ZipRecruiter

Log In

1

Veeva Clinical Jobs (NOW HIRING)

Celerion

Veeva Clinical Database Programmer

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 ...

Celerion

Veeva Clinical Database Programmer

OR · Remote

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 ...

Celerion

Veeva Clinical Database Programmer

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 ...

United Airlines

Veeva Expert

Cincinnati, OH · On-site

$68K - $150K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Support and administer Veeva Vault Quality (QMS, Deviations, CAPA, Change Control), Veeva Vault RIM/Regulatory , and Veeva Clinical/Safety modules, where applicable. * Manage user access, security ...

United Airlines

Veeva Expert

Cincinnati, OH

$68K - $150K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Support and administer Veeva Vault Quality (QMS, Deviations, CAPA, Change Control), Veeva Vault RIM/Regulatory , and Veeva Clinical/Safety modules, where applicable. * Manage user access, security ...

United Airlines

Veeva Expert

Cincinnati, OH · On-site

$68K - $150K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Support and administer Veeva Vault Quality (QMS, Deviations, CAPA, Change Control), Veeva Vault RIM/Regulatory , and Veeva Clinical/Safety modules, where applicable. * Manage user access, security ...

Celerion

EDC Developer / Programmer

OR · Remote

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 ...

Celerion

EDC Developer / Programmer

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 ...

Celerion

EDC Developer / Programmer

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 ...

Veeva Systems

Senior Director - CTMS Strategy

They are seeking a Senior Director of Strategy to drive the adoption and growth of their Clinical Trial Management System (CTMS) within the Veeva Clinical Operations suite, focusing on market ...

Veeva Systems

Director - CTMS Strategy

The Director of Strategy will drive the adoption and growth of Veeva's Clinical Trial Management System (CTMS), focusing on market strategies and cross-functional execution to enhance clinical trial ...

Veeva Systems, Inc.

Senior Director - CTMS Strategy

Boston, MA · On-site

$150 - $300/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

The Role Veeva Systems is seeking an accomplished and driven Senior Director of Strategy to drive the adoption and growth of our Clinical Trial Management System (CTMS) within the Veeva Clinical ...

Veeva Systems, Inc.

Director - CTMS Strategy

Pleasanton, CA · On-site

$125 - $300/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

The Role Veeva Systems is seeking an accomplished and driven Director of Strategy to drive the adoption and growth of our Clinical Trial Management System (CTMS) within the Veeva Clinical Operations ...

IPolarity LLC

Program Manager

Whippany, NJ · On-site

$65 - $70/hr

Veeva Clinical expertise 3.Strong LS R&D GxP expertise JD: * Life Sciences R&D GxP experienced Global Program Manager (for client's program scope) with experience in successfully program managing a ...

next page

Showing results 1-20

All JobsVeeva Clinical Jobs

Veeva Clinical information

What is a Veeva Clinical professional?

A Veeva Clinical professional is someone who specializes in using the Veeva Vault Clinical Suite, a cloud-based platform designed to manage clinical trial processes and data in the life sciences industry. Their responsibilities often include implementing, configuring, and supporting Veeva Vault Clinical applications such as eTMF, CTMS, and Study Startup. These professionals help organizations streamline clinical operations, ensure regulatory compliance, and improve collaboration across trial teams. Their expertise is highly valued by pharmaceutical, biotech, and contract research organizations.

What are the key skills and qualifications needed to thrive as a Veeva Clinical specialist?

To thrive as a Veeva Clinical Specialist, you need a solid understanding of clinical trial processes, data management, and life sciences regulations, often supported by a degree in life sciences or related fields. Familiarity with Veeva Vault Clinical Suite, electronic data capture (EDC) systems, and relevant certifications like Veeva Vault Administrator are highly valued. Strong analytical thinking, attention to detail, and effective communication are essential soft skills for collaborating with cross-functional teams and clients. These competencies ensure the optimization of clinical workflows, regulatory compliance, and successful implementation of Veeva solutions in clinical research environments.

What are some common challenges faced by professionals working in Veeva Clinical roles, and how can they be addressed?

Professionals in Veeva Clinical roles often encounter challenges such as adapting to frequent software updates, ensuring data integrity across multiple studies, and coordinating with cross-functional teams like clinical operations and IT. Staying current with new features and best practices is essential to maximize the platform's capabilities. Proactive communication and ongoing training can help address these challenges, as well as building strong relationships with stakeholders to streamline workflows and resolve issues efficiently.
More about Veeva Clinical jobs

What cities are hiring for Veeva Clinical jobs?

Cities with the most Veeva Clinical job openings:

What states have the most Veeva Clinical jobs?

States with the most job openings for Veeva Clinical jobs include:

What job categories do people searching Veeva Clinical jobs look for?

The top searched job categories for Veeva Clinical jobs are:

Veeva Clinical jobs near you
Infographic showing various Veeva Clinical job openings in the United States as of August 2026, with employment types broken down into 3% As Needed, 72% Full Time, 17% Part Time, and 8% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution.

Veeva Clinical Database Programmer

Celerion

Remote

Full-time

Posted 11 days ago

Celerion rating

7.0

Company rating: 7.0 out of 10

Based on 13 frontline employees who took The Breakroom Quiz

62nd of 73 rated research

Job description

Celerion is committed to swift, exceptional clinical research through translational medicine.  Every day, we use our experience, agility, and innovative research strategies to help get drugs to market faster.  

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.
apply for this job

What Celerion employees say

Pay

Benefits

Hours and flexibility

Workplace

Get the full story on Breakroom

Apply