This is a full-time, remote opportunity, but you may travel for training and key meetings. As a Veeva Clinical Database Programmer , you will build and administer EDC trials for client-contracted ...
This is a full-time, remote opportunity, but you may travel for training and key meetings. As a Veeva Clinical Database Programmer , you will build and administer EDC trials for client-contracted ...
Veeva Clinical Database Programmer
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This is a full-time, remote opportunity, but you may travel for training and key meetings. As a Veeva Clinical Database Programmer , you will build and administer EDC trials for client-contracted ...
Quick apply
Veeva Clinical Database Programmer
OR · Remote
This is a full-time, remote opportunity, but you may travel for training and key meetings. As a Veeva Clinical Database Programmer , you will build and administer EDC trials for client-contracted ...
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Remote Clinical Database Programmer information
See salary details
$79.4K is the 25th percentile. Wages below this are outliers.
$69.5K - $82.5K
33% of jobs
The median wage is $93.1K / yr.
$82.5K - $95.4K
21% of jobs
$95.4K - $108.4K
0% of jobs
$119.3K is the 75th percentile. Wages above this are outliers.
$108.4K - $121.3K
25% of jobs
$121.3K - $134.3K
1% of jobs
$134.3K - $147.2K
0% of jobs
$147.2K - $160.2K
0% of jobs
$160.2K - $173.1K
0% of jobs
$173.1K - $186.1K
3% of jobs
$186.1K - $199K
8% of jobs
$199K - $212K
8% of jobs
$69.5K
$119K
$212K
How much do remote clinical database programmer jobs pay per year?
What is a remote clinical database programmer?
What is the difference between Remote Clinical Database Programmer vs Clinical Data Coordinator?
| Aspect | Remote Clinical Database Programmer | Clinical Data Coordinator |
|---|---|---|
| Credentials | Bachelor's in Life Sciences, Biostatistics, or related field; experience with database software | Bachelor's in Health Sciences, Nursing, or related field; data management experience |
| Work Environment | Remote, primarily working with database systems and programming tools | On-site or remote, managing data entry and quality control |
| Industry Usage | Pharmaceuticals, biotech, clinical research organizations |
The Remote Clinical Database Programmer focuses on designing, programming, and maintaining clinical trial databases, requiring programming skills and database expertise. In contrast, the Clinical Data Coordinator manages data collection, entry, and quality assurance. Both roles are essential in clinical research, often working together but with different technical and operational responsibilities.
What are the key skills and qualifications needed to thrive as a remote clinical database programmer?
How does a remote clinical database programmer typically collaborate with clinical teams and data managers during a clinical trial?

Celerion rating
7.0
Based on 13 frontline employees who took The Breakroom Quiz
62nd of 73 rated research
Job description
Are you looking for an opportunity to support a business creating life-saving treatments? If so, we can't wait to meet you!
We are looking for a performance-oriented, innovative and self-motivated team player to join our Clinical Data Sciences team as a full-time Veeva Clinical Database Programmer. You will be responsible for the administration of EDC database, including evaluation, analysis, design and/ or recommendations to achieve goals and excellent results in a fast-paced, ever-changing environment.
This is a full-time, remote opportunity, but you may travel for training and key meetings.
As a Veeva Clinical Database Programmer, you will build and administer EDC trials for client-contracted projects, including protocol/requirements evaluation, electronic case report form (eCRF) design and build with corresponding edits. This role will have technical interaction with vendors that are supporting the applications and troubleshoot/ escalate problems on systems to appropriate partners. This role will provide expert guidance to the design, development, validation, implementation and maintenance of study set-up. Additionally, this role will manage the deployment of EDC trials and set up interface connections between EDC and other systems.
In this role you will:
- Serve as a subject matter expert in Veeva Clinical Data Management Suite (CDMS), including Veeva Electronic Data Capture (EDC) and Veeva Clinical Database (CDB)
- Perform all activities related to eCRF design and EDC build programming for assigned projects
- Perform EDC edit check programming for assigned projects based on edit check specifications for both simple and complex edit checks
- Create test data to verify both screen design and edit check programming prior to deploying to User Acceptance Testing (UAT)
- Set up test environments and coordinate project team members for execution of test scripts
- Program and configure listings and reports using clinical reporting tools such as Veeva Clinical Database (CDB)
- Ensure secure and high-integrity database imports from vendor transfers using Celerion data transfer standards
- Assist with the validation of upgrades to hardware/ software including validation documentation development, review and execution.
- Maintain global clinical trial database standards (CDISC)
Requirements:
- Bachelor's degree in a related field preferred
- 3 years of clinical data management experience
- Ability to program using SQL required
- Experience with Veeva EDC and Veeva CDB
- Proficient computer skills with understanding of clinical systems and data administration
- Must be organized, an effective written and oral communicator
- Must have the ability to multi-task, within a fast-paced environment, and build strong relationships
#LI-Remote
Celerion Values: Integrity Trust Teamwork Respect
Celerion is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, age, sexual orientation, gender identity, genetic information, marital status, qualified protected veteran status, or disability.
Note: To make sure you don't miss important updates from us, please check your Spam folder for emails from @celerion.com, particularly interview invitations. If you find one there, mark it as "Not Junk" to ensure future Celerion emails land in your inbox. Please note that Gmail accounts have been particularly noted as routing to Spam.
We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses and identifying potential inconsistencies or verification signals in application materials based on available information. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.
About Celerion
Sourced by ZipRecruiter
Industry
Pharmaceutical and medicine manufacturing
Company size
1,001 - 5,000 Employees
Headquarters location
Lincoln, NE, US
Year founded
2010