTM Standards In-depth understanding of clinical trial ...
Assistant Research Scientist - AI-Linked Cytology (P.I.: Dr. John McDevitt)
New York, NY · On-site
$55K - $65K/yr
... clinical databases essential for AI-based diagnostic model development. The successful candidate will work closely with an interdisciplinary team of scientists, clinicians, and engineers to support ...
Assistant Research Scientist - AI-Linked Cytology (P.I.: Dr. John McDevitt)
New York, NY · On-site
$55K - $65K/yr
... clinical databases essential for AI-based diagnostic model development. The successful candidate will work closely with an interdisciplinary team of scientists, clinicians, and engineers to support ...
Job Summary The Manager, EDC Database Programming is a member of the Biostatistics and Data ... clinical studies Electronic Data Capture systems and other related technologies, Clinical Data ...
Job Summary The Manager, EDC Database Programming is a member of the Biostatistics and Data ... clinical studies Electronic Data Capture systems and other related technologies, Clinical Data ...
Clinical Data Management System experience (e.g., Clintrial, Oracle Clinical) and understanding of database/programming concepts preferred. * High level of knowledge in the use of Data Management ...
Clinical Data Management System experience (e.g., Clintrial, Oracle Clinical) and understanding of database/programming concepts preferred. * High level of knowledge in the use of Data Management ...
Senior Clinical Data Manager
Bridgewater, NJ · On-site +1
$90K - $130K/yr
Participate in the database design process. Participate in EDC User Acceptance Testing (UAT ... Coordinate with programmers to complete the programming and validation of the listings and summary ...
Senior Clinical Data Manager
Bridgewater, NJ · On-site +1
$90K - $130K/yr
Participate in the database design process. Participate in EDC User Acceptance Testing (UAT ... Coordinate with programmers to complete the programming and validation of the listings and summary ...
Clinical Database Programmer information
See New York salary details
$86.9K is the 25th percentile. Wages below this are outliers.
$76K - $90.2K
33% of jobs
The median wage is $101.9K / yr.
$90.2K - $104.4K
21% of jobs
$104.4K - $118.6K
0% of jobs
$130.5K is the 75th percentile. Wages above this are outliers.
$118.6K - $132.7K
25% of jobs
$132.7K - $146.9K
1% of jobs
$146.9K - $161.1K
0% of jobs
$161.1K - $175.2K
0% of jobs
$175.2K - $189.4K
0% of jobs
$189.4K - $203.6K
3% of jobs
$203.6K - $217.8K
8% of jobs
$217.8K - $231.9K
8% of jobs
$76K
$130.1K
$231.9K
How much do clinical database programmer jobs pay per year?
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.

Full-time
Medical, Dental, Vision, Retirement, PTO
Posted 5 days ago
Job description
Job Description
Primary activities include, but are not limited to:
40% 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.
20% 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).
20% 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.
15% 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.
5% Assist clinical database manager/supervisor in project planning, manpower projections and resource allocations across therapy areas. Interface with clinical database manager/supervisor to assure consistency of technical and process strategies across all therapy areas.
Education:
A B.A. or B.S. degree, preferably in mathematics, science, a healthcare-related discipline, or computer science; or relevant skills and experience.
Required Experience and Skills:
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 years' 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.
clinicaltrialjobs
EligibleforERP
#GDMS
Required Skills:
Adaptability, Clinical Database Programming, Clinical Data Management, Clinical Programs, Clinical Research, Communication, Data Analysis, Data Quality Assurance, Data Reporting, Data Review, Data Validation, Good Clinical Practice (GCP), Medical Terminology, Project Management, TeamworkPreferred Skills:
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The salary range for this role is
$117,000.00 - $184,200.00This is the lowest to highest salary we in good faith believe we would pay for this role at the time of this posting. An employee's position within the salary range will be based on several factors including, but not limited to relevant education, qualifications, certifications, experience, skills, geographic location, government requirements, and business or organizational needs.
The successful candidate will be eligible for annual bonus and long-term incentive, if applicable.
We offer a comprehensive package of benefits. Available benefits include medical, dental, vision healthcare and other insurance benefits (for employee and family), retirement benefits, including 401(k), paid holidays, vacation, and compassionate and sick days. More information about benefits is available at https://jobs.merck.com/us/en/compensation-and-benefits.
You can apply for this role through https://jobs.merck.com/us/en (or via the Workday Jobs Hub if you are a current employee). The application deadline for this position is stated on this posting.
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